EQUIC-CC: Enhancing Quality of Informed Consent - Customized Consent

NCT00032539 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 240

Last updated 2012-03-16

No results posted yet for this study

Summary

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

Conditions

  • Healthy

Sponsors & Collaborators

Principal Investigators

  • Philip Lavori, PhD · Stanford University

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
1999-04-30
Primary Completion
1999-04-30
Completion
1999-04-30

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 NCT00032539 on ClinicalTrials.gov