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Clinical Trials/NCT07402265
NCT07402265
Not yet recruiting
Not Applicable

Piloting a Brief, Online Intervention for Suicidality in Sexual and Gender Minority Youth

Western University0 sites250 target enrollmentStarted: February 1, 2026Last updated:
InterventionsKindMind

Overview

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
250
Primary Endpoint
Suicidal Ideation Questionnaire - Junior

Overview

Brief Summary

Sexual and gender minority youth (i.e., LGBTQ+ individuals) are at elevated risk for suicidal thoughts compared to cisgender/heterosexual youth and there is increased demand for programs and treatments tailored to this population. The current study seeks to pilot a brief, online, self-guided intervention for suicidal thoughts designed for sexual and gender minority youth to test if this intervention is acceptable to this population and if completing this intervention significantly decreases suicidal thoughts.

Detailed Description

The current study will pilot an intervention for suicidal thoughts in sexual and gender minority youth. We will recruit of a sample of sexual and gender minority youth who report experiencing recent thoughts of suicide. Participants will be asked to complete a battery of questionnaires including demographic questions and mental health symptom assessments, then complete the intervention, and finally complete additional questionnaires. One month after completing the intervention, participants will be asked to complete a series of questionnaires. This study is designed to evaluate the acceptability and initial effectiveness of this intervention and will not include a control group.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
13 Years to 25 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Resident of Canada
  • Fluent in English
  • Youth (i.e., 13-25 years)
  • Identifies as a sexual and/or gender minority (i.e., any sexual identity excluding heterosexual and/or any gender identity excluding cisgender)
  • Endorses experiencing any suicidal ideation within the past 6 months
  • Access to a computer and able to participate virtually

Exclusion Criteria

  • Does not meet the inclusion criteria

Arms & Interventions

Intervention Group

Experimental

Participants will complete the online, self-guided program, which will take approximately 30 minutes and involve participants completing modules describing how to use self-compassion/self-neutrality techniques to reduce suicidal thoughts.

Intervention: KindMind (Behavioral)

Outcomes

Primary Outcomes

Suicidal Ideation Questionnaire - Junior

Time Frame: From Baseline (i.e., before intervention administration) to four weeks after intervention administration.

Suicidal Ideation Questionnaire - Junior (SIQ-Jr; Reynolds, 1987). The SIQ-Jr was used to assess suicidal ideation in the current study. This self-report measure include 15 items of suicidal thoughts that are rated on a 7-item scale (i.e., Almost every day, couple of times a week, about once a week, couple of times a month, About once a month, I had this thought before but not in the past month, I never had this thought) of how frequency the respondent had each thought in their mind over the past month. Sample items include I thought about dying, I wished I were dead, and I thought about killing myself. The SIQ-Jr is scored by summing the responses to create a total score from 0-90, with higher scores indicating a higher severity of suicidal ideation.

Secondary Outcomes

  • Suicidal Ideation Thoughts and Behaviours Interview - Revised(From Baseline (i.e., before intervention administration) to four weeks after intervention administration.)
  • Self-Compassion Scale - Short Form(From Baseline (i.e., before intervention administration) to four weeks after intervention administration.)
  • Patient Health Questionnaire - 9(From Baseline (i.e., before intervention administration) to four weeks after intervention administration.)
  • Hopelessness Scale for Children(From Baseline (i.e., before intervention administration) to four weeks after intervention administration.)
  • Generalized Anxiety Disorder - 7(From Baseline (i.e., before intervention administration) to four weeks after intervention administration.)
  • Difficulties in Emotion Regulation Scale - Short Form(From Baseline (i.e., before intervention administration) to four weeks after intervention administration.)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Lindsay P. Bodell, PhD

Associate Professor

Western University

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