{"id":102,"date":"2021-07-05T15:36:15","date_gmt":"2021-07-05T15:36:15","guid":{"rendered":"https:\/\/aspree.org\/usa\/?page_id=102"},"modified":"2024-06-18T05:38:33","modified_gmt":"2024-06-18T05:38:33","slug":"for-clinicians","status":"publish","type":"page","link":"https:\/\/aspree.org\/usa\/for-clinicians\/","title":{"rendered":"About ASPREE for clinicians"},"content":{"rendered":"<p>[et_pb_section fb_built=&#8221;1&#8243; custom_padding_last_edited=&#8221;off|desktop&#8221; _builder_version=&#8221;4.16&#8243; background_color=&#8221;#26619A&#8221; custom_padding=&#8221;0px||0px||false|false&#8221; custom_padding_tablet=&#8221;24vh||2vh||false|false&#8221; background_color_gradient_direction_tablet=&#8221;360deg&#8221; background_color_gradient_stops_tablet=&#8221;#2b87da 49%|#29c4a9 79%&#8221; background_color_gradient_start_position_tablet=&#8221;49%&#8221; background_color_gradient_end_position_tablet=&#8221;79%&#8221; background_size_tablet=&#8221;cover&#8221; background_position_tablet=&#8221;center_right&#8221; background_position_phone=&#8221;center_right&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_row column_structure=&#8221;2_5,3_5&#8243; use_custom_gutter=&#8221;on&#8221; gutter_width=&#8221;1&#8243; make_equal=&#8221;on&#8221; custom_padding_last_edited=&#8221;on|tablet&#8221; _builder_version=&#8221;4.16&#8243; background_size=&#8221;initial&#8221; background_position=&#8221;top_left&#8221; background_repeat=&#8221;repeat&#8221; width=&#8221;100%&#8221; max_width=&#8221;100%&#8221; custom_padding=&#8221;0px||0px|4%|false|false&#8221; custom_padding_tablet=&#8221;0px|||0%|false|false&#8221; custom_padding_phone=&#8221;&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;2_5&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;30px||||false|false&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_ds_breadcrumbs module_class=&#8221;light&#8221; _builder_version=&#8221;4.5.1&#8243; _module_preset=&#8221;default&#8221; locked=&#8221;on&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_ds_breadcrumbs][et_pb_text _builder_version=&#8221;4.16&#8243; header_font=&#8221;|700|||||||&#8221; header_font_size=&#8221;42px&#8221; header_line_height=&#8221;1.15em&#8221; background_layout=&#8221;dark&#8221; width=&#8221;80%&#8221; max_width=&#8221;520px&#8221; module_alignment=&#8221;center&#8221; custom_margin=&#8221;3em||20px||false|false&#8221; custom_margin_tablet=&#8221;3em||||false|false&#8221; custom_margin_phone=&#8221;&#8221; custom_margin_last_edited=&#8221;on|desktop&#8221; header_font_size_tablet=&#8221;34px&#8221; header_font_size_phone=&#8221;24px&#8221; header_font_size_last_edited=&#8221;on|desktop&#8221; module_alignment_tablet=&#8221;&#8221; module_alignment_phone=&#8221;&#8221; module_alignment_last_edited=&#8221;on|tablet&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h1>FOR CLINICIANS<\/h1>\n<p>[\/et_pb_text][et_pb_text _builder_version=&#8221;4.16&#8243; text_font_size=&#8221;24px&#8221; background_enable_image=&#8221;off&#8221; background_layout=&#8221;dark&#8221; width=&#8221;80%&#8221; max_width=&#8221;520px&#8221; module_alignment=&#8221;center&#8221; custom_margin=&#8221;||40px||false|false&#8221; custom_padding=&#8221;||||false|false&#8221; text_font_size_tablet=&#8221;20px&#8221; text_font_size_phone=&#8221;16px&#8221; text_font_size_last_edited=&#8221;on|desktop&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<p>The ASPirin in Reducing Events in the Elderly (ASPREE) study continues to explore new ways to improve health and quality of life amongst older adults. The results will be relevant to many aging people around the world.<\/p>\n<p>[\/et_pb_text][\/et_pb_column][et_pb_column type=&#8221;3_5&#8243; _builder_version=&#8221;4.16&#8243; background_image=&#8221;https:\/\/aspree.org\/wp-content\/uploads\/sites\/3\/2021\/07\/Image-4-New-LR.jpg&#8221; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_code _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; height=&#8221;34em&#8221; height_tablet=&#8221;250px&#8221; height_phone=&#8221;250px&#8221; height_last_edited=&#8221;on|phone&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_code][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=&#8221;1&#8243; specialty=&#8221;on&#8221; padding_right_2=&#8221;0px&#8221; padding_left_2=&#8221;0px&#8221; padding_top_bottom_link_2=&#8221;false&#8221; padding_left_right_link_2=&#8221;true&#8221; module_class=&#8221;texture-left&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; inner_max_width=&#8221;80%&#8221; custom_margin=&#8221;||||false|false&#8221; custom_padding=&#8221;||90px||false|false&#8221; border_color_bottom=&#8221;#bdbec0&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;1_3&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_text admin_label=&#8221;Anchors&#8221; _builder_version=&#8221;4.16&#8243; text_font=&#8221;||||||||&#8221; text_text_color=&#8221;#26619a&#8221; header_font=&#8221;|||on|||||&#8221; header_2_font=&#8221;|||on|||||&#8221; header_2_font_size=&#8221;32px&#8221; header_3_line_height=&#8221;2em&#8221; custom_padding=&#8221;|||0px||&#8221; text_font_size_tablet=&#8221;28px&#8221; text_font_size_phone=&#8221;24px&#8221; text_font_size_last_edited=&#8221;on|phone&#8221; header_2_font_size_tablet=&#8221;28px&#8221; header_2_font_size_phone=&#8221;24px&#8221; header_2_font_size_last_edited=&#8221;on|phone&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h2>The ASPREE Project<\/h2>\n<p>&nbsp;<\/p>\n<h3>\u00a0<\/h3>\n<h3>\u2192\u00a0<a title=\"The ASPREE clinical trial (completed)\" href=\"#component1\">The ASPREE Clinical Trial (completed)\u00a0<\/a><\/h3>\n<h3>\u2192<a title=\"ASPREE clinical trial findings\" href=\"#results\"> Major ASPREE trial findings<\/a><\/h3>\n<h3>\u2192\u00a0<a title=\"The ASPREE-XT (eXTension) Follow-up Study\" href=\"#component2\">The ASPREE-XT (eXTension) Follow-up Study (ongoing)<\/a><\/h3>\n<h3>\u2192 <a title=\"Key features\" href=\"#keyfeatures\">Key features<\/a><\/h3>\n<h3>\u2192 <a title=\"Further information and FAQs\" href=\"#GPFAQs\">Further information and FAQs<\/a><\/h3>\n<p>[\/et_pb_text][\/et_pb_column][et_pb_column type=&#8221;2_3&#8243; specialty_columns=&#8221;2&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_row_inner admin_label=&#8221;PUT CONTENT BELOW AS A TEXT AND IMAGES&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; max_width=&#8221;840px&#8221; custom_padding=&#8221;|0px||0px|true|true&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;2_3&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_text admin_label=&#8221;COMPONENTS OF THE ASPREE PROJECT: Text&#8221; _builder_version=&#8221;4.20.4&#8243; _module_preset=&#8221;default&#8221; hover_enabled=&#8221;0&#8243; global_colors_info=&#8221;{}&#8221; sticky_enabled=&#8221;0&#8243;]<\/p>\n<h2>COMPONENTS OF THE ASPREE PROJECT:<\/h2>\n<ol>\n<li>A randomised, double-blind placebo controlled primary prevention trial of low-dose aspirin (ASPREE clinical trial) completed in mid-2017.<\/li>\n<li>An ongoing follow-up observational study of ASPREE participants (ASPREE-XT).<\/li>\n<\/ol>\n<h3>\u00a0<\/h3>\n<h3 id=\"component1\">ASPREE CLINICAL TRIAL\u00a0 (2010 &#8211; 2017)<\/h3>\n<p>ASPREE (ASPirin in Reducing Events in the Elderly) involved 19,114 community dwelling older adults:<\/p>\n<ul>\n<li>\u00a02,411 participants &#8211; aged 70 and older (65 years and older for minorities), and recruited from<a href=\"\/wp-content\/uploads\/sites\/3\/2021\/07\/US-ASPREE-Clinical-Trial-sites.pdf\" target=\"_blank\" rel=\"noopener noreferrer\"> 33 sites across the United States <\/a>AND<\/li>\n<li>16,703 participants &#8211; all aged 70 and older, across south eastern parts of <a title=\"link to AUS study locations\" href=\"aus\/site-locations\/\" target=\"_blank\" rel=\"noopener noreferrer\">Australia<\/a><\/li>\n<\/ul>\n<h3>Major points:<\/h3>\n<ul>\n<li>All participants were free of overt cardiovascular disease (CVD), dementia, and were otherwise healthy at enrollment.<\/li>\n<li>The primary objective was to determine whether 100 mg aspirin prolonged life free of dementia and persistent physical disability in the healthy elderly.<\/li>\n<li>The trial also examined whether low-dose aspirin affected cancer, clinically significant bleeding, dementia, heart failure, myocardial infarction, physical disability, stroke\/TIA, and depression.<\/li>\n<li>The median intervention time period was 4.7 years.<\/li>\n<\/ul>\n<h3 id=\"results\">Findings:<\/h3>\n<p>The principal results of ASPREE were published in the <em>New England Journal of Medicine<\/em> in 2018. These provided the first high quality findings on the value of low-dose aspirin for primary prevention in healthy older adults, mostly aged 70 and over.<\/p>\n<ul>\n<li>Aspirin did not prolong healthy life span free of dementia and persistent physical disability (<a title=\"Link to NEJM - Disability Free Survival ASPREE paper\" href=\"https:\/\/www.nejm.org\/doi\/full\/10.1056\/NEJMoa1800722\" target=\"_blank\" rel=\"noopener noreferrer\">McNeil\u00a0<em>et al<\/em>. 2018<\/a>).<\/li>\n<li>Mortality was slightly higher in the aspirin group than in the placebo group (5.9% aspirin: 5.7% placebo),\u00a0attributed primarily to cancer-related deaths (<a title=\"Link to NEJM - All cause mortality ASPREE paper\" href=\"https:\/\/www.nejm.org\/doi\/full\/10.1056\/nejmoa1803955\" target=\"_blank\" rel=\"noopener noreferrer\">McNeil\u00a0<em>et al<\/em>. 2018<\/a>).<\/li>\n<li>Aspirin did not significantly reduce the risk of heart disease or stroke.<\/li>\n<li>Aspirin significantly increased the risk of bleeding, primarily intracranial and in the GIT\u00a0 (<a title=\"Link to NEJM - CVD &amp; Bleeding ASPREE paper\" href=\"https:\/\/www.nejm.org\/doi\/full\/10.1056\/nejmoa1805819\" target=\"_blank\" rel=\"noopener noreferrer\">McNeil <em>et al<\/em>. 2018<\/a>).<\/li>\n<\/ul>\n<p>Media announcement of the trial&#8217;s results can be viewed <a title=\"NIA ASPREE findings media release \" href=\"\/wp-content\/uploads\/sites\/2\/2020\/09\/NIH-PRESS-RELEASE-ASPREE-NEJM09.2018.pdf\" target=\"_blank\" rel=\"attachment wp-att-1355 noopener noreferrer\">here<\/a>.<\/p>\n<p>A series of additional reports have been published describing the impact of low- dose aspirin on other conditions including depression, cognitive decline and sepsis. These can be accessed <a title=\"link to ASPREE publications\" href=\"\/aus\/publications\/\" target=\"_blank\" rel=\"noopener noreferrer\">here.<\/a><\/p>\n<p>Prominent\u00a0<a title=\"AHA\/ACC aspirin prevention guidelines\" href=\"https:\/\/www.jacc.org\/doi\/full\/10.1016\/j.jacc.2019.03.009\" target=\"_blank\" rel=\"noopener noreferrer\">US guidelines<\/a> incorporated ASPREE findings, recommending against routine use of aspirin for primary prevention in healthy adults aged 70 and older.<\/p>\n<blockquote>\n<p>\u201cFor a large fraction of our professional lives, we have been telling patients who suffered from a prior major cardiovascular event, such as myocardial infarction or stroke, that daily ingestion of about 82 mg of aspirin a day could help protect against further events. Since the intervention was perceived to have few side effects, many of us advised previously healthy older adults to take a daily low-dose aspirin to protect against cardiovascular disease. This daily regimen was inexpensive, low-risk \u2014 or so we thought \u2014 and appeared to provide a benefit. But a trio of studies published last September found that a daily aspirin doesn\u2019t do much good, and may even cause harm,\u201d <a href=\"https:\/\/www.hhrinstitute.org\/aspree-study-a-game-changer-at-the-cutting-edge-of-medicine\/\" target=\"_blank\" rel=\"noopener noreferrer\">wrote Jeffrey M. Drazen, MD, Editor-in-Chief of the\u00a0<em>New England Journal of Medicine.<\/em>\u2019<\/a><\/p>\n<\/blockquote>\n<h3>\u00a0<\/h3>\n<h3 id=\"component2\">ASPREE-XT (eXTension) FOLLOW-UP STUDY (2017 &#8211; 2024)<\/h3>\n<ul>\n<li>Most participants of the ASPREE trial are continuing to be followed in person or through their medical records. This extension, known as ASPREE-XT, is an observational study of health outcomes in older adults.<\/li>\n<li>The primary objective is to determine whether there are delayed (legacy) effects of daily 100 mg aspirin treatment, particularly on the incidence and mortality from bowel cancer.<\/li>\n<li>An additional objective is to study the impact of various lifestyle, environmental and genomic factors on the physical and cognitive health of older adults.<\/li>\n<li>Involves annual collection of clinical, neurocognitive and physical function measures, mood, quality of life, physical ability, demographic and lifestyle details, pathology (Plasma\/Serum Cr, HbA1c, Complete Blood Count (CBC), Hb, uACR).<\/li>\n<\/ul>\n<p>Details of relevant clinical events are sourced from medical records. Participant health outcomes are adjudicated on evidence provided by medical records.<\/p>\n<h3>\u00a0<\/h3>\n<h3>Funding<\/h3>\n<p>The ASPREE project is <a href=\"\/usa\/about-us\/funding-and-collaborators\/\">funded<\/a> by the <a title=\"NIA website\" href=\"https:\/\/www.nia.nih.gov\/\" target=\"_blank\" rel=\"noopener noreferrer\">National Institute on Aging<\/a>\u00a0and the\u00a0<a title=\"NCI website\" href=\"https:\/\/www.cancer.gov\/\" target=\"_blank\" rel=\"noopener noreferrer\">National Cancer Institute<\/a>\u00a0(NIA and NCI; both part of the US National Institutes of Health) the\u00a0<a title=\"NHMRC website\" href=\"https:\/\/www.nhmrc.gov.au\/\" target=\"_blank\" rel=\"noopener noreferrer\">National Health and Medical Research Council of Australia<\/a>, <a href=\"https:\/\/www.victoriancanceragency.vic.gov.au\/\" target=\"_blank\" rel=\"noopener noreferrer\">Victorian Cancer Agency<\/a> and <a title=\"Monash University website\" href=\"https:\/\/www.monash.edu\/\" target=\"_blank\" rel=\"noopener noreferrer\">Monash University<\/a>.<\/p>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][\/et_pb_column][\/et_pb_section][et_pb_section fb_built=&#8221;1&#8243; _builder_version=&#8221;4.16&#8243; background_color=&#8221;#26619a&#8221; background_image=&#8221;https:\/\/aspree.org\/wp-content\/uploads\/sites\/3\/2021\/07\/texture-2.png&#8221; background_size=&#8221;initial&#8221; background_position=&#8221;top_right&#8221; background_blend=&#8221;overlay&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_row _builder_version=&#8221;4.16&#8243; background_size=&#8221;initial&#8221; background_position=&#8221;top_left&#8221; background_repeat=&#8221;repeat&#8221; custom_padding=&#8221;0px||0px||true|false&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;4_4&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_text admin_label=&#8221;Key features HEADER&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;d100a70a-4a1b-4c0a-852d-deb7ebdb8d36&#8243; header_font=&#8221;|600||on|||||&#8221; header_text_align=&#8221;left&#8221; header_2_font=&#8221;|600||on|||||&#8221; header_2_text_align=&#8221;left&#8221; header_2_font_size=&#8221;32px&#8221; text_orientation=&#8221;center&#8221; background_layout=&#8221;dark&#8221; custom_margin=&#8221;||0px||false|false&#8221; header_2_font_size_tablet=&#8221;28px&#8221; header_2_font_size_phone=&#8221;24px&#8221; header_2_font_size_last_edited=&#8221;on|desktop&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h2 id=\"keyfeatures\">Key features <\/h2>\n<p>[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=&#8221;1_3,1_3,1_3&#8243; use_custom_gutter=&#8221;on&#8221; make_equal=&#8221;on&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;1_3&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;5fc07e0a-53a2-4b20-aac9-883fa2ab9fbb&#8221; background_color=&#8221;#ffffff&#8221; box_shadow_style=&#8221;preset1&#8243; box_shadow_blur=&#8221;8px&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_code admin_label=&#8221;Image (as background)&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; background_image=&#8221;https:\/\/aspree.org\/wp-content\/uploads\/sites\/3\/2021\/07\/USA1.jpg&#8221; width=&#8221;100%&#8221; height=&#8221;220px&#8221; custom_margin=&#8221;0px||0px||true|false&#8221; custom_padding=&#8221;0px||0px||true|false&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_code][et_pb_text admin_label=&#8221;Text&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; text_line_height=&#8221;1.8em&#8221; header_2_font=&#8221;|600|||||||&#8221; header_4_text_align=&#8221;center&#8221; background_color=&#8221;#ffffff&#8221; custom_margin=&#8221;0px||0px||true|false&#8221; custom_padding=&#8221;5%|5%|5%|5%|true|true&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3><strong>ASPREE Features<\/strong><\/h3>\n<ul>\n<li>Largest United States\/Australian collaborative randomized clinical trial yet reported<\/li>\n<li><a href=\"\/usa\/about-us\/funding-and-collaborators\">Multiple<\/a> universities, institutions, and teaching hospitals<\/li>\n<li>100% publicly funded research<\/li>\n<li>Contributed to revised <a href=\"https:\/\/www.jacc.org\/doi\/full\/10.1016\/j.jacc.2019.03.009\" target=\"_blank\" rel=\"noopener noreferrer\">primary prevention aspirin guidelines<\/a><\/li>\n<\/ul>\n<p>[\/et_pb_text][\/et_pb_column][et_pb_column type=&#8221;1_3&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;5fc07e0a-53a2-4b20-aac9-883fa2ab9fbb&#8221; background_color=&#8221;#ffffff&#8221; box_shadow_style=&#8221;preset1&#8243; box_shadow_blur=&#8221;8px&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_code admin_label=&#8221;Image (as background)&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; background_image=&#8221;https:\/\/aspree.org\/wp-content\/uploads\/sites\/3\/2021\/07\/hal-gatewood-iPl3q-gEGzY-unsplashcrop.jpg&#8221; width=&#8221;100%&#8221; height=&#8221;220px&#8221; custom_margin=&#8221;0px||0px||true|false&#8221; custom_padding=&#8221;0px||0px||true|false&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_code][et_pb_text admin_label=&#8221;Text&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; text_line_height=&#8221;1.8em&#8221; header_2_font=&#8221;|600|||||||&#8221; header_4_text_align=&#8221;center&#8221; background_color=&#8221;#ffffff&#8221; custom_margin=&#8221;0px||0px||true|false&#8221; custom_padding=&#8221;5%|5%|5%|5%|true|true&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3><strong>ASPREE publications in NEJM<\/strong><\/h3>\n<p><strong>Published September 18, 2018<\/strong><\/p>\n<ul>\n<li><a href=\"https:\/\/www.nejm.org\/doi\/full\/10.1056\/NEJMoa1800722?query=featured_home\" target=\"_blank\" rel=\"noopener noreferrer\">Effect of Aspirin on Disability-free Survival in the Healthy Elderly (primary paper)<\/a><\/li>\n<li><a href=\"https:\/\/www.nejm.org\/doi\/full\/10.1056\/NEJMoa1803955?query=featured_home\" target=\"_blank\" rel=\"noopener noreferrer\">Effect of Aspirin on All-Cause Mortality in the Healthy Elderly<\/a><\/li>\n<li><a href=\"https:\/\/www.nejm.org\/doi\/full\/10.1056\/NEJMoa1805819?query=featured_home\" target=\"_blank\" rel=\"noopener noreferrer\">Effect of Aspirin on Cardiovascular Events and Bleeding in the Healthy Elderly<\/a><\/li>\n<\/ul>\n<p>[\/et_pb_text][\/et_pb_column][et_pb_column type=&#8221;1_3&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;5fc07e0a-53a2-4b20-aac9-883fa2ab9fbb&#8221; background_color=&#8221;#ffffff&#8221; box_shadow_style=&#8221;preset1&#8243; box_shadow_blur=&#8221;8px&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_code admin_label=&#8221;Image (as background)&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; background_image=&#8221;https:\/\/aspree.org\/wp-content\/uploads\/sites\/3\/2021\/07\/022_knee-MRI_359292copyrightMonash.jpg&#8221; width=&#8221;100%&#8221; height=&#8221;220px&#8221; custom_margin=&#8221;0px||0px||true|false&#8221; custom_padding=&#8221;0px||0px||true|false&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_code][et_pb_text admin_label=&#8221;Text&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; text_line_height=&#8221;1.8em&#8221; header_2_font=&#8221;|600|||||||&#8221; header_4_text_align=&#8221;center&#8221; background_color=&#8221;#ffffff&#8221; custom_margin=&#8221;0px||0px||true|false&#8221; custom_padding=&#8221;5%|5%|5%|5%|true|true&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3><strong>ASPREE Sub-studies<\/strong><\/h3>\n<p>ASPREE embedded a large number of additional<a title=\"link to sub-studies page\" href=\"\/usa\/sub-studies\/\"> sub-studies<\/a> exploring whether low-dose aspirin affected various aspects of health including: hearing loss, age-related macular degeneration, falls and fractures, cancer, sepsis, microbiome and more!<\/p>\n<p>&nbsp;<\/p>\n<p>[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=&#8221;1&#8243; specialty=&#8221;on&#8221; admin_label=&#8221;TABBED CONTENT (LIGHT)&#8221; module_id=&#8221;scroll_tab1&#8243; module_class=&#8221;tabs&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; inner_max_width=&#8221;80%&#8221; custom_margin=&#8221;||||false|false&#8221; custom_padding=&#8221;||90px||false|false&#8221; border_width_bottom=&#8221;1px&#8221; border_color_bottom=&#8221;#bdbec0&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;1_3&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_text _builder_version=&#8221;4.16&#8243; text_text_color=&#8221;#26619a&#8221; header_2_font=&#8221;||||||||&#8221; header_2_font_size=&#8221;32px&#8221; header_3_font=&#8221;|600|||||||&#8221; custom_margin=&#8221;||0px||false|false&#8221; custom_padding=&#8221;||0px||false|false&#8221; header_2_font_size_tablet=&#8221;28px&#8221; header_2_font_size_phone=&#8221;24px&#8221; header_2_font_size_last_edited=&#8221;on|desktop&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3 id=\"GPFAQs\">Further information for clinicians<\/strong><\/h3>\n<p>Select question below<\/p>\n<p>&nbsp;<\/p>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;DO NOT DELETE&#8221; module_class=&#8221;tab-link&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; link_text_color=&#8221;#2F2F2F&#8221; custom_margin=&#8221;||||false|false&#8221; custom_padding=&#8221;0px||0px||false|false&#8221; locked=&#8221;on&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_text][et_pb_text admin_label=&#8221;What does the ASPREE-XT study involve?&#8221; module_class=&#8221;tab-link&#8221; _builder_version=&#8221;4.19.3&#8243; _module_preset=&#8221;default&#8221; link_text_color=&#8221;#2F2F2F&#8221; custom_margin=&#8221;||||false|false&#8221; custom_padding=&#8221;0.5em||0.5em||true|false&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<p><a href=\"#\">What does the ASPREE-XT study involve?<\/a><\/p>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;Implications clinical practice&#8221; module_class=&#8221;tab-link&#8221; _builder_version=&#8221;4.19.3&#8243; _module_preset=&#8221;default&#8221; link_text_color=&#8221;#2F2F2F&#8221; custom_margin=&#8221;||||false|false&#8221; custom_padding=&#8221;0.5em||0.5em||true|false&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<p><a href=\"#\">What are the implications of ASPREE results for clinical practice?<\/a><\/p>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;cancer outcomes&#8221; module_class=&#8221;tab-link&#8221; _builder_version=&#8221;4.19.3&#8243; _module_preset=&#8221;default&#8221; link_text_color=&#8221;#2F2F2F&#8221; custom_margin=&#8221;||||false|false&#8221; custom_padding=&#8221;0.5em||0.5em||true|false&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<p><a href=\"#\">Why is ASPREE and ASPREE-XT looking at cancer outcomes?<\/a><\/p>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;what happens cog decline&#8221; module_class=&#8221;tab-link&#8221; _builder_version=&#8221;4.19.3&#8243; _module_preset=&#8221;default&#8221; link_text_color=&#8221;#2F2F2F&#8221; custom_margin=&#8221;||||false|false&#8221; custom_padding=&#8221;0.5em||0.5em||true|false&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<p><a href=\"#\">What happens when a patient may have cognitive decline?<\/a><\/p>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;collection medical records&#8221; module_class=&#8221;tab-link&#8221; _builder_version=&#8221;4.19.3&#8243; _module_preset=&#8221;default&#8221; link_text_color=&#8221;#2F2F2F&#8221; custom_margin=&#8221;||||false|false&#8221; custom_padding=&#8221;0.5em||0.5em||true|false&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<p><a href=\"#\">How does ASPREE collect participant medical records?<\/a><\/p>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;what happens &#8211; study endpoint? &#8221; module_class=&#8221;tab-link&#8221; _builder_version=&#8221;4.19.3&#8243; _module_preset=&#8221;default&#8221; link_text_color=&#8221;#2F2F2F&#8221; custom_margin=&#8221;||||false|false&#8221; custom_padding=&#8221;0.5em||0.5em||true|false&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<p><a href=\"#\">What happens when patients reach a study endpoint?<\/a><\/p>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;FAQ TAB TITLE&#8221; module_class=&#8221;tab-link&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; link_text_color=&#8221;#2F2F2F&#8221; custom_margin=&#8221;||||false|false&#8221; custom_padding=&#8221;0.5em||0.5em||true|false&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<p><a href=\"#\">What sub-studies were incorporated into the ASPREE project?<\/a><\/p>\n<p>[\/et_pb_text][et_pb_divider _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; custom_margin=&#8221;1em||-1em||false|false&#8221; custom_padding=&#8221;0px||0px||false|false&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_divider][et_pb_text admin_label=&#8221;XT protocol&#8221; module_class=&#8221;tab-link&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; link_text_color=&#8221;#2F2F2F&#8221; custom_margin=&#8221;||||false|false&#8221; custom_padding=&#8221;0.5em||0.5em||true|false&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<p><a href=\"#\">ASPREE-XT Study Protocol<\/a><\/p>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;Trial protocol&#8221; module_class=&#8221;tab-link&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; link_text_color=&#8221;#2F2F2F&#8221; custom_margin=&#8221;||||false|false&#8221; custom_padding=&#8221;0.5em||0.5em||true|false&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<p><a href=\"#\">ASPREE Clinical Trial Protocol<\/a><\/p>\n<p>[\/et_pb_text][\/et_pb_column][et_pb_column type=&#8221;2_3&#8243; specialty_columns=&#8221;2&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;|||&#8221; global_colors_info=&#8221;{}&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_row_inner _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; custom_margin=&#8221;||0px||false|false&#8221; custom_padding=&#8221;||0px||false|false&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;2_3&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_divider divider_weight=&#8221;6px&#8221; disabled_on=&#8221;off|off|on&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; custom_margin=&#8221;||0px||false|false&#8221; custom_padding=&#8221;||||false|false&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_divider][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner admin_label=&#8221;FAQ TAB CONTENT&#8221; module_id=&#8221;scroll_tab2&#8243; module_class=&#8221;tab-content&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; max_width=&#8221;840px&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;2_3&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.16&#8243; header_2_font=&#8221;|600|||||||&#8221; header_2_font_size=&#8221;32px&#8221; header_2_font_size_tablet=&#8221;28px&#8221; header_2_font_size_phone=&#8221;24px&#8221; header_2_font_size_last_edited=&#8221;on|desktop&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h2>Frequently asked questions<\/h2>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;what project involves&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; text_text_color=&#8221;#000000&#8243; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3><strong>Q: What does the ASPREE\/ASPREE-XT study involve?<\/strong><\/h3>\n<p><strong>A:<\/strong>\u00a0ASPREE-XT is conducted similarly\u00a0to the ASPREE clinical trial, but participants are no longer taking study tablets (100mg aspirin or a matched placebo).<\/p>\n<h4>\u00a0<\/h4>\n<h4>Your role in ASPREE-XT<\/h4>\n<ul>\n<li>Oversee your patients\u2019 routine health care, including pathology. Patients do not take study tablets in ASPREE-XT.<\/li>\n<li>Receive a summary of your patient\u2019s clinical and performance measures (e.g. cognitive changes, BP, weight, CESD-10, etc.) detected at ASPREE-XT study visits.<\/li>\n<li>As a co-investigator to ASPREE-XT, you are acknowledged for your contribution to significant public health research.<\/li>\n<li>You will be sent updates on the progress of ASPREE-XT and ASPREE publications.<\/li>\n<\/ul>\n<h4>\u00a0<\/h4>\n<h4>Your patient\u2019s role in ASPREE-XT<\/h4>\n<ul>\n<li>Most ASPREE participants expressed a desire to continue in the follow-up ASPREE-XT study.<\/li>\n<li>Your ASPREE-XT patients have given consent to access their medical records, receive phone calls every 6 months, and attend face-to-face annual study visits with our research staff.<\/li>\n<li>Your patient undertakes clinical, neurocognitive and physical function measurements, pathology, and completes questionnaires for mood, quality of life, physical ability, and provides personal health, demographic, and lifestyle details.<\/li>\n<li>Medical records provide critical data for ASPREE-XT researchers to accurately adjudicate patient health outcomes for inclusion in the analysis.<\/li>\n<\/ul>\n<p>Primary Care Providers (PCPs) and research staff reinforce the importance of the ASPREE study. We acknowledge their contributions and dedication to this significant research.<\/p>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner admin_label=&#8221;FAQ TAB CONTENT&#8221; module_id=&#8221;scroll_tab2&#8243; module_class=&#8221;tab-content&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; max_width=&#8221;840px&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;2_3&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.16&#8243; header_2_font=&#8221;|600|||||||&#8221; header_2_font_size=&#8221;32px&#8221; header_2_font_size_tablet=&#8221;28px&#8221; header_2_font_size_phone=&#8221;24px&#8221; header_2_font_size_last_edited=&#8221;on|desktop&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h2>Frequently asked questions<\/h2>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;Implications for practice &#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; text_text_color=&#8221;#000000&#8243; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3><strong>Q: What are the implications of ASPREE findings for clinical practice?<\/strong><\/h3>\n<p>&nbsp;<\/p>\n<ul>\n<li>Results from the ASPREE trial are applicable to <strong>ONLY<\/strong> primary prevention.<\/li>\n<li>PRIMARY PREVENTION \u2013 <em>Primary prevention aims to prevent disease or injury before it occurs, by preventing exposures to hazards, altering unhealthy or unsafe behaviors and increasing resistance to disease or injury upon exposure.<\/em><\/li>\n<li>90% of the participants in ASPREE were not regular aspirin users. Therefore, strictly, the ASPREE results apply most clearly to those initiating aspirin for the first time. The advice about whether to continue low-dose aspirin in a person who has been taking it regularly for some time is uncertain.<\/li>\n<li>The use of low-dose aspirin for secondary prevention (after a myocardial infarction, stroke, angina, TIA, etc.) is much better established and should <a href=\"https:\/\/jamanetwork.com\/journals\/jama\/fullarticle\/2761090\" target=\"_blank\" rel=\"noopener noreferrer\">continue<\/a>.<\/li>\n<\/ul>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner admin_label=&#8221;FAQ TAB CONTENT&#8221; module_id=&#8221;scroll_tab2&#8243; module_class=&#8221;tab-content&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; max_width=&#8221;840px&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;2_3&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.16&#8243; header_2_font=&#8221;|600|||||||&#8221; header_2_font_size=&#8221;32px&#8221; header_2_font_size_tablet=&#8221;28px&#8221; header_2_font_size_phone=&#8221;24px&#8221; header_2_font_size_last_edited=&#8221;on|desktop&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h2>Frequently asked questions<\/h2>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;Cancer outcomes&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; text_text_color=&#8221;#000000&#8243; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3><strong>Q: Why are ASPREE and ASPREE-XT looking at cancer outcomes?<\/strong><\/h3>\n<h5><em>Meta-analyses published in The Lancet by other researchers such as Rothwell et al. provided evidence in support of low-dose aspirin preventing cancers of the colon, oesophagus, lung and stomach.<\/em><\/h5>\n<p>&nbsp;<\/p>\n<p><strong>A:\u00a0<\/strong>ASPREE <a href=\"https:\/\/www.nejm.org\/doi\/full\/10.1056\/nejmoa1803955\" target=\"_blank\" rel=\"noopener noreferrer\">reported<\/a> a slightly higher death rate amongst the aspirin-treated group than in those taking placebo.\u00a0 It was mostly explained by more rapid progress of cancers that were already advanced when they were <a href=\"https:\/\/academic.oup.com\/jnci\/advance-article\/doi\/10.1093\/jnci\/djaa114\/5889955\" target=\"_blank\" rel=\"noopener noreferrer\">diagnosed<\/a>.<\/p>\n<p>This finding was based on small numbers and could have occurred by chance. Also, in many previous aspirin trials, no similar findings were observed and there was considerable evidence suggesting that aspirin may lead to a reduction in cancer.<\/p>\n<p>However, studies that have described a reduction in cancer mortality (particularly colorectal cancer mortality) have found that the effect starts to appear only 5-10 years after a period of prolonged intake of aspirin. Mostly these findings have originated from studies in younger populations.<\/p>\n<p>At present the existence of a cancer-reducing effect of aspirin is <a href=\"https:\/\/academic.oup.com\/jnci\/advance-article\/doi\/10.1093\/jnci\/djab010\/6123750\" target=\"_blank\" rel=\"noopener noreferrer\">controversial, especially since the findings of ASPREE were published.<\/a> The continued follow-up of ASPREE participants after a median 4.7 years of intervention will determine whether the early increase in cancer mortality is followed by a later decline.<\/p>\n<p>View selected cancer papers <a title=\"link to select cancer papers\" href=\"\/wp-content\/uploads\/sites\/3\/2021\/07\/Selected-references-aspirin-and-cancer-15.02.2021.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">here<\/a>.<\/p>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner admin_label=&#8221;FAQ TAB CONTENT&#8221; module_id=&#8221;scroll_tab2&#8243; module_class=&#8221;tab-content&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; max_width=&#8221;840px&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;2_3&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.16&#8243; header_2_font=&#8221;|600|||||||&#8221; header_2_font_size=&#8221;32px&#8221; header_2_font_size_tablet=&#8221;28px&#8221; header_2_font_size_phone=&#8221;24px&#8221; header_2_font_size_last_edited=&#8221;on|desktop&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h2>Frequently asked questions<\/h2>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;Cog decline&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; text_text_color=&#8221;#000000&#8243; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3><strong>Q:\u00a0<\/strong><strong>What happens when your patient may have cognitive decline?<\/strong><\/h3>\n<p><strong>A:\u00a0 <\/strong>At every annual study visit, our research staff track the cognitive state of study participants by administering the Modified Mini-Mental State (3MS); an internationally accepted neuro-cognitive screening tool that uses a 100-point scale. The 3MS is more sensitive to cognitive change than the MMSE, which uses a 30-point scale.<\/p>\n<p>If a participant\u2019s 3MS score declines to a predetermined level (set by population normative data) at any point during the study then:<strong><br \/><\/strong><\/p>\n<ul>\n<li>The participant is invited to undertake further cognitive measures with specially trained ASPREE research staff.<\/li>\n<li>ASPREE staff will notify the participant\u2019s PCP of the 3MS decline and recommend further follow-up such as referral for specialist or assessment clinic review, brain imaging, and dementia screening pathology.<\/li>\n<\/ul>\n<p>Subsequently:<\/p>\n<ul>\n<li>Findings from additional cognitive measures are provided to the participant\u2019s PCP and if a specialist referral is not appropriate or possible, the PCP\/specialist will be asked to provide a clinical opinion on a short questionnaire (DSM-IV proforma).<\/li>\n<li>ASPREE staff seek medical documentation relevant to dementia investigations from medical practices, specialists and assessment clinics.<\/li>\n<li>Findings from routine cognitive measures (i.e. 3MS) and the specialized cognitive review, dementia investigative reports and the PCP completed DSM-IV proforma (if available) are then collated and form the basis for specialist adjudication on whether the participant has reached a dementia \u2018endpoint\u2019 during the ASPREE-XT study period.<\/li>\n<\/ul>\n<p>ASPREE does not initiate clinical assessment or treatment of cognitive decline. The literature highlights the value of early diagnosis of dementia, as there are now effective interventions that may improve patient quality of life. Recent research also shows a reversible cause may be present in some cases.<\/p>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner admin_label=&#8221;FAQ TAB CONTENT&#8221; module_id=&#8221;scroll_tab2&#8243; module_class=&#8221;tab-content&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; max_width=&#8221;840px&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;2_3&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.16&#8243; header_2_font=&#8221;|600|||||||&#8221; header_2_font_size=&#8221;32px&#8221; header_2_font_size_tablet=&#8221;28px&#8221; header_2_font_size_phone=&#8221;24px&#8221; header_2_font_size_last_edited=&#8221;on|desktop&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h2>Frequently asked questions<\/h2>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;medical records&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; text_text_color=&#8221;#000000&#8243; custom_padding=&#8221;4px|||||&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3><strong>Q:\u00a0<\/strong><strong>How does ASPREE collect participant medical records?<\/strong><\/h3>\n<p>All study participants have consented for trained ASPREE staff members to review their medical records and collect documentation of clinical events from their Primary Care Provider (PCP), specialist and hospital.<\/p>\n<p>Medical records provide the documentation necessary for ASPREE investigators with the relevant clinical expertise, to adjudicate whether a participant has reached a predetermined study \u2018endpoint\u2019, such as cancer or dementia. This process is critical to the project\u2019s findings and maintenance of high-quality data.<\/p>\n<p>Our research staff use key terms to search medical records for evidence of clinical health events\u00a0studied in the ASPREE project. For instance, key search terms used to identify stroke events include &#8216;stroke,&#8217; &#8216;CVA&#8217;, &#8216;cerebrovascular accident,&#8217; and &#8216;cerebral infarct.&#8217;\u00a0\u00a0<\/p>\n<p>PCPs are always welcome to proactively advise ASPREE of their patient\u2019s clinical event, however, we understand that most practices are too busy. Our trained staff securely and confidentially collect this information when they review the participant\u2019s medical record.\u00a0<\/p>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner admin_label=&#8221;FAQ TAB CONTENT&#8221; module_id=&#8221;scroll_tab2&#8243; module_class=&#8221;tab-content&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; max_width=&#8221;840px&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;2_3&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.16&#8243; header_2_font=&#8221;|600|||||||&#8221; header_2_font_size=&#8221;32px&#8221; header_2_font_size_tablet=&#8221;28px&#8221; header_2_font_size_phone=&#8221;24px&#8221; header_2_font_size_last_edited=&#8221;on|desktop&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h2>Frequently asked questions<\/h2>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;study endpoint&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; text_text_color=&#8221;#000000&#8243; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3><strong>Q: What happens when patients reach a study endpoint?<\/strong><\/h3>\n<p><strong>A: <\/strong>We ask all participants to continue in the follow-up ASPREE-XT Study, attending scheduled study visits where ever possible. Tracking the ongoing health of each participant after a study endpoint is pivotal.<\/p>\n<p>All health data from ASPREE participants collected for the duration of the project greatly contribute to the study\u2019s quality and findings.<strong><br \/><\/strong><\/p>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner admin_label=&#8221;FAQ TAB CONTENT&#8221; module_id=&#8221;scroll_tab2&#8243; module_class=&#8221;tab-content&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; max_width=&#8221;840px&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;2_3&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.16&#8243; header_2_font=&#8221;|600|||||||&#8221; header_2_font_size=&#8221;32px&#8221; header_2_font_size_tablet=&#8221;28px&#8221; header_2_font_size_phone=&#8221;24px&#8221; header_2_font_size_last_edited=&#8221;on|desktop&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h2>Frequently asked questions<\/h2>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;sub-studies&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; text_text_color=&#8221;#000000&#8243; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3><strong>Q: What sub-studies were incorporated into the ASPREE project?<\/strong><\/h3>\n<p><strong>A: <\/strong>Large-scale research projects take many years and costs tens of millions of dollars.\u00a0Because of the cost and the logistics, such studies are infrequently undertaken. ASPREE was a rare opportunity to undertake many ancillary studies to provide important public health information. Study participants largely found sub-studies interesting and engaging. View ASPREE sub-studies <a title=\"link to ASPREE sub-studies\" href=\"\/usa\/sub-studies\/\" target=\"_blank\" rel=\"noopener noreferrer\">here<\/a>.<\/p>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner admin_label=&#8221;DIVIDER FROM FAQ&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; custom_margin=&#8221;0px||0px||true|false&#8221; custom_padding=&#8221;0px||0px||true|false&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;2_3&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_divider show_divider=&#8221;off&#8221; admin_label=&#8221;DO NOT DELETE&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; custom_margin=&#8221;0px||0px||true|false&#8221; custom_padding=&#8221;0px||0px||true|false&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_divider][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner admin_label=&#8221;TAB CONTENT&#8221; module_class=&#8221;tab-content&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; max_width=&#8221;840px&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;2_3&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.16&#8243; header_2_font=&#8221;|600|||||||&#8221; header_2_font_size=&#8221;32px&#8221; header_2_font_size_tablet=&#8221;28px&#8221; header_2_font_size_phone=&#8221;24px&#8221; header_2_font_size_last_edited=&#8221;on|desktop&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h2>ASPREE-XT Study Protocol<\/h2>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;XT protocol&#8221; _builder_version=&#8221;4.20.4&#8243; _module_preset=&#8221;default&#8221; text_text_color=&#8221;#000000&#8243; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3>Summary<\/h3>\n<p>ASPREE-XT is a longitudinal, observational follow-up study of ASPREE participants to determine whether there are long-lasting (legacy) effects of a median 4.7 years of treatment with daily low-dose aspirin on the key outcome measures of:<\/p>\n<p>1) Cancer, metastases and cancer mortality<br \/>2) The composite primary ASPREE-XT outcome of dementia, disability or death<br \/>3) Secondary ASPREE-XT outcomes of all-cause mortality, dementia, physical disability, cancer, mild cognitive impairment, depression and frailty, incidence of cardiovascular disease including fatal and non-fatal stroke, major hemorrhage.<\/p>\n<ul>\n<li>An additional objective is to study the impact of demographic, comorbid, environmental and genomic factors on the maintenance of cognition and other aspects of health amongst older adults.<\/li>\n<li>Study methodology is based closely on the ASPREE clinical trial.<\/li>\n<li>Involves annual data collection of clinical, neurocognitive and physical function measures, mood, quality of life, physical ability, demographic and lifestyle details, pathology (FBE, HbA1c, creatinine, ACR) and\/or clinical events via medical records.<\/li>\n<li>ASPREE-XT is funded by the\u00a0<a href=\"http:\/\/www.nia.nih.gov\/\" target=\"_blank\" rel=\"noopener noreferrer\" data-saferedirecturl=\"https:\/\/www.google.com\/url?q=http:\/\/www.nia.nih.gov\/&amp;source=gmail&amp;ust=1613628187106000&amp;usg=AFQjCNFjhAezSnFQ6YbXK0hf6WD2KTDziA\">National Institute on Aging\u00a0<\/a>and the\u00a0<a href=\"https:\/\/www.cancer.gov\/\" target=\"_blank\" rel=\"noopener noreferrer\" data-saferedirecturl=\"https:\/\/www.google.com\/url?q=https:\/\/www.cancer.gov\/&amp;source=gmail&amp;ust=1613628187106000&amp;usg=AFQjCNEw8QyH7LtyaDDtT6v6qdhgPmGO5g\">National Cancer Institute\u00a0<\/a>(NIA and NCI; part of the National Institutes of Health, USA) and the<a href=\"http:\/\/www.nhmrc.gov.au\/\" target=\"_blank\" rel=\"noopener noreferrer\" data-saferedirecturl=\"https:\/\/www.google.com\/url?q=http:\/\/www.nhmrc.gov.au\/&amp;source=gmail&amp;ust=1613628187106000&amp;usg=AFQjCNGBFwfCpAU1tUNmqWkh6Pzu9AJH9w\">\u00a0National Health and Medical Research Council of Australia<\/a>.<\/li>\n<\/ul>\n<p>Download the <a title=\"The ASPREE XT Protocol \" href=\"https:\/\/aspree.org\/wp-content\/uploads\/sites\/3\/2023\/07\/ASPREE-XT-Protocol-v7-Feb-2023.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">ASPREE-XT Study Protocol<\/a><\/p>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][et_pb_row_inner admin_label=&#8221;TAB CONTENT&#8221; module_class=&#8221;tab-content&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; max_width=&#8221;840px&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column_inner saved_specialty_column_type=&#8221;2_3&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.16&#8243; header_2_font=&#8221;|600|||||||&#8221; header_2_font_size=&#8221;32px&#8221; header_2_font_size_tablet=&#8221;28px&#8221; header_2_font_size_phone=&#8221;24px&#8221; header_2_font_size_last_edited=&#8221;on|desktop&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h2>ASPREE Clinical Trial Protocol<\/h2>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;Trial protocol&#8221; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; text_text_color=&#8221;#000000&#8243; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h3>Summary<\/h3>\n<p>&nbsp;<\/p>\n<ul>\n<li>ASPREE (ASPirin in Reducing Events in the Elderly) was a double-blind, randomised, placebo-controlled primary prevention trial to determine whether daily active treatment of 100 mg enteric-coated aspirin extended the duration of disability-free life in healthy older adults.<\/li>\n<li>It was comprised of 19,114 community dwelling participants: 2,411 participants from centers across the United States and 16,703 participants from across south eastern Australia.<\/li>\n<li>While Australian participants were mainly Caucasians aged 70 and above, approximately half of the United States participants were ethnic minorities aged 65 years and older.<\/li>\n<li>All participants were free of overt cardiovascular disease, dementia and were otherwise healthy and able to perform basic activities of daily living (ADLs) independently at enrollment into ASPREE.<\/li>\n<li>The primary objective was to determine whether 100 mg aspirin prolonged life free of dementia, or life free of significant, persistent physical disability in the healthy elderly.<\/li>\n<li>Secondary objectives related to the effects of low-dose aspirin on the key outcome areas of death, cancer, depression, clinically significant bleeding, dementia, heart failure, myocardial infarction, physical disability, stroke\/TIA.<\/li>\n<li>Additional measures to those included in the primary and secondary objectives were hemoglobin levels, urine albumin: creatinine ratios, cognitive and physical function, and hospitalizations.<\/li>\n<li>The study examined whether the potential benefits of low-dose aspirin outweighed the risks in this age group.<\/li>\n<li>Participants were eligible for the trial if they did not have a current clinical indication for or contraindication (i.e. allergy or increased risk of bleeding) to aspirin, did not have dementia, significant physical disability, low hemoglobin levels, or have a condition that was likely to be fatal during the five years of the trial, and were capable of attending their usual Primary Care Providers (PCPs) clinic and providing informed consent.<\/li>\n<li>Sample size estimate required 19,000 participants to provide 90% power of a true relative risk benefit of 0.90 for the primary endpoint (a composite of all-cause mortality, incident dementia and persistent physical disability) in an intention-to-treat analysis with an average follow-up of 5 years.<\/li>\n<li>The trial received financial support from the\u00a0<a href=\"http:\/\/www.nia.nih.gov\/\" data-saferedirecturl=\"https:\/\/www.google.com\/url?q=http:\/\/www.nia.nih.gov\/&amp;source=gmail&amp;ust=1613628187106000&amp;usg=AFQjCNFjhAezSnFQ6YbXK0hf6WD2KTDziA\">National Institute on Aging\u00a0<\/a>and the\u00a0<a href=\"https:\/\/www.cancer.gov\/\" data-saferedirecturl=\"https:\/\/www.google.com\/url?q=https:\/\/www.cancer.gov\/&amp;source=gmail&amp;ust=1613628187106000&amp;usg=AFQjCNEw8QyH7LtyaDDtT6v6qdhgPmGO5g\">National Cancer Institute\u00a0<\/a>(NIA and NCI; part of the National Institutes of Health, USA), the\u00a0<a title=\"NHMRC website\" href=\"http:\/\/www.nhmrc.gov.au\/\" target=\"_blank\" rel=\"noopener noreferrer\" data-saferedirecturl=\"https:\/\/www.google.com\/url?q=http:\/\/www.nhmrc.gov.au\/&amp;source=gmail&amp;ust=1613628187106000&amp;usg=AFQjCNGBFwfCpAU1tUNmqWkh6Pzu9AJH9w\">National Health and Medical Research Council of Australia<\/a>,\u00a0<a href=\"https:\/\/www.monash.edu\/\">Monash University<\/a>\u00a0and the\u00a0<a title=\"VCA website\" href=\"http:\/\/www.victoriancanceragency.org.au\/\" target=\"_blank\" rel=\"noopener noreferrer\" data-saferedirecturl=\"https:\/\/www.google.com\/url?q=http:\/\/www.victoriancanceragency.org.au\/&amp;source=gmail&amp;ust=1613628187106000&amp;usg=AFQjCNHEssIJusC3vfFHs-t5fVbXxtNxeg\">Victorian Cancer Agency<\/a>.<\/li>\n<li>Bayer Pharma (Germany) provided in-kind support through the provision of low-dose aspirin and matching placebo and had no other involvement in the trial.<\/li>\n<li>ASPREE was conducted in community settings.<\/li>\n<\/ul>\n<p>Download the\u00a0<a title=\"The ASPREE Protocol \" href=\"\/wp-content\/uploads\/sites\/3\/2021\/07\/ASPREE-Protocol-Version-9_-Nov2014_FINAL-1.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">ASPREE Clinical Trial Protocol<\/a><\/p>\n<p>[\/et_pb_text][\/et_pb_column_inner][\/et_pb_row_inner][\/et_pb_column][\/et_pb_section][et_pb_section fb_built=&#8221;1&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; min_height=&#8221;100px&#8221; height=&#8221;100px&#8221; max_height=&#8221;100px&#8221; custom_margin=&#8221;-1px||-1px||false|false&#8221; custom_padding=&#8221;0px||0px||false|false&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_row column_structure=&#8221;1_2,1_2&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;1_2&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.20.4&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<p>Page updated:\u00a0 July 31, 2023<\/p>\n<p>[\/et_pb_text][\/et_pb_column][et_pb_column type=&#8221;1_2&#8243; _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;default&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=&#8221;1&#8243; _builder_version=&#8221;4.16&#8243; custom_padding=&#8221;90px||70px||false|false&#8221; border_width_top=&#8221;1px&#8221; border_color_top=&#8221;#cecece&#8221; saved_tabs=&#8221;all&#8221; locked=&#8221;off&#8221; global_colors_info=&#8221;{}&#8221;][et_pb_row use_custom_gutter=&#8221;on&#8221; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_column type=&#8221;4_4&#8243; _builder_version=&#8221;4.16&#8243; global_colors_info=&#8221;{}&#8221;][et_pb_text _builder_version=&#8221;4.16&#8243; _module_preset=&#8221;d100a70a-4a1b-4c0a-852d-deb7ebdb8d36&#8243; header_font=&#8221;|600||on|||||&#8221; header_text_align=&#8221;left&#8221; header_2_font=&#8221;|600||on|||||&#8221; header_2_text_align=&#8221;left&#8221; header_2_font_size=&#8221;32px&#8221; text_orientation=&#8221;center&#8221; custom_margin=&#8221;||0px||false|false&#8221; header_2_font_size_tablet=&#8221;28px&#8221; header_2_font_size_phone=&#8221;24px&#8221; header_2_font_size_last_edited=&#8221;on|desktop&#8221; global_colors_info=&#8221;{}&#8221;]<\/p>\n<h2>NEWS FOR CLINICIANS<\/h2>\n<p>[\/et_pb_text][et_pb_blog fullwidth=&#8221;off&#8221; posts_number=&#8221;3&#8243; include_categories=&#8221;13,15,16&#8243; show_author=&#8221;off&#8221; show_date=&#8221;off&#8221; show_categories=&#8221;off&#8221; masonry_tile_background_color=&#8221;rgba(0,0,0,0)&#8221; _builder_version=&#8221;4.20.4&#8243; header_level=&#8221;h4&#8243; header_font=&#8221;|600|||||||&#8221; header_font_size=&#8221;22px&#8221; custom_margin=&#8221;||40px||false|false&#8221; header_font_size_tablet=&#8221;20px&#8221; header_font_size_phone=&#8221;18px&#8221; header_font_size_last_edited=&#8221;on|desktop&#8221; border_width_all=&#8221;0px&#8221; global_colors_info=&#8221;{}&#8221;][\/et_pb_blog][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>\n","protected":false},"excerpt":{"rendered":"<p>FOR CLINICIANSThe ASPirin in Reducing Events in the Elderly (ASPREE) study continues to explore new ways to improve health and quality of life amongst older adults. The results will be relevant to many aging people around the world.The ASPREE Project &nbsp; \u00a0 \u2192\u00a0The ASPREE Clinical Trial (completed)\u00a0 \u2192 Major ASPREE trial findings \u2192\u00a0The ASPREE-XT (eXTension) [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":""},"_links":{"self":[{"href":"https:\/\/aspree.org\/usa\/wp-json\/wp\/v2\/pages\/102"}],"collection":[{"href":"https:\/\/aspree.org\/usa\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/aspree.org\/usa\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/aspree.org\/usa\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/aspree.org\/usa\/wp-json\/wp\/v2\/comments?post=102"}],"version-history":[{"count":55,"href":"https:\/\/aspree.org\/usa\/wp-json\/wp\/v2\/pages\/102\/revisions"}],"predecessor-version":[{"id":2787,"href":"https:\/\/aspree.org\/usa\/wp-json\/wp\/v2\/pages\/102\/revisions\/2787"}],"wp:attachment":[{"href":"https:\/\/aspree.org\/usa\/wp-json\/wp\/v2\/media?parent=102"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}