Suicidal ThoughtsNCT07402265
Piloting a Brief, Online Intervention for Suicidality in Sexual and Gender Minority Youth
A study testing KindMind in people with Suicidal Thoughts and Sexual and Gender Minorities, run by Western University at 1 site in Canada.
Trial 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. Read more about this study
- Who is it for?
- Ages 13 to 25 years
- Conditions the study is for
- Suicidal Thoughts, Sexual and Gender Minorities, Youth
- What is being tested?
- KindMind
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 250 participants
- Where
- 1 siteCanada
- Study dates
- 1 Feb 2026to 30 Sep 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 13 to 25 years
- All sexes
- No healthy volunteers
- Child, Adult
Who may be able to join
- 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
Who cannot join
- Does not meet the inclusion criteria
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Canada1 site, 1 recruiting
- Recruiting
Western University
London, Ontario
Lindsay Bodell, PhD, 519-661-2111 ext. x80486, lbodell@uwo.ca
Lindsay Bodell, PhD
About this study
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.
Read the 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.
- Conditions
- Suicidal Thoughts, Sexual and Gender Minorities, Youth
- Being tested
- KindMind
- Keywords
- Suicidal thoughts, Sexual and Gender Minorities, Youth, Brief, Online, Self-Guided, Self-Compassion, Self-Neutrality
- Medical subject headings
- Suicidal Ideation, Coitus
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
KindMindBehavioural
This intervention is hosted on Wix-com and involves multiple self-guided modules in which participants are taught how to use self-compassion and/or self-neutrality to reduce suicidal thoughts. This intervention is tailored to sexual and gender minority youth.
| Study group | Role | What they receive |
|---|---|---|
| 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. Receives: Behavioral: KindMind |
What is being measured
The primary outcome is the main question the study is designed to answer.
Suicidal Ideation Questionnaire - Junior
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.
Measured: From Baseline (i.e., before intervention administration) to four weeks after intervention administration.
Secondary outcomes (6)
Suicidal Ideation Thoughts and Behaviours Interview - Revised
Suicidal Ideation Thoughts and Behaviours Interview - Revised (SITBI -R; Gratch et al., 2022). Select items from the SITBI-R will be administered to capture suicidal behaviour, including frequency and severity of suicide attempts.
Measured: From Baseline (i.e., before intervention administration) to four weeks after intervention administration.
Self-Compassion Scale - Short Form
Self-Compassion Scale - Short Form (SCS-SF; Raes et al., 2011). The SCS-SF is a 12-item measure that assesses trait self-compassion. Each item is rated on a 5-point scale of how the participant typically reacts to themselves during difficult times, ranging from Almost never to Almost Always. Six subscales are computed corresponding to the six components of self-compassion based on Neff's (2003) conceptualization: Self-Kindness, Self-Judgement, Common Humanity, Isolation, Mindfulness, and Overidentification. A total score is computed by averaging the six subscale total scores. Higher scores indicated higher self-compassion. Sample items include I try to see my failing as part of the human condition and I'm disapproving and judgmental about my own flaws and inadequacies.
Measured: From Baseline (i.e., before intervention administration) to four weeks after intervention administration.
Patient Health Questionnaire - 9
Patient Health Questionnaire - 9 (PHQ-9; Kroenke et al., 2001). The PHQ-9 a self-report assessment of depressive symptoms. The PHQ-9 includes nine items that ask participants to rate how frequently they experienced each problem (i.e., Little interest or pleasure in doing things, Feeling tired or having low energy) over the past two weeks, with a 4-point scale of frequency (i.e., Not at all, Several days, More than half the days, Nearly every day). A total score is summed and can range from 0-27. Higher total scores indicate greater severity of depressive symptoms. An additional item not included in the total score asks participants to rate how difficult the problems they indicated make it for them to do work, take care of things at home, and get along with other people.
Measured: From Baseline (i.e., before intervention administration) to four weeks after intervention administration.
Hopelessness Scale for Children
Hopelessness Scale for Children (HSC; Kazdin et al., 1983). The HSC includes 17 true/false items assessing hopelessness in children as young as 5 years old. Total scores are summed and the higher the total score, the greater the hopelessness for the future. Sample items include I will have more good times than bad times and I don't think I will get what I really want.
Measured: From Baseline (i.e., before intervention administration) to four weeks after intervention administration.
Generalized Anxiety Disorder - 7
Generalized Anxiety Disorder - 7 (GAD-7; Spitzer et al., 2006) . The GAD-7 is a self-report assessment of anxiety. The respondent indicates how often they have experienced each of seven listed symptoms over the past two weeks, including items such as Not being able to stop or control worrying and Becoming easily annoyed or irritable. Items are rated on a 4-point scale of frequency (i.e., Not at all, Several days, More than half the days, Nearly every day). Total scores range from 0-21, with higher scores indicating higher severity of anxiety. An additional item not included in the total score asks participants to rate how difficult the problems they indicated make it for them to do work, take care of things at home, and get along with other people.
Measured: From Baseline (i.e., before intervention administration) to four weeks after intervention administration.
Difficulties in Emotion Regulation Scale - Short Form
Difficulties in Emotion Regulation Scale - Short Form (DERS-SF; Kaufman et al., 2016). The DERS-SF is a self-report measure of difficulties regulating emotion. This measure has 18 items that are rated on a 5-point scale assessing how often each item applies to the participant, including the following options: Almost never (0-10%), Sometimes (11-35%), About half of the time (36-65%, Most of the time (66-90%), and Almost always (91-100%). The DERS-SF includes items such as When I'm upset, I have difficulty concentrating and I pay attention to how I feel. A total score and six subscale scores (Strategies, Nonacceptance, Impulse, Goals, Awareness, Clarity) are created by adding item scores and higher scores reflect greater difficulties with emotion regulation. Total scores range from 18-90.
Measured: From Baseline (i.e., before intervention administration) to four weeks after intervention administration.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Feb 2026
- Study start1 Feb 2026
- Primary completion30 Sep 2026 (estimated)
- Study completion30 Sep 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Suicidal ThoughtsStudies 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
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- All participants will complete the same program. There is no control group.
- Masking
- None (open label)
- Enrolment
- 250 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Western University
- Sponsor type
- University, hospital or other
- Collaborators
- Western University, Canada, Social Sciences and Humanities Research Council of Canada
- Responsible party
- Principal investigator, Lindsay P. Bodell, PhD, Western University
- Investigators
- Lindsay P Bodell, PhD, Principal investigator, Western University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07402265
- Sponsor's protocol ID
- 127209
- Status last verified
- Feb 2026
- First submitted
- 30 Jan 2026
- Last updated
- 21 Aug 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Only de-identified IPD that is included in the published results of the study will be shared.
Study at a glance
From the registry record, last updated by the sponsor on 21 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Piloting a Brief, Online Intervention for Suicidality in Sexual and Gender Minority Youth
- ClinicalTrials.gov ID
- NCT07402265
- Acronym / sponsor ID
- 127209
- Conditions
- Suicidal Thoughts, Sexual and Gender Minorities, Youth
- Keywords
- Suicidal thoughts, Sexual and Gender Minorities, Youth, Brief, Online, Self-Guided, Self-Compassion, Self-Neutrality
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 250 participants (estimated)
- Lead sponsor
- Western UniversityUniversity, hospital or other
- Collaborators
- Western University, Canada, Social Sciences and Humanities Research Council of Canada
- Study start
- 1 Feb 2026 (actual)
- Primary completion
- 30 Sep 2026 (estimated)
- Study completion
- 30 Sep 2026 (estimated)
- First posted
- 11 Feb 2026 (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.
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
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- All participants will complete the same program. There is no control group.
| Arm | Type | Receives |
|---|---|---|
| Intervention Group | Experimental | Behavioral: KindMindParticipants 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. |
Who may qualify
- Ages
- 13 to 25 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult
Key inclusion criteria (6 listed)
- 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
Key exclusion criteria (1 listed)
- Does not meet the 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 |
|---|---|---|
| KindMindThis intervention is hosted on Wix-com and involves multiple self-guided modules in which participants are taught how to use self-compassion and/or self-neutrality to reduce suicidal thoughts. This intervention is tailored to sexual and gender minority youth. | Behavioural | Intervention Group |
Primary outcome
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.
6 secondary outcomes
Suicidal Ideation Thoughts and Behaviours Interview - Revised
Time frame: From Baseline (i.e., before intervention administration) to four weeks after intervention administration.
Self-Compassion Scale - Short Form
Time frame: From Baseline (i.e., before intervention administration) to four weeks after intervention administration.
Patient Health Questionnaire - 9
Time frame: From Baseline (i.e., before intervention administration) to four weeks after intervention administration.
Hopelessness Scale for Children
Time frame: From Baseline (i.e., before intervention administration) to four weeks after intervention administration.
Generalized Anxiety Disorder - 7
Time frame: From Baseline (i.e., before intervention administration) to four weeks after intervention administration.
Difficulties in Emotion Regulation Scale - Short Form
Time frame: From Baseline (i.e., before intervention administration) to four weeks after intervention administration.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Aug 2026.
- Individual participant dataSharing planned: Yes. Only de-identified IPD that is included in the published results of the study will be shared.
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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.
Lindsay P Bodell, PhD principal investigator
Western University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing KindMind in people with Suicidal Thoughts and Sexual and Gender Minorities, run by Western University at 1 site in Canada.
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 6 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: looking for participants now, as of the sponsor's last update on 21 Aug 2026. 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 Canada. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Genevieve M Bianchini, MSc (519-661-2111 ext. 87316, gbianch2@uwo.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Suicidal Ideation Questionnaire - Junior (time frame: From Baseline (i.e., before intervention administration) to four weeks after intervention administration.). 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 21 Aug 2026.