NCT07258992

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
52

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2024

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2024

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 30, 2025

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

October 1, 2025

Completed
2 months until next milestone

First Posted

Study publicly available on registry

December 2, 2025

Completed
Last Updated

December 2, 2025

Status Verified

October 1, 2025

Enrollment Period

8 months

First QC Date

October 1, 2025

Last Update Submit

November 21, 2025

Conditions

Keywords

emotionally abusedwomenstressstress management programcoping stylesrandomized controlled tria

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

EXPERIMENTAL

The intervention group received a six-week Online Stress Management Program delivered via Zoom, consisting of weekly sessions lasting 40-50 minutes each.

Behavioral: Stress Management Program

control group

NO INTERVENTION

No intervention was applied to 26 participants

Interventions

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.

experimental group

Eligibility Criteria

Age18 Years+
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsEmotionally Abused Women
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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)

Amasya University

Amasya, 05100, Turkey (Türkiye)

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: 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.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

October 1, 2025

First Posted

December 2, 2025

Study Start

February 1, 2024

Primary Completion

October 1, 2024

Study Completion

March 30, 2025

Last Updated

December 2, 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

Locations