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Comparison of Video Consent Versus Routine Consent for Participation in Research Studies

NCT00430391 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 382

Last updated 2013-06-19

No results posted yet for this study

Summary

The purpose of this study is to examine a novel technique for improving the informed consent process for participation in research by the older psychiatric population.

Conditions

Interventions

OTHER

DVD Consent

Participants are randomized to DVD enhanced consent that is either high risk or low risk.

OTHER

Routine Control

Participants are assigned to the routine, standard consent.

Sponsors & Collaborators

Principal Investigators

  • Dilip V. Jeste, MD · UCSD

Study Design

Allocation
RANDOMIZED
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2003-12-31
Primary Completion
2010-02-28
Completion
2010-02-28

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00430391 on ClinicalTrials.gov