<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nuno MM</submitter><funding>NIA NIH HHS</funding><funding>National Institute on Aging</funding><pagination>81</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5628443</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Research has revealed that manifest Alzheimer's disease (AD) dementia is preceded by preclinical and prodromal phases during which pathology is accumulating but function remains intact. This understanding and concern that disease-modifying interventions initiated at the dementia stage may come too late in the neurodegenerative process to be successful has led to a paradigm shift in AD clinical trials. AD trials now enroll patients with mild cognitive impairment (MCI) and persons with no cognitive symptoms. Trial designs are similar to those enrolling dementia participants. We set out to test the hypothesis that attitudes towards trial design features differ among different potential AD trial populations.&lt;h4>Methods&lt;/h4>We sent a survey composed of 37 items assessing spec</pubmed_abstract><journal>Alzheimer's research &amp; therapy</journal><pubmed_title>Attitudes toward clinical trials across the Alzheimer's disease spectrum.</pubmed_title><pmcid>PMC5628443</pmcid><funding_grant_id>AG AG016573</funding_grant_id><funding_grant_id>AG016570</funding_grant_id><funding_grant_id>P50 AG016573</funding_grant_id><funding_grant_id>P50 AG016570</funding_grant_id><pubmed_authors>Dosanjh KK</pubmed_authors><pubmed_authors>Nuno MM</pubmed_authors><pubmed_authors>Brook J</pubmed_authors><pubmed_authors>Grill JD</pubmed_authors><pubmed_authors>Gillen DL</pubmed_authors><pubmed_authors>Elashoff D</pubmed_authors><pubmed_authors>Ringman JM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Attitudes toward clinical trials across the Alzheimer's disease spectrum.</name><description>&lt;h4>Background&lt;/h4>Research has revealed that manifest Alzheimer's disease (AD) dementia is preceded by preclinical and prodromal phases during which pathology is accumulating but function remains intact. This understanding and concern that disease-modifying interventions initiated at the dementia stage may come too late in the neurodegenerative process to be successful has led to a paradigm shift in AD clinical trials. AD trials now enroll patients with mild cognitive impairment (MCI) and persons with no cognitive symptoms. Trial designs are similar to those enrolling dementia participants. We set out to test the hypothesis that attitudes towards trial design features differ among different potential AD trial populations.&lt;h4>Methods&lt;/h4>We sent a survey composed of 37 items assessing spec</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Oct</publication><modification>2026-07-15T21:23:03.436Z</modification><creation>2026-07-09T10:13:39.215Z</creation></dates><accession>S-EPMC5628443</accession><cross_references><pubmed>28978335</pubmed><doi>10.1186/s13195-017-0311-5</doi></cross_references></HashMap>