Completed
A Study of Psychosocial and Behavioral Determinants of Differential Rates of Participant Compliance in CPCRA Protocols
Led by National Institute of Allergy and Infectious Diseases (NIAID) · Updated on 2013-10-01
557
Participants Needed
13
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
To examine, in patients enrolled in protocols CPCRA 006 and/or 007, the relationship between patient compliance and demographic, psychosocial, and lifestyle characteristics and Health Belief Model premises (i.e., patient's perception of susceptibility to and severity of disease and perception of benefits and barriers to a particular treatment) in order to design more effective intervention protocols. Patient noncompliance can influence the statistical findings of a clinical study, possibly resulting in an incorrect assessment of the effects of the investigational therapeutic agent. Since the special populations targeted by the CPCRA for inclusion in HIV-related clinical research do not typify those traditionally included in clinical trials or compliance research, it is necessary to elucidate and examine the special needs of these populations and to determine the extent to which these needs manifest themselves as potential barriers to protocol compliance.
CONDITIONS
Official Title
A Study of Psychosocial and Behavioral Determinants of Differential Rates of Participant Compliance in CPCRA Protocols
Who Can Participate
Eligibility Criteria
You may qualify if you...
Patients must meet the following criteria:
- New enrollment on CPCRA 006 or CPCRA 007.
- Life expectancy of at least 6 months.
- Willing and able, in clinician's opinion, to comply with treatment and clinical management.
- Able to read and write English or Spanish.
- Consent of parent of guardian for patients under 18 years.
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
Trial Site Locations
Total: 13 locations
1
Denver CPCRA / Denver Public Hlth
Denver, Colorado, United States, 80204
Status Unknown
2
Wilmington Hosp / Med Ctr of Delaware
Wilmington, Delaware, United States, 19899
Status Unknown
3
Veterans Administration Med Ctr / Regional AIDS Program
Washington D.C., District of Columbia, United States, 20422
Status Unknown
4
AIDS Research Consortium of Atlanta
Atlanta, Georgia, United States, 30308
Status Unknown
5
AIDS Research Alliance - Chicago
Chicago, Illinois, United States, 60657
Status Unknown
6
Louisiana Comm AIDS Rsch Prog / Tulane Univ Med
New Orleans, Louisiana, United States, 70112
Status Unknown
7
Comprehensive AIDS Alliance of Detroit
Detroit, Michigan, United States, 48201
Status Unknown
8
Henry Ford Hosp
Detroit, Michigan, United States, 48202
Status Unknown
9
North Jersey Community Research Initiative
Newark, New Jersey, United States, 07103
Status Unknown
10
Harlem AIDS Treatment Group / Harlem Hosp Ctr
New York, New York, United States, 10037
Status Unknown
11
Bronx Lebanon Hosp Ctr
The Bronx, New York, United States, 10456
Status Unknown
12
Portland Veterans Adm Med Ctr / Rsch & Education Grp
Portland, Oregon, United States, 97210
Status Unknown
13
Richmond AIDS Consortium
Richmond, Virginia, United States, 23298
Status Unknown
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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