Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
Healthy Volunteers
ID06687278

Effect of Interpersonal Relationship Psychotherapy-Based Intervention Program on Psychosocial Well-Being of Female Victims of Intimate Partner Violence

Led by Istanbul University - Cerrahpasa · Updated on 2025-04-29

40

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate the effect of an Interpersonal Relationship Psychotherapy-Based Intervention Program on the psychosocial well-being of female victims of intimate partner violence. The study focuses on understanding whether this program can improve interpersonal problems and mental well-being in women affected by such violence, addressing a critical gap in treatment options for this population. Participants in the intervention group will receive eight weekly individual psychotherapy sessions lasting 45 to 60 minutes each, designed to enhance interpersonal relationships and coping skills. A control group will continue with any existing medical or supportive care without additional intervention. The program duration spans approximately 2.5 to 3 months. During the study, participants will complete a series of assessments including the Inventory of Interpersonal Problems Circumplex Scales and Warwick-Edinburgh Mental Well-Being Scale at multiple points: during the second session, at the end of the eighth session, and within four weeks after the final session. Additional evaluations include the Beck Depression Inventory and program evaluation forms. These measures help monitor changes in interpersonal and mental health status throughout the study period.

CONDITIONS

Brief Title

Effectiveness of Interpersonal Relationship Psychotherapy Intervention for Female Victims of Intimate Partner Violence

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Proficiency in the Turkish language, including the ability to speak and understand it.
  • Exposure to any form of violence perpetrated by an intimate partner.
  • Female gender.
  • Age 18 years or older.
Not Eligible

You will not qualify if you...

  • Exposure to violence by an individual other than an intimate partner.
  • Presence of sensory loss, including hearing or vision impairments.
  • Physical injury or disability from violence that prevents participation.
  • Diagnosis of schizophrenia spectrum or other psychotic disorders.
  • Active self-destructive thoughts or plans.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - 2.5 to 3 months

Participants receive an Interpersonal Relationship Psychotherapy-Based Intervention Program consisting of eight individual weekly sessions, each lasting approximately 45-60 minutes, designed to improve psychosocial well-being.

8 weekly individual sessions

Follow-up

Duration - Up to 4 weeks

Participants are assessed within the four weeks following the final intervention session to evaluate lasting effects on psychosocial well-being.

1 to 2 visits

Trial Site Locations

Total: 1 location

1

Florence Nightingale Faculty of Nursing

Istanbul, Turkey (Türkiye), 34381

Actively Recruiting

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Research Team

C

Cennet Kara Özçalık

A

Asst. Prof.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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Published Research Related To This Trial

Risk Factors for Domestic Violence in Women and Predictors of Development of Mental Disorders in These Women.

Behice Han Almiş, Emel Koyuncu Kütük, Funda Gümüştaş...

https://pubmed.ncbi.nlm.nih.gov/30042644