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Clinical and Cost-effectiveness of an Integrated Psychosocial Care Plan for Comorbid Depression in Breast Cancer Survivors In Pakistan: A Sequential Multiple Assignment Randomised Trial

Status: Recruiting
Location: See location...
Intervention Type: Other, Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Breast cancer is the most common cancer among women worldwide, and many survivors experience comorbid mental health conditions such as depression and anxiety, which can significantly worsen health outcomes and increase mortality. This large-scale trial in Pakistan aims to evaluate the clinical and cost-effectiveness of a three-stage adaptive intervention to manage depression among breast cancer survivors. Using a Sequential, Multiple Assignment, Randomised Trial (SMART) design, the study will recruit 26,372 participants aged 18 and above who have completed initial breast cancer treatment (surgery and/or chemotherapy or radiotherapy). Participants will be identified through primary care units, outpatient departments, oncology clinics in public hospitals, and charitable organisations across Pakistan. Depression will be screened using the Patient Health Questionnaire PHQ-9, with diagnosis confirmed by the Structured Clinical Interview Schedule of DSM (SCID). Those randomised to the intervention arm will receive adaptive interventions: starting with low-intensity guided self-help, followed by a high-intensity cognitive behavioural therapy-based programme called Moving On After Breast Cancer Plus (Moving on ABC Plus), and for non-responders, an additional pharmacological component will be introduced. Participants in both adaptive intervention and enhance usual care groups will be assessed at multiple time points-baseline, 6, 18, 30, and 48 weeks post-randomisation-using validated tools to measure depression (primary outcome), and anxiety, self-esteem, intrusive thoughts, health-related quality of life, satisfaction with services, and health resource use (secondary outcomes). The study will also include qualitative interviews and focus groups discussions with patients, caregivers, healthcare providers, and policymakers to identify barriers and facilitators to implementation and ensure the intervention is both contextually appropriate and scalable.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Women

• Aged 18 years and above

• Diagnosed with breast cancer (any stage)

• Completed initial treatment (i.e., surgery and/or radiotherapy or chemotherapy) for breast cancer (even if they are currently on hormonal therapy post-initial treatment)

• Total score of 10 or above on the Patient Health Questionnaire (PHQ-9)

• Diagnosis of current Major Depressive Episode (MDE) confirmed using the Structured Clinical Interview for DSM-5 (SCID).

Locations
Other Locations
Pakistan
Pakistan Institute of Living and Learning
RECRUITING
Karachi
Contact Information
Primary
Tayyeba Kiran, PhD
tayyaba.kiran@pill.org.pk
0923328262142
Backup
Nasim Chaudhry, MD
nasim.chaudhry@pill.org.pk
0922135371084
Time Frame
Start Date: 2025-06-13
Estimated Completion Date: 2028-12-30
Participants
Target number of participants: 26376
Treatments
Experimental: Adaptive interventions
The adaptive interventions include:~1. Non-specialist delivered Low intensity guided self-help (Khushi and Khatoon)~2. Moving on After Breast cancer Plus (Moving on ABC Plus)~3. Standard pharmacological intervention
Other: Enhanced Treatment As Usual (E-TAU)
Participants in this arm will continue to follow their routine visits to healthcare facilities. They will be regularly monitored by trained research team and will be assessed at weeks 6,18,30, and 48. In addition to psychological assessment at each follow-up, this will include information leaflets based on a brief psychoeducational module to educate participants about the risks, symptoms, management, and referral support information for anxiety and depression.
Related Therapeutic Areas
Sponsors
Leads: Pakistan Institute of Living and Learning
Collaborators: University of Sheffield, University of Manchester

This content was sourced from clinicaltrials.gov

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