Skip to content

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

Efficacy of CBT for Adherence and Depression in HIV Care Settings

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00951028
Enrollment
240
Registered
2009-08-04
Start date
2008-09-30
Completion date
2013-04-30
Last updated
2013-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression, HIV, HIV Infections

Keywords

Adherence

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).

Interventions

BEHAVIORALCognitive behavioral therapy (CBT) for adherence and depression (CBT-AD)

12 therapy sessions delivered over 4 months, using cognitive behavioral strategies to target depressive symptoms and adherence to HIV medications

BEHAVIORALLife-steps adherence treatment

Single-session adherence treatment that targets informational, problem solving, and cognitive-behavioral steps geared toward improving HIV medication adherence and self-management

BEHAVIORALInformation and supportive psychotherapy (ISP) for adherence and depression (ISP-AD)

12 therapy sessions delivered over 4 months, providing education and support that target depressive symptoms and adherence to HIV medications.

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Massachusetts General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
changes in HIV medication adherence, as measured by electronic medication event monitoring system (MEMS) pill-cap scoresMeasured at each visit - baseline, interim visits, and after 4, 8, and 12 monthsHIV medication adherence is assessed more frequently during the acute study period (baseline to post-treatment), and then at the follow up major visits.

Secondary

MeasureTime frameDescription
changes in Severity of depression, as assessed on the Montgomery-Asberg Depression Rating Scale (MADRS) by a blinded independent assessorMeasured at baseline and after 4, 8, and 12 months
changes in depression, as measured by the blinded assessor CGI ratingMeasured at baseline and after 4, 8, and 12 months
changes in RNA viral loadMeasured at baseline and after 4, 8, and 12 months
changes in CD4 cell countMeasured at baseline and after 4, 8, and 12 months
changes in self-reported depression (CESD)Measured at each visitThis is measured more frequently during the acute phase (pretreatment to post-treatment) then at the follow up assessments.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026