Effectiveness of Coping Training for People With HIV Experiencing Treatment Side Effects (The Balance Project)
Primary Purpose
HIV Infections
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cognitive behavioral coping effectiveness training
Standard care
Single group workshop on coping effectiveness training
Sponsored by

About this trial
This is an interventional supportive care trial for HIV Infections focused on measuring Side Effects, Adherence, Coping, HIV, AIDS, Complementary Therapies
Eligibility Criteria
Inclusion Criteria:
- Confirmed presence of HIV infection
- Currently receiving ART
- Experiencing ART side effects
Exclusion Criteria:
- Currently enrolled in another trial
- Evidence of psychosis or cognitive impairment
Sites / Locations
- University of California, San Francisco
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
1
2
Arm Description
Participants will receive five individual sessions of coping effectiveness training.
Participants will receive standard care and one delayed group workshop of coping effectiveness training.
Outcomes
Primary Outcome Measures
Quality of life
Secondary Outcome Measures
Medication adherence
Full Information
NCT ID
NCT00643903
First Posted
March 24, 2008
Last Updated
January 18, 2012
Sponsor
University of California, San Francisco
Collaborators
National Institute of Mental Health (NIMH)
1. Study Identification
Unique Protocol Identification Number
NCT00643903
Brief Title
Effectiveness of Coping Training for People With HIV Experiencing Treatment Side Effects (The Balance Project)
Official Title
The Balance Project - RCT of an HIV Treatment Side Effects Coping Intervention
Study Type
Interventional
2. Study Status
Record Verification Date
January 2012
Overall Recruitment Status
Completed
Study Start Date
April 2004 (undefined)
Primary Completion Date
September 2008 (Actual)
Study Completion Date
February 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
National Institute of Mental Health (NIMH)
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study will evaluate the effectiveness of cognitive behavioral coping training in improving side effect management and treatment adherence in HIV-infected patients who are taking antiretroviral medications.
Detailed Description
HIV is a virus that is transmitted through the exchange of bodily fluids, primarily through sexual intercourse. HIV infections can lead to acquired immunodeficiency syndrome (AIDS), a disease that breaks down the immune system and allows for entry of life-threatening secondary infections. Antiretroviral therapy (ART) has proven to effectively inhibit the replication of HIV and has resulted in a reduction in HIV-related deaths. People infected with HIV who are receiving ART, however, may be confronted with negative physical and emotional side effects. These side effects can impact quality of life (QOL), adherence to medical care, and decisions about health care. Stress and Coping Theory (SCT) is a person-centered approach that considers stressful experiences as person-environment transactions. A cognitive behavioral treatment based upon SCT may help to eliminate or reduce the negative impact of side effects, improve QOL, and maximize benefit from treatment among people living with HIV. This study will evaluate the effectiveness of cognitive behavioral coping training in improving side effect management and treatment adherence in HIV-infected people who are taking ART medications.
This study will involve two phases. Phase 1 will be conducted over 12 months and will include two 1-hour interviews with questions about personal life, family, friends, medications, and medication side effects. After the first interview, participants may be invited to participate in Phase 2, which will last 18 months.
During Phase 2, participants will complete five 2- to 3-hour interviews occurring at baseline and Months 3, 6, 12, and 18. Interviews will include questions about personal life, friends, family, health-related activities, drug-using behaviors, emotions, mental state, and educational background. Participants will be assigned randomly to one of two treatment groups:
Group 1 participants will receive five individual sessions of cognitive behavioral coping training, beginning after the Month 3 interview. The 90-minute sessions will focus on coping with stress, dealing with medication side effects, and staying on track with medications.
Group 2 participants will receive standard care and one group session of coping training, which will be held after the Month 18 interview. The group session will cover the same material that is covered in the individual sessions.
After the last follow-up interview, some participants may also be asked to complete an exit interview about thoughts and feelings on study participation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Side Effects, Adherence, Coping, HIV, AIDS, Complementary Therapies
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
250 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Participants will receive five individual sessions of coping effectiveness training.
Arm Title
2
Arm Type
Active Comparator
Arm Description
Participants will receive standard care and one delayed group workshop of coping effectiveness training.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive behavioral coping effectiveness training
Intervention Description
Coping effectiveness training will include five individual 90-minute counseling sessions. The sessions will focus on coping with stress, dealing with medication side effects, and staying on track with medications.
Intervention Type
Behavioral
Intervention Name(s)
Standard care
Intervention Description
Participants will receive standard of care for HIV infections.
Intervention Type
Behavioral
Intervention Name(s)
Single group workshop on coping effectiveness training
Intervention Description
Participants will attend one group workshop covering the same material as in the individual sessions. The workshop will be delivered after completion of the Month 18 final assessment.
Primary Outcome Measure Information:
Title
Quality of life
Time Frame
Measured at Month 18
Secondary Outcome Measure Information:
Title
Medication adherence
Time Frame
Measured at Month 18
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Confirmed presence of HIV infection
Currently receiving ART
Experiencing ART side effects
Exclusion Criteria:
Currently enrolled in another trial
Evidence of psychosis or cognitive impairment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mallory O. Johnson, PhD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94105
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Effectiveness of Coping Training for People With HIV Experiencing Treatment Side Effects (The Balance Project)
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