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Completed No phase listed Observational Accepts healthy volunteers

Enhancing Quality of Informed Consent (EQUIC-DP) Developmental Phase

ClinicalTrials.gov ID: NCT00032552

Public ClinicalTrials.gov record NCT00032552. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 12:09 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

CSP #476DP - Enhancing Quality of Informed Consent (EQUIC-DP) Developmental Phase

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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

Study identification

NCT ID
NCT00032552
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Enrollment
632 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
Not listed
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 1999 (Type not available)
Primary completion
Feb 2006 (Actual)
Completion
Feb 2006 (Actual)
Last update posted
Mar 25, 2010

1999 – 2006

United States locations

U.S. sites
18
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
VA Medical Center, Birmingham Birmingham Alabama 35233 —
VA Palo Alto Health Care System Palo Alto California 94304-1207 —
MIMA Century Research Assoc. (CSP #424) (DP) Melbourne Florida 32901 —
West Palm Beach VA Medical Center West Palm Beach Florida 33410 —
Edward Hines, Jr. VA Hospital Hines Illinois 60141-5000 —
Richard Roudebush VA Medical Center, Indianapolis Indianapolis Indiana 46202-2884 —
VA Ann Arbor Healthcare System Ann Arbor Michigan 48113 —
VA Medical Center, Minneapolis Minneapolis Minnesota 55417 —
Mayo Clinic Rochester (CSP #424) (DP) Rochester Minnesota 55905 —
VA Medical Center, St Louis St Louis Missouri 63106 —
VA Sierra Nevada Health Care System Reno Nevada 89502 —
VA Western New York Healthcare System at Buffalo Buffalo New York 14215 —
New York Harbor HCS New York New York 10010 —
VA Medical Center, Northport Northport New York 11768 —
VA Medical Center, Durham Durham North Carolina 27705 —
VA Medical Center, Philadelphia Philadelphia Pennsylvania 19104 —
Michael E. DeBakey VA Medical Center (152) Houston Texas 77030 —
VA Puget Sound Health Care System, Seattle Seattle Washington 98108 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00032552, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 25, 2010 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00032552 live on ClinicalTrials.gov.

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