EQUIC-SM: Enhancing Quality of Informed Consent

NCT00032565 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 836

Last updated 2010-09-24

No results posted yet for this study

Summary

Patients in 'parent' cooperative studies projects are interviewed about their experiences in the informed consent process.

Conditions

  • Healthy
  • Informed Consent

Sponsors & Collaborators

Principal Investigators

  • Philip Lavori, PhD · VA Palo Alto Health Care System

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2002-11-30
Primary Completion
2007-07-31
Completion
2008-03-31

Countries

  • United States

Study Locations

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Entities

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 NCT00032565 on ClinicalTrials.gov