Violence, DomesticSONVAWNCT05417919
Solution-oriented Nursing in Violence Against Women (SONVAW)
A study testing Solution-oriented Nursing in Violence Against Women (SONVAW) in people with Violence, Domestic, run by Muş Alparslan University at 1 site in Turkey (Türkiye).
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. Read more about this study
- Who is it for?
- Ages 14 to 20 yearsHealthy volunteers can take part
- Conditions the study is for
- Violence, Domestic
- What is being tested?
- Solution-oriented Nursing in Violence Against Women (SONVAW)
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 78 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 2 Nov 2021to 1 Jun 2022
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 14 to 20 years
- All sexes
- Healthy volunteers accepted
- Child, Adult
Who may be able to join
- be between the ages of 14-20
- continue high school education
- Not having cognitive, affective and mental limitations
- Not having any problems with hearing and vision skills
- Volunteering to participate in research
Who cannot join
- failure to meet inclusion criteria
Trial locations and contacts
1 site in 1 country.
About this study
Official title: The Effect of Solution-Focused Approach on Attitudes to Violence Against Women in High School Students
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.
Read the detailed 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.
- Conditions
- Violence, Domestic
- Being tested
- Solution-oriented Nursing in Violence Against Women (SONVAW)
- Keywords
- Solution-oriented approach, ,, violence against women,, high school students, psychiatric nurse
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Solution-oriented Nursing in Violence Against Women (SONVAW)Other
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
| Study group | Role | What they receive |
|---|---|---|
| Solution-oriented Nursing in Violence Against Women (SONVAW) | Experimental | 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. Receives: Other: Solution-oriented Nursing in Violence Against Women (SONVAW) |
| Control | No intervention | 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. |
What is being measured
The primary outcome is the main question the study is designed to answer.
violence against women
Before the start of the program, 45 students in the experimental group and 45 students in the control group were given the İSKEBE scale.
Measured: before the program
Secondary outcomes (3)
violence against women
A solution-oriented approach program was applied to the students who in the experimental group.
Measured: During the 6-week program
violence against women
Immediately after the end of the solution-oriented program, 45 students in the experimental group and 45 students in the control group were given the ISKEBE scale.
Measured: End of 6-week solution-oriented program
violence against women
45 students in the experimental group and 45 students in the control group were given the İSKEBE scale.
Measured: 3 months after the end of the solution-oriented approach program
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Jun 2022
- Study start2 Nov 2021
- Primary completion11 Mar 2022
- Study completion1 Jun 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Violence, DomesticStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 78 participants (actual)
Sponsor and investigators
- Lead sponsor
- Muş Alparslan University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Fatih Sahin, Muş Alparslan University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05417919
- Sponsor's protocol ID
- 0058
- Acronym
- SONVAW
- Status last verified
- Jun 2022
- First submitted
- 1 Jun 2022
- Last updated
- 14 Jun 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 14 Jun 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Solution-Focused Approach on Attitudes to Violence Against Women in High School Students
- ClinicalTrials.gov ID
- NCT05417919
- Acronym / sponsor ID
- SONVAW / 0058
- Conditions
- Violence, Domestic
- Keywords
- Solution-oriented approach, ,, violence against women,, high school students, psychiatric nurse
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 78 participants (actual)
- Lead sponsor
- Muş Alparslan UniversityUniversity, hospital or other
- Study start
- 2 Nov 2021 (actual)
- Primary completion
- 11 Mar 2022 (actual)
- Study completion
- 1 Jun 2022 (actual)
- First posted
- 14 Jun 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed 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
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Solution-oriented Nursing in Violence Against Women (SONVAW) | Experimental | Other: Solution-oriented Nursing in Violence Against Women (SONVAW)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. |
| Control | No intervention | –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. |
Who may qualify
- Ages
- 14 to 20 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
Key inclusion criteria (5 listed)
- be between the ages of 14-20
- continue high school education
- Not having cognitive, affective and mental limitations
- Not having any problems with hearing and vision skills
- Volunteering to participate in research
Key exclusion criteria (1 listed)
- failure to meet inclusion criteria
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Solution-oriented Nursing in Violence Against Women (SONVAW)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 | Other | Solution-oriented Nursing in Violence Against Women (SONVAW) |
Primary outcome
violence against women
Time frame: before the program
Before the start of the program, 45 students in the experimental group and 45 students in the control group were given the İSKEBE scale.
3 secondary outcomes
violence against women
Time frame: During the 6-week program
violence against women
Time frame: End of 6-week solution-oriented program
violence against women
Time frame: 3 months after the end of the solution-oriented approach program
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Jun 2022.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Solution-oriented Nursing in Violence Against Women (SONVAW) in people with Violence, Domestic, run by Muş Alparslan University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 14 Jun 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
violence against women (time frame: before the program). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Jun 2022.