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Behavioural Activation for Comorbid Depression in Non-communicable Disease (BEACON) study

Not Applicable
Completed
Conditions
Health Condition 1: E08-E13- Diabetes mellitusHealth Condition 2: I00-I99- Diseases of the circulatory systemHealth Condition 3: J00-J99- Diseases of the respiratory systemHealth Condition 4: F32- Major depressive disorder, singleepisode
Registration Number
CTRI/2020/05/025048
Lead Sponsor
Dr Arun Kandasamy
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
56
Inclusion Criteria

Aged 18 years or over

Diagnosed with cardiovascular disease, chronic respiratory disease or diabetes (type 1 or 2)

Current diagnosis of depression (confirmed with a clinician-administered PHQ-9 score of � 10)48

Willing to participate and able to attend therapy sessions in person or by telephone

Other mental or physical illness comorbidities will not be a reason to exclude unless the patient is judged to be too unwell to participate

Exclusion Criteria

Already receiving psychotherapy for depression. Being on antidepressant medication will not however be a reason to exclude.

Lacking capacity to provide informed consent

Unable to take part in therapy because of cognitive impairment, or severity of mental or physical illness

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
A refined BA intervention, BEACON, including intervention manual, workbooks and training package, ready for trial intervention <br/ ><br> <br/ ><br>An optimised protocol for evaluation of effectiveness and cost effectiveness of BEACON for depression in NCD in LMIC, including an intervention fidelity framework and protocols for process evaluationTimepoint: Baseline and 3 months <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
Anxiety (GAD-7) <br/ ><br>Health related quality of life (EQ-5D-5L) <br/ ><br>Physical health, using a measure of quality of life and function S(F-36) <br/ ><br>NCD specific outcomes (HbA1c; Blood Pressure, respiratory quality of life)Timepoint: Baseline and 3 months <br/ ><br>
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