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Effects of a Stress Management Program on Stress and Coping Styles in Emotionally Abused Women

NCT07258992 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2025-12-02

No results posted yet for this study

Summary

The goal of this clinical trial is to examine the effectiveness of a structured stress management intervention in promoting healthier coping mechanisms and reducing perceived stress levels among emotionally abused young women. The main questions it aims to answer are:

H1: Women who participate in the OSM program will show a significant reduction in perceived stress levels compared to the control group.

H2: Women who participate in the OSM program will show a significant improvement in coping style levels compared to the control group.

Researchers will compare a structured stress management program to usual conditions to see if it promotes healthier coping mechanisms and reduces perceived stress levels among emotionally abused young women.

Participants will:

Receive a 6-week Online Stress Management Program Attend six weekly sessions (40-50 minutes each) delivered via Zoom

Conditions

  • Abused Women

Interventions

BEHAVIORAL

Stress Management Program

The Stress Management Program was implemented with participants who met the eligibility criteria and completed the pretest. The program aimed to enhance participants' stress management and emotional regulation skills while fostering psychological empowerment. Conducted by a psychiatric nurse with a PhD, the program consisted of six weekly sessions (40-50 minutes each) delivered via Zoom.

Sponsors & Collaborators

  • Manisa Celal Bayar University

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-02-01
Primary Completion
2024-10-01
Completion
2025-03-30

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07258992 on ClinicalTrials.gov