Effectiveness of Depression and Substance Use Module for Patients With Co-occurring Disorders (D-SUD-M)
15. juli 2026 oppdatert av: Somia Shabbir, International Islamic University, Islamabad
Adaptation And Effectiveness Of Depression And Substance Use Module For Patients With Substance Use Disorders And Depression in Pakistan
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.
Studieoversikt
Status
Aktiv, ikke rekrutterende
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
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:
- 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.
- 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.
- 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.
Studietype
Intervensjonell
Registrering (Faktiske)
50
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
-
Punjab Province
-
Rawalpindi, Punjab Province, Pakistan
- Najjat Trust
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Barn
- Voksen
Tar imot friske frivillige
Nei
Beskrivelse
Inclusion Criteria:
- Participants identified by the rehabilitation centre
- Only male participants will be taken,
- Age range lies between 17 to 56 years,
- Screening of depression by using the Beck Depression Inventory (BDI-II) and for Substance Use Disorders using Drug Abuse Screening Test (DAST-10),
- Diagnosed patients based on DSM-5 clinical diagnostic criteria will be taken into study.
Exclusion Criteria:
- Diagnosed cases of other psychopathology including bipolar disorder, psychotic depression, and others will not be taken in study,
- Cases of cognitive impairment linked to physical illness will not be part of the study.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Experimental Group: Treatment Module D-SUD-M
Participants in this group will recieve special treatment module D-SUD-M for patients with Depression and Substance Abuse.
|
A specialized psychological Intervention based module design for reducing the symptoms and to check the effectiveness of module on patients with depression and substance use disorder.
This module is translated and culturally adapted.
A manual treatment booklet was written in which eclectic approaches were used like Behaviour therapy, Cognitive behaviour therapy, relapse prevention, group therapy along with activity sheets for each session.
12 intervention based sessions will be given to the participants of this group.
No module based treatment will be given to the participants of this group.
|
|
Aktiv komparator: Control Group
No exposure of special treatment module will be given to the participants of this group.
|
No module based treatment will be given to the participants of this group.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in symptoms severity of depression from baseline to post-intervention
Tidsramme: Baseline to Post-intervention (5months) total weeks(22)
|
Assessed using the Beck Depression Inventory (BDI-II).
The BDI-II is a 21-item self-report scale measuring characteristics and symptoms of depression.
Total scores range from 0 to 63, with higher scores indicating a worse outcome (greater depressive symptom severity).
|
Baseline to Post-intervention (5months) total weeks(22)
|
|
Change in Substance Use Disorder Severity from baseline to post-intervention
Tidsramme: baseline to post-intervention (5months), total weeks (22)
|
Assessed using the Drug Abuse Screening Test (DAST-10).
The DAST -10 is a self-report instrument used to evaluate consequences related to drug misuse.
Total scores range from 0 to 10, with higher scores indicating a worse outcome (greater severity of substance use-related problems).
|
baseline to post-intervention (5months), total weeks (22)
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Studierekorddatoer
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Studer hoveddatoer
Studiestart (Faktiske)
2. mai 2026
Primær fullføring (Antatt)
30. september 2026
Studiet fullført (Antatt)
30. september 2026
Datoer for studieregistrering
Først innsendt
10. juli 2026
Først innsendt som oppfylte QC-kriteriene
10. juli 2026
Først lagt ut (Faktiske)
15. juli 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
16. juli 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
15. juli 2026
Sist bekreftet
1. juli 2026
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- IIUI/ORIC/Bioethics/110-
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