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Collaborative Care for the Detection and Management of Depression Among Adults Receiving Antiretroviral Therapy in South Africa

Collaborative Care for the Detection and Management of Depression Among Adults Receiving Antiretroviral Therapy in South Africa: a Pragmatic Cluster Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02407691
Acronym
COBALT
Enrollment
2002
Registered
2015-04-03
Start date
2015-04-30
Completion date
2018-01-31
Last updated
2023-11-29

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

Conditions

Chronic Diseases of Lifestyle, Depression, HIV/AIDS

Brief summary

With increasing access to antiretroviral therapy (ART) in South Africa, HIV has transitioned from a terminal illness to a long-term condition. It is likely to be accompanied by higher levels of disability and other chronic non-communicable diseases, resulting from the HIV itself, as well as adverse effects of medication. This requires an expansion of the purview of HIV care beyond direct HIV clinical care to also include a more comprehensive and integrated package of treatment and care for physical and mental conditions and their consequences. COBALT is a pragmatic cluster randomized controlled trial (RCT) in public sector primary care clinics in the North West Province of SA. It will assess mental health and HIV outcomes for depressed adults receiving ART by measuring the real-world effectiveness of a facility-based stepped care intervention combining depression case detection by non-physician clinicians with group counselling intervention delivered by lay-health workers.

Interventions

OTHERPrimary care 101 plus mental health

A facility-based stepped care intervention combining depression case detection by non-physician clinicians with group counselling intervention delivered by lay-health workers.

OTHERStandard Primary Care 101

Standard Primary Care 101 guideline with standard training

Sponsors

King's College London
CollaboratorOTHER
University of KwaZulu
CollaboratorOTHER
University of Cape Town
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

Clinics: 1\) 40 nurse-led primary care clinics providing ART in the Dr Kenneth Kaunda and Bojonala districts of the North West Province, South Africa Patients: 1. Age ≥ 18 years and 2. Receiving ART at the time of enrollment and 3. Depressive symptoms, as indicated by a total score of 9 or more on the PHQ-9 and 4. Planning to reside in the area for the next year and 5. Capable of actively engaging in an interviewer-administered questionnaire at the time of recruitment, six and twelve months later and 6. Written consent to participate in the study

Exclusion criteria

Clinics: 1\) Clinics which participate in the formative research and piloting of the intervention Patients: 1\) Inability to meet the above inclusion criteria

Design outcomes

Primary

MeasureTime frameDescription
Viral load suppression12 monthsviral load value of \<1000 RNA copies/ml
Patient Health Questionnaire 9 (PHQ-9) response6 monthsAt least 50% improvement in PHQ-9 score compared with baseline

Secondary

MeasureTime frameDescription
Depression Remission at 12 months12 monthsScore of less than 5 in PHQ-9
Mean PHQ-9 score at 6 and 12 months6 and 12 monthsAverage score in the PHQ-9
Antiretroviral therapy programme retention12 monthscontinuation in the ART programme
Viral load suppression at 12 months12 monthsDefined as a viral load of \<400 copies/ml
Virological failure12 monthsDefined as two viral load values \>1000 copies/ml
Appropriate maintenance on enrollment ART regimen OR ART regimen switched to second-line12 monthscontinuation with the ART regimen OR change
ART adherence12 months30 day VAS self reported measure
Change in viral load values over time12 monthschange in HIV RNA copies measured by PCR
Depression severity (categorised as mild, moderate, moderately severe or severe depression at 6 and 12 months)6 and 12 monthsMild depression defined as a score of 5 to 9; moderate depression defined as a score of 10-14 Moderately severe depression defines as a core of 15-19, and Severe depression defined as a score of 20-27.
PHQ-9 Response at 12 months12 monthsAt least 50% improvement in PHQ-9 score compared with baseline
Risk factors for cardiovascular diseases12 monthsMeasured by blood pressure, weight, smoking status
Detection and treatment of other chronic diseases12 monthsIdentification of new cases of NCDs or risk factors of Chronic deseases
Provision of integrated care from patient perspective12 monthsAssessed using the Patient Assessment of Care for Chronic Conditions (PACIC)
Antidepressant treatment initiated or intensified12 monthsstart or intensification of anti-depressants after baseline
Counselling for depression by a clinic-based counsellor12 monthsHaving counselling sessions with the clinic counsellor
Referral to specialist mental health worker/service12 monthsReferral by a nurse to mental health worker/service
Hospital admissions12 monthsnumber and duration of overnight hospital stays
Mortality12 monthsMortality reported at loss to follow-up or through the South African Population register
Stress12 monthsMeasured through the Percieved Stress Scale
Stigma12 monthsMeasured through the 6-item AIDS related stigma scale

Other

MeasureTime frameDescription
Disability12 monthsMeasured by WHODAS 2
Productivity and economic measures12 monthsSelf reported
Care utilization and resource use12 monthsMeasured by service use questionnaire

Countries

South Africa

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 11, 2026