ClinicalTrials.gg
Not yet recruitingNCT07722455Updated Jul 23, 2026

Hand in Hand, We Rise (Xie Shou Gong Jin)

An interventional study of Xie Shou Gong Jin and Regular psychoeducation class in Suicide, Suicide Awareness and Mental Health, sponsored by Brown University. Not yet recruiting at 1 site in China. Open to participants aged 11 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-23.

Primary conditionSuicide PreventionRegistry: SuicideReclassifiedWhy we changed it
Registry
Suicide — the first condition term the registry derived for this study.
ClinicalTrials.gg
Suicide Prevention
Why
  1. Suicide is a broad heading, used only when no more specific condition is named.
  2. The study's listed conditions name Suicide Prevention, a narrower term within Suicide.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Brown University · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
1,680
Allocation
Randomized
Ages
11 Years and older
Sex
All
01

Study summary

This study aims to conduct a cluster randomized controlled trial to assess the feasibility of implementing the "Hand in Hand, We Rise" (Xie Shou Gong Jin) multi-stakeholder collaborative school-based suicide prevention program in rural public junior high schools. Six schools will be randomly assigned in a 1:1 ratio to either the intervention group or the control group; the intervention group will simultaneously implement the "Youth Strengths \& Skills Curriculum (YSSC)" curriculum for students, "Life Gatekeeper" training for teachers, and mental health information dissemination for caregivers. The primary objectives are to evaluate recruitment, retention, adherence, implementation fidelity, acceptability, and safety within real-world school settings, and to preliminarily estimate changes in indicators such as suicidal ideation, depression, anxiety, loneliness, help-seeking attitudes, mental health stigma, self-esteem, school climate, and bullying. The findings will provide parameters and an implementation basis for a subsequent large-scale, multi-school cluster randomized controlled trial.

02

Conditions studied

  • Suicide
  • Suicide Awareness
  • Mental Health
  • Suicide Prevention

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03

In context

Suicide Prevention Reclassified

186 studies on the registry are indexed under Suicide Prevention; 92 are open to participants now.

This study's planned enrollment of 1,680 is above the median of 140 across 167 interventional studies indexed under Suicide Prevention.

Browse Suicide Prevention studies →

Lead sponsor

Brown University is the lead sponsor of 290 studies on the registry; 40 are open to participants now.

Of its 26 completed or terminated interventional studies of FDA-regulated products, 19 (73%) have results posted.

Compared within Suicide Prevention, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Suicide. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
11 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adolescent inclusion criteria include: (a) is a registered student at one of the participating schools, (b) be between the ages of 11-15, (c) fluent in reading Chinese during the consent process, (d) be willing to participate in the YSSC curriculum during their psychoeducation class.
  • Caregiver inclusion criteria include: (a) age 18 or above, (b) can read and speak Chinese, (c) be a primary caregiver of an adolescent enrolled in the participating schools, and (d) willing to discuss perceived needs related to adolescent suicide prevention.
  • Teacher inclusion criteria include: (a) age 18 or above, (b) can read and speak Chinese, (c) be a full-time teacher of the participating schools.

Exclusion criteria

Exclusion Criteria:

  • Individuals will be excluded from the study if they are determined to have symptoms that would prevent them from giving meaningful consent or participate in study activities, such as significant cognitive impairment.
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Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
1,680 participants (estimated)

Study arms

  • Experimental
    Hand in Hand, We Rise

    Six schools will be randomly assigned in a 1:1 ratio to either the intervention group or the control group; the intervention group will simultaneously implement the "Youth Strengths \& Skills Curriculum (YSSC)" curriculum for students, "Life Gatekeeper" training for teachers, and mental health information dissemination for caregivers. Students' intervention (YSSC) includes a 6-session course, with each session delivered by school mental health teachers approximately every 2 weeks. Parents' intervention also includes 6-lesson course, with each lesson delivered approximately every 2 weeks. Teachers' intervention will be a 1-to-2-day(s) training delivered right after the randomization.

    Behavioral: Xie Shou Gong Jin

  • Active comparator
    Usual care

    Psychoeducation classroom education for students as usual

    Behavioral: Regular psychoeducation class

Interventions

  • BehavioralXie Shou Gong Jin

    Six schools will be randomly assigned in a 1:1 ratio to either the intervention group or the control group; the intervention group will simultaneously implement the "Youth Strengths \& Skills Curriculum (YSSC)" curriculum for students, "Life Gatekeeper" training for teachers, and mental health information dissemination for caregivers.

  • BehavioralRegular psychoeducation class

    Psychoeducation classroom as usual in schools, provided by teachers to students as part of the regular school curriculum

06

What researchers measure

Primary outcomes

  1. Suicide Ideation Attributes Scale (SIDAS)

    Frequency and severity of suicide ideation will be evaluated by SIDAS at baseline, 4 months and 8 months follow-up to evaluate suicide ideation as one of the primary outcomes among adolescents.

    Time frame: Baseline, 4 months (post-intervention) and 8 months follow-up

  2. Columbia-Suicide Severity Rating Scale (C-SSRS)

    Severity of suicide risk will be assessed by the Columbia-Suicide Severity Rating Scale (C-SSRS) at baseline, 4 months and 8 months follow-up to evaluate the overall risk of suicide as one of the primary outcomes among adolescents.

    Time frame: Baseline, 4 months (post-intervention) and 8 months follow-up

  3. Session Evaluation Form (SEF)

    The 13-item SEF measuring perceived feasibility, acceptability, and intervention utility of the intervention at 4 months follow-up/postintervention

    Time frame: 4 months (post-intervention)

  4. Client Satisfaction Survey (CSQ-8)

    The 8-item CSQ assessing satisfaction will be used to measure intervention acceptability at 4 months follow-up/post-intervention.

    Time frame: 4 months (post-intervention)

Secondary outcomes

  1. Patient Health Questionnaire (PHQ-9)

    Severity of depression as a secondary outcome will be measured by the Patient Health Questionnaire (PHQ-9) at baseline, 4 months and 8 months follow-up among adolescents.

    Time frame: Baseline, 4 months (post-intervention) and 8 months follow-up

  2. Generalized Anxiety Disorder (GAD-7)

    Severity of anxiety symptoms as a secondary outcome will be measured by the Generalized Anxiety Disorder (GAD-7), at baseline, 4 months and 8 months follow-up among adolescents.

    Time frame: Baseline, 4 months (post-intervention) and 8 months follow-up

  3. Attitudes Toward Seeking Professional Psychological Help

    Help-seeking attitude will be measured by the Attitudes Toward Seeking Professional Psychological Help, at baseline, 4 months and 8 months follow-up among adolescents, caregivers, and school teachers.

    Time frame: Baseline, 4 months (post-intervention) and 8 months follow-up

  4. Perceived Devaluation Discrimination (PDD) scale

    Perception of stigma against mental health will be measured by the Perceived DevaluationDiscrimination (PDD) scale, as a secondary outcome, at baseline, 4 months and 8 months follow-up among adolescents, caregivers, and school teachers.

    Time frame: Baseline, 4 months (post-intervention) and 8 months follow-up

  5. Stigma of Suicide Scale (SOSS)-short form

    Stigma against suicide will be measured by Stigma of Suicide Scale (SOSS)-short form, as a secondary outcome, at baseline, 4 months and 8 months follow-up among adolescents, caregivers, and school teachers.

    Time frame: Baseline, 4 months (post-intervention) and 8 months follow-up

  6. Adapted Delaware School Climate Survey

    Peer bullying will be measured by the Adapted Delaware School Climate Survey, as a secondary outcome, at baseline, 4 months and 8 months follow-up among adolescents.

    Time frame: Baseline, 4 months (post-intervention) and 8 months follow-up

  7. Rosenberg Self-Esteem Scale

    The 10-item Rosenberg Self-Esteem Scale will be used to assess self-esteem as a secondary outcome at baseline, 4 months (post-intervention) and 8 months follow-up. This scale will be assessed among adolescents.

    Time frame: Baseline, 4 months (post-intervention) and 8 months follow-up

  8. Suicide Prevention Gatekeeper Self-Efficacy Scale (GKSES)

    The Suicide Prevention Gatekeeper Self-Efficacy Scale (GKSES) will be used to assess self-efficacy among teachers and caregivers as a secondary outcome at baseline, 4 months (post-intervention) and 8 months follow-up.

    Time frame: Baseline, 4 months (post-intervention) and 8 months follow-up

  9. Brief Difficulties in Emotion Regulation Scale (DERS-16)

    The 16-item Brief Difficulties in Emotion Regulation Scale (DERS-16) will be used to assess difficulties in emotion regulation as a secondary outcome at baseline, 4 months (post-intervention) and 8 months follow-up among adolescents.

    Time frame: Baseline, 4 months (post-intervention) and 8 months follow-up.

  10. WHO-5 Well-Being Index

    The subjective psychological well-being will be measured by WHO-5 Well-Being Index as a secondary outcome at baseline, 4 months (post-intervention) and 8 months follow-up among adolescents.

    Time frame: Baseline, 4 months (post-intervention) and 8 months follow-up

  11. Child and Adolescent Mindfulness Measure (CAMM)

    The 10-item Child and Adolescent Mindfulness Measure (CAMM) will be used to assess mindfulness as a secondary outcome among adolescents at baseline, 4 months (post-intervention) and 8 months follow-up.

    Time frame: Baseline, 4 months (post-intervention) and 8 months follow-up.

  12. Children's Hope Scale

    Hope will be measured by the 6-item Children's Hope Scale (CHS) as a secondary outcome among adolescents at baseline, 4 months (post-intervention) and 8 months follow-up.

    Time frame: Baseline, 4 months (post-intervention) and 8 months follow-up.

  13. Self-Compassion Scale Short Form

    Self-compassion among adolescents will be measured by the 12-item Self-Compassion Scale Short Form (SCS-SF) as a secondary outcome at baseline, 4 months (post-intervention) and 8 months follow-up.

    Time frame: Baseline, 4 months (post-intervention) and 8 months follow-up.

  14. Resilience Scale (CYRM-R)

    The 12-item Child and Youth Resilience Measure-Revised (CYRM-R) will be used to assess resilience as a secondary outcome at baseline, 4 months (post-intervention) and 8 months follow-up among adolescents.

    Time frame: Baseline, 4 months (post-intervention) and 8 months follow-up.

Other outcomes

  1. Adverse Childhood Experience

    Adverse childhood experience will be measured by baseline as a potential intervention effect moderator. This scale will be assessed among adolescents.

    Time frame: Baseline

07

Study locations

1 site
  • Six middle schools
    Linquan County, Anhui, China
08

References and documents

Individual participant data

Plan to share: Yes — Following data collection, cleaning, and analysis, we plan to publish de-identified quantitative data at an open science data repository (e.g., Open Science Framework). De-identified qualitative data will be available upon request to the study PI.

Supporting information: Study protocol, Statistical analysis plan

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Aug 2026; primary completion for Jul 2027, 11 months later.

Of 127 non-industry interventional studies with no phase under Suicide Prevention, half reached primary completion within 28 months of starting (the median), counting those still running; a quarter within 12 and three quarters within 53. This study's planned 11 months is below that.

Counting every sponsor, half of 129 studies reached it within 28 months; a quarter within 12 and three quarters within 53.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 20, 2026
First posted
Jul 23, 2026
StartEst.
Aug 2026
Primary completionEst.
Jul 2027
CompletionEst.
Jul 2027
Last update
Jul 23, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07722455
Lead sponsor
Brown University
Collaborators
Beijing Normal University
Responsible party
Sponsor
First posted
Jul 23, 2026
Start date
Aug 2026 (estimated)
Primary completion
Jul 2027 (estimated)
Completion
Jul 2027 (estimated)
Last update
Jul 23, 2026

Study contacts

Shufang Sun, PhD
Contact
flourishing@brown.edu
401-484-0012

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is not yet recruiting, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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