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Therapy Targeting Depression and HIV Treatment Adherence (The TRIAD Study)

Primary Purpose

HIV, Depression, HIV Infections

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cognitive behavioral therapy (CBT) for adherence and depression (CBT-AD)
Life-steps adherence treatment
Information and supportive psychotherapy (ISP) for adherence and depression (ISP-AD)
Sponsored by
Massachusetts General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV focused on measuring Adherence

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • HIV-infected
  • Current diagnosis of depression or prescribed an antidepressant medication with at least some residual symptoms (e.g., clinical global impressions [CGI] scale score of 2 or greater)
  • Prescribed a stable regimen of highly active antiretroviral therapy (HAART) for HIV for at least 2 months

Exclusion Criteria:

  • Active, untreated, and unstable major mental illness (i.e., untreated psychosis or mania) that would interfere with cognitive behavioral therapy (CBT) treatment for depression
  • Diagnosis with any primary psychotic disorder, even if treated
  • Treatment with CBT within the past year

Sites / Locations

  • Massachusetts General Hospital
  • Fenway Community Health Center
  • Butler Hospital
  • The Miriam Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Active Comparator

Arm Label

Enhanced treatment as usual

CBT for adherence and depression (CBT-AD)

ISP for adherence and depression (ISP-AD)

Arm Description

Participants will receive the life-steps intervention and treatment as usual.

Participants will receive the life-steps and CBT-AD interventions.

Participants will receive the life-steps and ISP-AD interventions.

Outcomes

Primary Outcome Measures

changes in HIV medication adherence, as measured by electronic medication event monitoring system (MEMS) pill-cap scores
HIV medication adherence is assessed more frequently during the acute study period (baseline to post-treatment), and then at the follow up major visits.

Secondary Outcome Measures

changes in Severity of depression, as assessed on the Montgomery-Asberg Depression Rating Scale (MADRS) by a blinded independent assessor
changes in depression, as measured by the blinded assessor CGI rating
changes in RNA viral load
changes in CD4 cell count
changes in self-reported depression (CESD)
This is measured more frequently during the acute phase (pretreatment to post-treatment) then at the follow up assessments.

Full Information

First Posted
August 3, 2009
Last Updated
June 17, 2013
Sponsor
Massachusetts General Hospital
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT00951028
Brief Title
Therapy Targeting Depression and HIV Treatment Adherence (The TRIAD Study)
Official Title
Efficacy of CBT for Adherence and Depression in HIV Care Settings
Study Type
Interventional

2. Study Status

Record Verification Date
June 2013
Overall Recruitment Status
Completed
Study Start Date
September 2008 (undefined)
Primary Completion Date
April 2013 (Actual)
Study Completion Date
April 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will test a therapy for both helping people adhere to their HIV medication regimens and treating them for depression.
Detailed Description
People infected with HIV are more likely to suffer from depression than those not infected, with studies finding anywhere from 20% to 50% of HIV-infected individuals having significant depressive symptoms. Depression, in addition to causing persistent sadness and inability to feel pleasure, is related to a lack of HIV treatment adherence. Treatment adherence (making sure to take every pill as prescribed by doctors) is critically important to successful treatment of HIV, because missing even a few doses gives the HIV virus an opportunity to develop immunity to the medication. Poor adherence is related to worse medical outcomes, but even a small, 10% improvement rate in adherence may improve these outcomes. This study will test the efficacy of cognitive behavioral therapy (CBT) that addresses both depression and treatment adherence for HIV-infected people. Participation in this study will last 1 year, including follow-up visits. All participants will complete an initial one-visit intervention addressing treatment adherence. Then after 2 weeks, participants will be randomly assigned to one of three conditions: CBT for HIV medication adherence and depression (CBT-AD), information and supportive psychotherapy for HIV medication adherence and depression (ISP-AD), or enhanced treatment as usual (ETAU). Participants receiving CBT-AD and ISP-AD will complete 12 therapy sessions over 4 months and will be asked to report any changes to their psychological or HIV treatments. CBT-AD will involve learning to identify and change problematic patterns of thought and behavior, while ISP-AD will involve education and supportive psychotherapy. Participants receiving ETAU will receive only the initial session on HIV medication adherence and will be asked about their psychological and HIV treatment every other week for 4 months. Major study assessments will take place at baseline and after 4, 8, and 12 months. Assessments will include completing diagnostic interviews and questionnaires, measuring medication adherence through an electronic pill cap, and determining CD4 cell count and viral load (indicators of HIV treatment effectiveness).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV, Depression, HIV Infections
Keywords
Adherence

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
240 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Enhanced treatment as usual
Arm Type
Active Comparator
Arm Description
Participants will receive the life-steps intervention and treatment as usual.
Arm Title
CBT for adherence and depression (CBT-AD)
Arm Type
Experimental
Arm Description
Participants will receive the life-steps and CBT-AD interventions.
Arm Title
ISP for adherence and depression (ISP-AD)
Arm Type
Active Comparator
Arm Description
Participants will receive the life-steps and ISP-AD interventions.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive behavioral therapy (CBT) for adherence and depression (CBT-AD)
Intervention Description
12 therapy sessions delivered over 4 months, using cognitive behavioral strategies to target depressive symptoms and adherence to HIV medications
Intervention Type
Behavioral
Intervention Name(s)
Life-steps adherence treatment
Intervention Description
Single-session adherence treatment that targets informational, problem solving, and cognitive-behavioral steps geared toward improving HIV medication adherence and self-management
Intervention Type
Behavioral
Intervention Name(s)
Information and supportive psychotherapy (ISP) for adherence and depression (ISP-AD)
Intervention Description
12 therapy sessions delivered over 4 months, providing education and support that target depressive symptoms and adherence to HIV medications.
Primary Outcome Measure Information:
Title
changes in HIV medication adherence, as measured by electronic medication event monitoring system (MEMS) pill-cap scores
Description
HIV medication adherence is assessed more frequently during the acute study period (baseline to post-treatment), and then at the follow up major visits.
Time Frame
Measured at each visit - baseline, interim visits, and after 4, 8, and 12 months
Secondary Outcome Measure Information:
Title
changes in Severity of depression, as assessed on the Montgomery-Asberg Depression Rating Scale (MADRS) by a blinded independent assessor
Time Frame
Measured at baseline and after 4, 8, and 12 months
Title
changes in depression, as measured by the blinded assessor CGI rating
Time Frame
Measured at baseline and after 4, 8, and 12 months
Title
changes in RNA viral load
Time Frame
Measured at baseline and after 4, 8, and 12 months
Title
changes in CD4 cell count
Time Frame
Measured at baseline and after 4, 8, and 12 months
Title
changes in self-reported depression (CESD)
Description
This is measured more frequently during the acute phase (pretreatment to post-treatment) then at the follow up assessments.
Time Frame
Measured at each visit

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HIV-infected Current diagnosis of depression or prescribed an antidepressant medication with at least some residual symptoms (e.g., clinical global impressions [CGI] scale score of 2 or greater) Prescribed a stable regimen of highly active antiretroviral therapy (HAART) for HIV for at least 2 months Exclusion Criteria: Active, untreated, and unstable major mental illness (i.e., untreated psychosis or mania) that would interfere with cognitive behavioral therapy (CBT) treatment for depression Diagnosis with any primary psychotic disorder, even if treated Treatment with CBT within the past year
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven A. Safren, PhD
Organizational Affiliation
Partners HealthCare
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
C. Andres Bedoya, PhD
Organizational Affiliation
Partners HealthCare
Official's Role
Study Director
Facility Information:
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States
Facility Name
Fenway Community Health Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States
Facility Name
Butler Hospital
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02906
Country
United States
Facility Name
The Miriam Hospital
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02906
Country
United States

12. IPD Sharing Statement

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Therapy Targeting Depression and HIV Treatment Adherence (The TRIAD Study)

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