A Clinical Trial of Cognitive Behavior Therapy for Depression, Stigmatization, Excessive Worries, and Emotional Management Among Women Facing Partner Violence

NCT ID: NCT06208111

Last Updated: 2024-01-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

180 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-11-15

Study Completion Date

2024-04-10

Brief Summary

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1. Aim to investigate the effectiveness of Cognitive Behavior Therapy for Depression, Stigmatization, Excessive Worries, and Emotional Management among Women Facing Partner Violence
2. To explore the effectiveness of CBT in managing depressive symptoms, stigma, worries, and emotional disturbance among women facing partner violence.

Detailed Description

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In this Randomized control trial, N=180 participants would be enrolled for eligibility assessment from different shelter homes in the cities of Punjab after the eligibility assessment and screening 108 participants would be allocated to experimental and waitlist treatment conditions. Participants will be allocated through matchable group characteristics. Participant's age range would be between 18 to 45 years. Each of the group will be comprised of the same number of participants. Both groups will be pre-tested and results will be recorded. A cognitive behavior therapy-based treatment plan will be formulated to address Depression, Stigmatization, Excessive Worries, and Emotional Management among Women Facing Partner Violence. 8-10 CBT-based therapeutic sessions with 60 minutes will be conducted with the participant in a one-on-one setting.

Conditions

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Cognitive Behaviour Therapy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

A randomized control trial design will be used in this study. it would be two arm study and there would be two groups an experimental and a waitlist control group. The experimental group will receive intervention and another group will be placed on the waitlist. in this research parallel group design would be used. we will give treatment to all participants in a parallel way. The allocation ratio and framework would be equivalency i.e, the treatment group and control group be equal number of participants
Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Treatment group

Experimental Group:

participants in the experimental group would receive 8-10 Cognitive Behaviour Therapy-based therapeutic sessions.

Group Type EXPERIMENTAL

cognitive behavioral therapy

Intervention Type BEHAVIORAL

cognitive behavioral therapy would be used as intervention strategy for women facing partner violence to Clear about actual problems, re-educate about the issue of domestic problems and mental health, Logical expectations, Identify negative automatic thoughts,Thinking errors, and Improve understanding to identify which stressors trigger negative emotions. Moreover, this intervention will help to Prepare women how to deal with stress and overcome the reaction.

control group

Participants in the control group did not receive the said Cognative Behaviour Therapy intervention

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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cognitive behavioral therapy

cognitive behavioral therapy would be used as intervention strategy for women facing partner violence to Clear about actual problems, re-educate about the issue of domestic problems and mental health, Logical expectations, Identify negative automatic thoughts,Thinking errors, and Improve understanding to identify which stressors trigger negative emotions. Moreover, this intervention will help to Prepare women how to deal with stress and overcome the reaction.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Women living in the institutions for at least 2 weeks because of partner violence
* Second eligibility criteria would be women with a minimum of 1 year of marital relationship will be included.
* The age range would be 18 -48 years.
* Women whose scores are above average on the partner violence scale would be included in the study

Exclusion Criteria

* Women greater than 48 years and less than 18 years will be excluded.
* Women with medical and psychiatric comorbidities will be excluded.
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Government College University Faisalabad

OTHER

Sponsor Role lead

Responsible Party

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Qasir Abbas

Dr.Qasir Abbas Assistant Professor Clinical Psychology

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Qasir Abbas, PHD

Role: PRINCIPAL_INVESTIGATOR

Government College University Faisalabad

Locations

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Qasir Abbas

Faisalābad, Punjab Province, Pakistan

Site Status

Countries

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Pakistan

Other Identifiers

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GovernmentGUF

Identifier Type: -

Identifier Source: org_study_id

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