Effects of the Stress Management Program on Stress and Coping Styles in Emotionally Abused Women
Strengthening the Psyche: The Online Stress Management Program on Stress and Coping Styles in Emotionally Abused Young Women: A Randomized Controlled Trial
1 other identifier
interventional
52
1 country
1
Brief 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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
March 30, 2025
CompletedFirst Submitted
Initial submission to the registry
November 20, 2025
CompletedFirst Posted
Study publicly available on registry
December 1, 2025
CompletedDecember 1, 2025
October 1, 2025
8 months
November 20, 2025
November 20, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change from Baseline in Perceived Stress Levels at Emotionally Abused Women Receiving the Online Stress Management Program
The scale is based on a 5-point Likert format, with scores ranging from 0 to 56
From enrollment to to the end of treatment at 6 weeks, one-month post-intervention, and three months post-intervention
Secondary Outcomes (1)
Change from Baseline in Perceived Stress Levels at Emotionally Abused Women Receiving the Online Stress Management Program.
From enrollment to the end of treatment at 6 weeks, one-month post-intervention, and three months post-intervention.
Study Arms (2)
experimental group
EXPERIMENTALThe intervention group received a six-week Online Stress Management Program delivered via Zoom, consisting of weekly sessions lasting 40-50 minutes each.
control group
NO INTERVENTIONNo intervention was applied to 26 participants
Interventions
The Online 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.
Eligibility Criteria
You may qualify if:
- being female
- over 18 years of age
- scoring above the mean on the Emotional Abuse Perceived Scale
- being a student at the university where the study was conducted
- having internet access
- not having any physical or mental health condition that could prevent participation
You may not qualify if:
- being male
- not over 18 years of age
- scoring lower the mean on the Emotional Abuse Perceived Scale
- having any physical or mental health condition that could prevent participation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Manisa Celal Bayar University
Manisa, 45010, Turkey (Türkiye)
Study Officials
- PRINCIPAL INVESTIGATOR
Nihan Durgu
Manisa Celal Bayar University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
November 20, 2025
First Posted
December 1, 2025
Study Start
February 1, 2024
Primary Completion
October 1, 2024
Study Completion
March 30, 2025
Last Updated
December 1, 2025
Record last verified: 2025-10
Data Sharing
- IPD Sharing
- Will not share
IPD will not be shared because of ethical considerations, privacy protection, and the sensitive nature of the data collected