Addressing Nonsuicidal Self-injury in Schools

Sponsor

Region Östergötland (Other)

Overall Status

Completed

CT.gov ID

NCT05935345

Collaborator

(none)

267

Enrollment

Location

Arms

Actual Duration (Months)

15.7

Patients Per Site Per Month

Study Details

Study Description

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.

Condition or Disease	Intervention/Treatment	Phase
Nonsuicidal Self-injury Suicidal Ideation Stigmatization Help-Seeking Behavior Perceived Social Support Mental Well-being	Behavioral: Addressing NSSI in schools Other: Control condition	N/A

Study Design

Study Type:

Interventional

Actual Enrollment :

267 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Prevention

Official Title:

Addressing Nonsuicidal Self-injury in Schools

Actual Study Start Date :

Jan 10, 2022

Actual Primary Completion Date :

Jun 12, 2023

Actual Study Completion Date :

Jun 12, 2023

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Addressing NSSI in schools During the four months of active experimental condition, adolescents receive five sessions of the youth aware of mental health program in the class room, and one additional session on NSSI. Parents and school staff receive an online psychoeducation on NSSI. School health care personnel receive a 2-day workshop on NSSI and suicidality.	Behavioral: Addressing NSSI in schools During the four months of active experimental condition, adolescents receive five sessions of the youth aware of mental health program in the class room, and one additional session on NSSI. Parents and school staff receive an online psychoeducation on NSSI. School health care personnel receive a 2-day workshop on NSSI and suicidality.
Other: Control condition Participating adolescents, parents, teachers and school health care personnel receive no intervention during four months	Other: Control condition Participating adolescents, parents, teachers and health care personnel receive no intervention during four months

Arm

Intervention/Treatment

Experimental: Addressing NSSI in schools

During the four months of active experimental condition, adolescents receive five sessions of the youth aware of mental health program in the class room, and one additional session on NSSI. Parents and school staff receive an online psychoeducation on NSSI. School health care personnel receive a 2-day workshop on NSSI and suicidality.

Behavioral: Addressing NSSI in schools

Other: Control condition

Participating adolescents, parents, teachers and school health care personnel receive no intervention during four months

Other: Control condition

Participating adolescents, parents, teachers and health care personnel receive no intervention during four months

Outcome Measures

Primary Outcome Measures

Life-time prevalence of nonsuicidal self-injury [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).
Frequency of nonsuicidal self-injury [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.

Secondary Outcome Measures

Health-related quality of life [Change from baseline at 4 months and at 6, 12 and 18 months]
Change in self-reported health-related quality of life (HRQOL) is measured with the 52-item version of the kid screen (KIDSCREEN 52), a self-report measure that measures the subjective HRQOL in children and adolescents between the ages of 8 and 18. KIDSCREEN 52 questionnaire consisted of 52 items assessing ten HRQOL dimensions. The KIDSCREEN-52 HRQOL questionnaire assesses the frequency of behavior/feelings or and use a 5-point Likert response scale. Scores are computed for each dimension and are transformed into T-values with a mean of 50 and a standard deviation of 10. Higher scores indicate higher HRQOL.
nonsuicidal self-injury expectancy [Change from baseline at 4 months and at 6, 12 and 18 months]
Change in self-reported nonsuicidal self-injury expectancy is measured with the Non-Suicidal Self-Injury Expectancy Questionnaire (NEQ), which is a self-report measure that measures attitudes and expectancy to own and others' NSSI. A shortened 10-item version was used with items scored on a 4-point Likert scale, ranging from 10 to 40, with higher scores indicating higher endorsement of NSSI expectancies.
Perceived Social Support [Change from baseline at 4 months and at 6, 12 and 18 months]
Change in self-reported perceived social support was measured using the Multidimensional Scale of Perceived Social Support, which is a self-report scale that measures perceived social support. It contains 12 items and is scored on a 7-point Likert scale with total scores ranging from 12 to 84, with higher scores indicating higher levels of perceived social support.
Stigma [Change from baseline at 4 months and at 6, 12 and 18 months]
Change in self-reported stigma is measures with the Mental Health Stigmatization Scale-Revised (PMHSS-R). PMHSS-R assess perceptions of stigma awareness and agreement related to mental-health in peers. The subscales include six and five items rated on a five-point Likert scale (1 = disagree completely, 5 = agree completely). An individual score is generated by adding up all items of each subscale, which ranges from 6 to 30 (awareness) and 5 to 25 (agreement). Higher scores indicate higher levels of stigma agreement and stigma awareness, that is, higher levels of mental health related stigmatizing attitudes.
Help-seeking [Change from baseline at 4 months and at 6, 12 and 18 months]
Change in self-reported help-seeking is measured with Help-Seeking Acceptability at School, Adult Help for Suicidal Youth and Reject Codes of Silence, which is a self-report measure that assesses attitudes toward seeking help from adults in three domains: "Help seeking acceptability", "Adult help for suicidal youth" and "Reject Codes of Silence". The total score includes 11 items which are scored on a 4-point Likert scale. Scores range from 4 to 16 (help-seeking acceptability); 3 to 12 (Adult help), and 3 to 12 (rejecting codes of silence). Higher scores indicate better outcome and a more positive attitude to help-seeking.
Suicidal ideation [Change from baseline at 4 months and at 6, 12 and 18 months]
Change in self-reported suicidal ideation is assessed with the Self-Injurious Thoughts and Behaviors Interview Self-Report Short-Form (SITBI-SR-SF) as single-item assessment of prevalence yes/no.

Other Outcome Measures

Difficulties in emotion regulation [Change from baseline at 4 months and at 6, 12 and 18 months]
Changes in self-reported difficulties in emotion regulation is measures with the 16-item version of the Difficulties in Emotion Regulation Scale (DERS-16). Total scores range from 16 to 80 with higher scores indicating higher levels of difficulties in emotion regulation.
Self-criticism [Change from baseline at 4 months and at 6, 12 and 18 months]
Change in self-reported self-criticism is measures using the Self-Rating Scale (SRS), which is a self-report measure to assess self-criticism. It contains of 8 items which are scored on a 7-point Likert scale. The total scale ranges from 8 to 56 with higher scores indicating higher levels of self-criticism.

Eligibility Criteria

Criteria

Ages Eligible for Study:

13 Years to 15 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

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