Adaptation And Effectiveness Of Depression And Substance Use Module For Patients With Substance Use Disorders And Depression in Pakistan
| Registry | NCT07705113, acronym D-SUD-M |
|---|---|
| Status | Active not recruiting |
| Phase | Not applicable |
| Study type | Interventional; randomized, parallel, masking: single, treatment |
| Enrollment | 50 (Actual) |
| Sponsor | International Islamic University, Islamabad (Other) |
| Conditions | Depression, Substance Use Disorders |
| Interventions | Experimental Group: Treatment Module D-SUD-M, Control Group (Behavioral) |
| Dates | start 2026-05-02, primary completion 2026-09-30 (estimated), completion 2026-09-30 (estimated), first posted 2026-07-15, last updated 2026-07-16 |
| Locations | 1 site in Pakistan |
Related Papers Related Patents Related Grants Related Experts
All trials for Depression All trials for Substance Use Disorders All trials of Experimental Group: Treatment Module D-SUD-M All trials of Control Group
The purpose of this study is to evaluate the adaptation and effectiveness of an integrated treatment module, the Depression and Substance Use Disorder Module (D-SUD-M), for male patients experiencing co-occurring depression and substance use disorders in Pakistan.
Participants are divided into two groups: an experimental group receiving the structured D-SUD-M intervention-based sessions and a control group receiving standard routine treatment sessions within the rehabilitation center.
The primary objective is to evaluate whether the specialized intervention module significantly reduces depressive symptoms and substance use severity compared to routine standard care.
A total of 50 male participants aged 17 to 56 years admitted to a rehabilitation facility are enrolled in this parallel-group interventional study.
The research is structured as follows:
1. Pre-Assessment Screening: All participants are initially screened using the Beck Depression Inventory (BDI-II) to assess depression levels and the Drug Abuse Screening Test (DAST-10) to assess substance use severity.
2. Group Assignment: Participants are allocated to either the experimental group or the control group. The experimental group undergoes the designated treatment module (D-SUD-M) over a 12-session course spanning approximately 5 months (22 weeks). The control group undergoes routine rehabilitation facility program care without the specific D-SUD-M intervention.
3. Post-Assessment Screening: Following the completion of the intervention period at 22 weeks, both groups are re-evaluated using the exact same screening instruments (BDI-II and DAST-10) to statistically analyze symptom reduction and measure module effectiveness.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Experimental Group: Treatment Module D-SUD-M | Experimental | Behavioral: Experimental Group: Treatment Module D-SUD-M; Behavioral: Control Group | Participants in this group will recieve special treatment module D-SUD-M for patients with Depression and Substance Abuse. |
| Control Group | Active comparator | Behavioral: Control Group | No exposure of special treatment module will be given to the participants of this group. |
Sex: Male, ages: 17 Years to 56 Years
Inclusion Criteria: 1. Participants identified by the rehabilitation centre 2. Only male participants will be taken, 3. Age range lies between 17 to 56 years, 4. Screening of depression by using the Beck Depression Inventory (BDI-II) and for Substance Use Disorders using Drug Abuse Screening Test (DAST-10), 5. Diagnosed patients based on DSM-5 clinical diagnostic criteria will be taken into study. Exclusion Criteria: 1. Diagnosed cases of other psychopathology including bipolar disorder, psychotic depression, and others will not be taken in study, 2. Cases of cognitive impairment linked to physical illness will not be part of the study.
| Facility | City | Country | Status |
|---|---|---|---|
| Najjat Trust | Rawalpindi, Punjab Province | Pakistan |