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Cognitive Behavior Therapy (CBT), Islamic Interventions (II) and Pharmacotherapy for Patients with Major Depressive Disorder-mild: A Randomized Control Trial

Cognitive Behavior Therapy (CBT), Islamic Interventions (II) and Pharmacotherapy for Patients with Major Depressive Disorder-mild: A Randomized Control Trial

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20201217004
Enrollment
Unknown
Registered
2020-12-17
Start date
2021-01-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Patients with mild severity would be included in the study. There is no harm and risk for the participants Cognitive Behavior Therapy Islamic iNterventions Major Depressive Disorder-Mild

Interventions

Cognitive Behavior Therapy base sessions would be conducted with the patients ,Islamic interventions would be planned and it would be designed according to the therapeutic goals. ,Waitlist group
Experimental Behavioral,Experimental Other,Placebo Comparator No treatment
CBT,Islamic Interventions,Waitlist

Sponsors

None
Lead Sponsor
None,None
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who will sign the consent will be included Only patients with mild severity will be included Patients having the ability to read, write and understand will be included

Exclusion criteria

Exclusion criteria: Patients with moderate to severe depressive disorder would be excluded Patients with physical and intellectual disability would be excluded Patients with the comorbid disorder would also be excluded Patients who will not complete the research procedure will be excluded

Design outcomes

Primary

MeasureTime frame
This study produced significant results. CBT and Islamic interventions produced substantial improvement in patients while psychotropic medication also produce better outcomes Study completed in four months period After initial screening patients were enrolled and interventions were given after it patients post test screening was conducted.

Secondary

MeasureTime frame
impacts of age, education, duration of illness and gender differences were investigated as secondary outcomes in the period of 4 months Clinical in depth interview was conducted with each patient and history of the problem and related demographic information were investigated

Countries

Pakistan

Contacts

Public ContactQasir Abbas

Government College University Faisalabad

qasirabbas47@yahoo.com923337683133

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026