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Clinical Trials/NCT05935345
NCT05935345
Completed
Not Applicable

Addressing Nonsuicidal Self-injury in Schools

Region Östergötland1 site in 1 country267 target enrollmentJanuary 10, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Nonsuicidal Self-injury
Sponsor
Region Östergötland
Enrollment
267
Locations
1
Primary Endpoint
Frequency of nonsuicidal self-injury
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The aim of this study is to study the effectiveness of a whole-school approach that addresses non-suicidal self-injury and targets adolescents, parents and teachers. Whether training and interventions can influence NSSI will be examined. Furthermore, investigations will be conducted to examine whether this whole-school approach can reduce symptoms of mental health problems in adolescents, reduce stigma och increase help-seeking and perception of social support. Using a clustered waitlist control design, six lower secondary schools were randomized to either intervention or waitlist during four months (control groups were then given the intervention). Measures of NSSI, suicidality, mental well-being, stigma, attitudes, help-seeking and perceived social support were administered at baseline, after the intervention and at 6, 12 and 18-months follow-up. Two hundred and sixty-seven adolescents in seventh and eight grade participated in the study (135 active group and 132 control group). The interventions were delivered during four months. For adolescents, interventions were delivered in the class room and consisted of five sessions of the Youth Aware of Mental Health (YAM) program and one additional session focusing specifically on knowledge, stigma and attitudes toward NSSI (KRAS). Parents were offered an online psychoeducation on NSSI, as were all school staff during this time period. School health care personnel, nurses, psychologist and counsellors and other school staff, such as teachers' aids, support staff and mentors took part in a 2-day workshop on NSSI and suicidality.

Registry
clinicaltrials.gov
Start Date
January 10, 2022
End Date
June 12, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Maria Zetterqvist

Principal investigator

Region Östergötland

Eligibility Criteria

Inclusion Criteria

  • being a student in grade 7 and 8 in lower secondary school

Exclusion Criteria

  • special classes for refugees recently arrived in Sweden with insufficient knowledge of the Swedish language
  • special classes for adolescents with intellectual disability

Outcomes

Primary Outcomes

Frequency of nonsuicidal self-injury

Time Frame: Change from baseline at 4 months and at 6, 12 and 18 months

Change in self-reported frequency of nonsuicidal self-injury (NSSI) is measured with NSSI checklist from the Inventory of Statements About Self-injury (ISAS). Number of NSSI incidence is registered from 0 to the highest number that participants rate. High scores indicate more frequent NSSI.

Life-time prevalence of nonsuicidal self-injury

Time Frame: Change from baseline at 4 months and at 6, 12 and 18 months

Change in self-reported life-time prevalence of nonsuicidal self-injury is measured with a single-item (yes/no) from the Self-Injurious Thoughts and Behaviors Interview Self-Report Short-Form (SITBI-SR-SF).

Secondary Outcomes

  • Health-related quality of life(Change from baseline at 4 months and at 6, 12 and 18 months)
  • nonsuicidal self-injury expectancy(Change from baseline at 4 months and at 6, 12 and 18 months)
  • Perceived Social Support(Change from baseline at 4 months and at 6, 12 and 18 months)
  • Help-seeking(Change from baseline at 4 months and at 6, 12 and 18 months)
  • Stigma(Change from baseline at 4 months and at 6, 12 and 18 months)
  • Suicidal ideation(Change from baseline at 4 months and at 6, 12 and 18 months)

Study Sites (1)

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