Clinical Trials Logo

Clinical Trial Summary

This research was designed as a randomized controlled experimental study with pretest posttest and repeated measurement in order to examine the Effect of Solution-Focused Approach on Attitudes to Violence Against Women in High School Students. The research sample consisted of 90 students (45 control, 45 experiment) who met the inclusion criteria of the research out of 1037 students studying at 5 high schools randomly selected from the central high schools affiliated to the Muş Provincial Directorate of National Education. Personal Information Form and Violence Against Women Attitude Scale (İSKEBE) were used to collect data. The Personal Information Form was filled in by the students themselves before the program. İSKEBE was filled before, after the program and at the follow-up 3 months later. 3 days were determined for the program for the students in the experimental group, and the program was applied for 60 minutes a day for 6 weeks, allowing the students to participate in the program on a suitable day. No intervention was made to the control group during the program. Before the program, the personal characteristics of the control and experimental group students were similar in terms of İSKEBE and subscale scores.


Clinical Trial Description

Initiatives for the Experimental Group Personal Information Form and İSKEBE scale were given to 45 students who were determined in accordance with the research criteria and they were asked to fill in. Data were collected from students who did not come to school that day by telephone or by interviewing them the next day. Before the solution-oriented approach program, the students were interviewed and the appropriate time and hours were determined for the program. Then, an online solution-oriented approach program was implemented, which lasted for 6 weeks at the specified hours and days. In the first week of the program, a guide form containing the activities related to the program to be applied was distributed to the students. At the end of the program, the students were asked to fill in the İSKEBE scale as a post-test. Three months after the end of the program, they were asked to fill in the İSKEBE scale again as a follow-up test. Initiatives for the Control Group Personal Information Form and İSKEBE scale were given to 45 students who were determined in accordance with the research criteria and they were asked to fill in. Data were collected by phone calls or the next day with students who did not come to school that day. 6 weeks after the pre-test application, the students were asked to fill in the İSKEBE scale as a post-test. Three months after the post-test application, they were asked to fill out the İSKEBE scale again as a follow-up test. At the end of the follow-up test, 45 minutes of violence against women training was given to the control group students. During the conduct of the research, both control and experimental group students routinely attended their schools. In addition, no changes were made in the daily life routines of the students. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05417919
Study type Interventional
Source Mus Alparlan University
Contact
Status Completed
Phase N/A
Start date November 2, 2021
Completion date June 1, 2022

See also
  Status Clinical Trial Phase
Completed NCT06284148 - Confidential IPV Screening Tool N/A
Completed NCT04095429 - Expect Respect Middle School Randomized Trial N/A
Recruiting NCT06100679 - Responsible Engaged and Loving (REAL) Fathers Intervention Evaluation N/A
Recruiting NCT05331352 - Attachment Style and Mentalization Impact Among Women Victims of Domestic Violence N/A
Completed NCT04625465 - Proximal Effects of Alcohol on Same-Sex Intimate Partner Violence N/A
Not yet recruiting NCT06350383 - Adapting a Low-cost Intimate Partner Violence and Mental Health Response Intervention N/A
Completed NCT03259646 - The IPV Provider Network: Engaging the Health Care Provider Response to Interpersonal Violence Against Women N/A
Not yet recruiting NCT06330753 - Synergy Between Patient and Clinician: Using a Trauma-Informed Care Plan N/A
Not yet recruiting NCT05310656 - Evaluation of the Impact of the Empowerment Program on Sheltered Battered Women N/A
Recruiting NCT03623555 - Applied Social Neuroscience: the Building Resilience Among Women Project
Recruiting NCT05608421 - 1MoreStep: An Intervention to Increase HIV Care Engagement and Reduce Intimate Partner Violence Among Black Women Living With HIV N/A
Recruiting NCT05609786 - Dissemination and Implementation of a Web-based Relationship Safety App, myPlanKenya, for Women at Risk for Intimate Partner Violence in Nairobi, Kenya N/A
Recruiting NCT06001307 - Supporting Trans Affirmation, Relationships, and Sex, Phase 3 N/A
Not yet recruiting NCT05768217 - Community Resiliency Collective Efficacy Intervention N/A
Completed NCT04950686 - Study of Long-term Efficacy and Mechanisms Underlying the Impact of a Web-based Sexual and Relationship Health Promotion Program With Young Adult Community College Students N/A
Completed NCT03539315 - Adaptation and Testing of the Addressing Reproductive Coercion in HEalth Settings (ARCHES) Intervention in Bangladesh N/A
Recruiting NCT03498638 - Feasibility Study of Couple Therapy Treatment for Situational Couple Violence N/A
Recruiting NCT04098276 - It's WeWomen Plus Intervention for Health, Safety and Empowerment N/A
Completed NCT05163171 - Prevalence of the Victimization and the Perpetration of Intimate Partner Violence Among the Patients From Puy-de-Dôme and Paris Consulting or Being Hospitalized for Addiction Problems and Their Expectations From General Practitioners (VIA-MG)
Recruiting NCT04235335 - Healing Circles: An Intervention for Canadian Indigenous Mothers & Children Affected by IPV N/A