CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 252 enrolled
Drug / intervention
Enhanced Consent Procedure +1 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00453544
NCT00453544N/ACompleted
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Enhancing Consent for Alzheimer's Research

University of California, San Diego·interventional·Posted Mar 29, 2007·Updated Jun 6, 2023

In Brief

A clinical study evaluating Enhanced Consent Procedure and Routine Consent Procedure for Alzheimer Disease. Completed, enrolled 252 participants across 1 site.

Detailed Summary

The purpose of this study is to evaluate the efficacy of an enhanced consent procedure for patients with mild-to-moderate Alzheimer disease, and to identify factors and patient characteristics that predict the degree to which enhanced consent is more beneficial than routine consent procedures.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAlzheimer Disease
CountriesUnited States
CollaboratorsNational Institute on Aging (NIA)

Timeline

N/ACompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMar 29, 2007
Enrollment StartApr 1, 2006
Primary CompletionSep 1, 2012
TodayJul 2, 2026
Enrollment to primary: 6.4 yearsPosted 19.3 years ago

Interventions

Enhanced Consent Procedureother

This is a procedure involving use of multimedia materials, as well as standard review with research staff, to see if the research consent procedure can be improved

Routine Consent Procedureother

This is a procedure designed to be in accord with standard research consent practices (and lacks multimedia aids)