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| Sponsor: | National Institute of Mental Health (NIMH) |
|---|---|
| Information provided by: | National Institute of Mental Health (NIMH) |
| ClinicalTrials.gov Identifier: | NCT00602758 |
Purpose
This study will compare the effectiveness of enhanced counseling alone versus enhanced counseling combined with observed therapy at improving medication adherence in people with HIV.
| Condition | Intervention |
|---|---|
|
HIV Infections Acquired Immunodeficiency Syndrome |
Behavioral: Motivational interviewing with cognitive behavioral therapy Behavioral: Modified directly observed therapy |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study |
| Official Title: | ART Adherence: Enhanced Counseling and Observed Therapy |
| Enrollment: | 252 |
| Study Start Date: | December 2004 |
| Estimated Study Completion Date: | December 2009 |
| Estimated Primary Completion Date: | December 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Enhanced Counseling: Experimental
Participants meet with a counselor trained in motivational interviewing and cognitive behavioral techniques
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Behavioral: Motivational interviewing with cognitive behavioral therapy
Counseling sessions are completed face-to-face or by telephone at baseline and Weeks 1, 2, 4, 6, 9, 11, 15, 19, and 23. Counselors are trained in motivational interview technique and focus on ART medication adherence.
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Standard Care: No Intervention
Participants receive usual clinical care provided by health care providers and they participate only in evaluation components of the study
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Enhanced Counseling/Modified Directly Observed Therapy: Experimental
Participants receive their ART medications delivered to them by study staff and they receive the enhanced counseling
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Behavioral: Motivational interviewing with cognitive behavioral therapy
Counseling sessions are completed face-to-face or by telephone at baseline and Weeks 1, 2, 4, 6, 9, 11, 15, 19, and 23. Counselors are trained in motivational interview technique and focus on ART medication adherence.
Behavioral: Modified directly observed therapy
From baseline to Week 16, Monday through Friday, study staff meet the participants daily to observe one dose of their ART and to leave with the participants all other doses needed until the next observed dose. The frequency of observed doses begins to taper at Week 17 through to Week 24.
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HIV is a virus that can lead to acquired immunodeficiency syndrome (AIDS), a disease that breaks down the immune system and allows for entry of life-threatening secondary infections. HIV is transmitted through the exchange of bodily fluids, primarily through sexual intercourse. Antiretroviral therapy (ART) has proven to be an effective treatment for inhibiting the replication of HIV, allowing for improved quality of life and survival. However, the long-term effectiveness of ART depends on strict adherence to a prescribed medication regimen. Previous studies have indicated that observing patients while they take their medications for a period of time can improve adherence to their prescribed drug regimens. This study will evaluate the effectiveness of enhanced counseling (EC) alone versus EC combined with modified directly observed therapy (mDOT) at improving medication adherence in people with HIV.
Participants in this 48-week study will be randomly placed into one of the following three treatment groups:
All participants will continue to take the anti-HIV medication regimen prescribed by their health care provider. However, participants will be asked to keep one medication type in a bottle that has a special Micro-Electro-Mechanical System (MEMS) cap. This electronic cap will record each time the participant opens the bottle. Participants will meet with study staff for MEMS cap data collection once weekly for the first 4 weeks, every 2 weeks up to Week 12, and then every 4 weeks thereafter.
EC will consist of 30- to 45-minute counseling sessions about medication adherence. Participants will meet in person with a counselor for the first five sessions, occurring at baseline and Weeks, 1, 2, 6, and 11. An additional five counseling sessions will be conducted by phone during Weeks 4, 9, 15, 19, and 23. Participants receiving mDOT will have their doses of HIV medication delivered to them by an mDOT worker for the first 24 weeks of treatment. Participants will select a time and location to meet with an mDOT staff member, who will then provide the daily doses of drugs and observe participants taking those drugs. Participants will meet with an mDOT worker 5 times a week from baseline to Week 16. Starting at Week 17, the number of weekly meetings will gradually taper until Week 24 when there will be no meeting and participants will return to obtaining and taking their HIV medications as done prior to study enrollment.
Evaluation visits will occur for all participants at baseline and Weeks 12, 24, 36, and 48. Evaluation sessions will last 45 minutes to 1 hour and will include questionnaires about adherence, knowledge and attitudes about HIV and HIV therapy, quality of life, support systems, health status, medical history, drug and alcohol use, and satisfaction with HIV care. Blood samples will also be taken to measure CD4 cell count and amount of virus in the blood.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| United States, Kansas | |
| Kansas University Medical Center ID Clinic | |
| Kansas City, Kansas, United States, 66160 | |
| United States, Missouri | |
| Truman Medical Center ID Clinic | |
| Kansas City, Missouri, United States, 64108 | |
| Kansas City Free Health Clinic | |
| Kansas City, Missouri, United States, 64110 | |
| Kansas City Veterans Administration Medical Center | |
| Kansas City, Missouri, United States, 641128 | |
| Principal Investigator: | Kathy Goggin, PhD | University of Missouri, Kansas City |
More Information
| Responsible Party: | University of Missouri-Kansas City ( Kathleen Goggin, PhD ) |
| Study ID Numbers: | R01 MH068197, PA 01 0173, DAHBR 9A-ASGA |
| Study First Received: | January 4, 2008 |
| Last Updated: | October 27, 2008 |
| ClinicalTrials.gov Identifier: | NCT00602758 History of Changes |
| Health Authority: | United States: Federal Government |
|
AIDS Adherence Antiretroviral Therapy HIV |
|
RNA Virus Infections Sexually Transmitted Diseases, Viral Disease Slow Virus Diseases Immune System Diseases Acquired Immunodeficiency Syndrome Infection Immunologic Deficiency Syndromes |
Virus Diseases Pathologic Processes HIV Infections Syndrome Sexually Transmitted Diseases Lentivirus Infections Retroviridae Infections |