Effectiveness of Enhanced Counseling and Observed Therapy on Antiretroviral Adherence in People With HIV
Primary Purpose
HIV Infections, Acquired Immunodeficiency Syndrome
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Motivational interviewing with cognitive behavioral therapy
Modified directly observed therapy
Sponsored by
About this trial
This is an interventional treatment trial for HIV Infections focused on measuring AIDS, Adherence, Antiretroviral Therapy, HIV
Eligibility Criteria
Inclusion Criteria:
- Patient at participating clinical site
- English-speaking
- Initiating new ART (new or change in therapy) or nonadherent to ART as documented by care provider's assessment, patient self-report, and consistent HIV RNA laboratory results
- Lives within 45-mile radius of participating clinical site or able to participate in observed therapy procedures
Exclusion Criteria:
- Pregnancy
Sites / Locations
- Kansas University Medical Center ID Clinic
- Truman Medical Center ID Clinic
- Kansas City Free Health Clinic
- Kansas City Veterans Administration Medical Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
No Intervention
Experimental
Arm Label
Enhanced Counseling
Standard Care
Enhanced Counseling/Modified Directly Observed Therapy
Arm Description
Participants meet with a counselor trained in motivational interviewing and cognitive behavioral techniques
Participants receive usual clinical care provided by health care providers and they participate only in evaluation components of the study
Participants receive their ART medications delivered to them by study staff and they receive the enhanced counseling
Outcomes
Primary Outcome Measures
Adherence with ART as measured by Micro-Electro-Mechanical Systems (MEMS)
Secondary Outcome Measures
HIV RNA suppression
Full Information
NCT ID
NCT00602758
First Posted
January 4, 2008
Last Updated
May 19, 2016
Sponsor
University of Missouri, Kansas City
Collaborators
National Institute of Mental Health (NIMH)
1. Study Identification
Unique Protocol Identification Number
NCT00602758
Brief Title
Effectiveness of Enhanced Counseling and Observed Therapy on Antiretroviral Adherence in People With HIV
Official Title
ART Adherence: Enhanced Counseling and Observed Therapy
Study Type
Interventional
2. Study Status
Record Verification Date
May 2016
Overall Recruitment Status
Completed
Study Start Date
December 2004 (undefined)
Primary Completion Date
August 2009 (Actual)
Study Completion Date
August 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Missouri, Kansas City
Collaborators
National Institute of Mental Health (NIMH)
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
Detailed Description
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:
Group 1 participants will receive standard care, which will involve the care that the clinic staff normally provide to all patients on HIV therapy.
Group 2 participants will receive EC.
Group 3 participants will receive EC with mDOT.
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections, Acquired Immunodeficiency Syndrome
Keywords
AIDS, Adherence, Antiretroviral Therapy, HIV
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
252 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Enhanced Counseling
Arm Type
Experimental
Arm Description
Participants meet with a counselor trained in motivational interviewing and cognitive behavioral techniques
Arm Title
Standard Care
Arm Type
No Intervention
Arm Description
Participants receive usual clinical care provided by health care providers and they participate only in evaluation components of the study
Arm Title
Enhanced Counseling/Modified Directly Observed Therapy
Arm Type
Experimental
Arm Description
Participants receive their ART medications delivered to them by study staff and they receive the enhanced counseling
Intervention Type
Behavioral
Intervention Name(s)
Motivational interviewing with cognitive behavioral therapy
Other Intervention Name(s)
Enhanced counseling (EC)
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Modified directly observed therapy
Other Intervention Name(s)
OT, Modified observed therapy (MDOT)
Intervention Description
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.
Primary Outcome Measure Information:
Title
Adherence with ART as measured by Micro-Electro-Mechanical Systems (MEMS)
Time Frame
Measured at Week 48
Secondary Outcome Measure Information:
Title
HIV RNA suppression
Time Frame
Measured at Week 48
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient at participating clinical site
English-speaking
Initiating new ART (new or change in therapy) or nonadherent to ART as documented by care provider's assessment, patient self-report, and consistent HIV RNA laboratory results
Lives within 45-mile radius of participating clinical site or able to participate in observed therapy procedures
Exclusion Criteria:
Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kathy Goggin, PhD
Organizational Affiliation
University of Missouri, Kansas City
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kansas University Medical Center ID Clinic
City
Kansas City
State/Province
Kansas
ZIP/Postal Code
66160
Country
United States
Facility Name
Truman Medical Center ID Clinic
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64108
Country
United States
Facility Name
Kansas City Free Health Clinic
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64110
Country
United States
Facility Name
Kansas City Veterans Administration Medical Center
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
641128
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
17639650
Citation
Goggin K, Liston RJ, Mitty JA. Modified directly observed therapy for antiretroviral therapy: a primer from the field. Public Health Rep. 2007 Jul-Aug;122(4):472-81. doi: 10.1177/003335490712200408.
Results Reference
background
Links:
URL
http://cas.umkc.edu/psyc/motiv8/
Description
Click here for more information on the Kansas City Adherence Study (MOTIV8)
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Effectiveness of Enhanced Counseling and Observed Therapy on Antiretroviral Adherence in People With HIV
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