NCT07818863

Brief Summary

This pilot study examines the feasibility, acceptability, and preliminary outcomes of a short-term group psychotherapy intervention for adolescents experiencing suicidal symptoms without immediate suicidal intent. The intervention is implemented within a public child and adolescent mental health clinic and includes emotional processing, interpersonal work, psychoeducation, and parental involvement. The study will evaluate participant engagement, attendance, and preliminary changes in suicidal ideation and related emotional and interpersonal functioning. The goal of the study is to contribute to the development of safe, feasible, and accessible group-based interventions for adolescents at suicide risk within public mental health services.

Trial Health

65
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
19mo left

Started Nov 2026

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 26, 2026

Completed
4 months until next milestone

First Posted

Study publicly available on registry

September 14, 2026

Completed
2 months until next milestone

Study Start

First participant enrolled

November 1, 2026

Expected
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2027

6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2028

Last Updated

September 14, 2026

Status Verified

September 1, 2026

Enrollment Period

1.1 years

First QC Date

May 26, 2026

Last Update Submit

September 9, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • Suicidal Ideation - Suicidal Ideation Questionnaire (SIQ)

    Suicidal ideation will be assessed using the Suicidal Ideation Questionnaire (SIQ), a self-report measure assessing the frequency and intensity of suicidal thoughts.

    Baseline and immediately post-intervention (after completion of the 8-session intervention)

  • Suicidal Ideation - Scale for Suicide Ideation (SSI)

    Suicidal ideation will be assessed using the Scale for Suicide Ideation (SSI), which assesses cognitive and motivational aspects of suicidal ideation, including planning, wish to die, and perceived ability to act.

    Baseline and immediately post-intervention (after completion of the 8-session intervention)

Study Arms (1)

Circles of Hope Group Intervention

EXPERIMENTAL

Participants will receive a short-term group psychotherapy intervention designed for adolescents experiencing suicidal symptoms without immediate suicidal intent. The intervention includes emotional processing, interpersonal group work, psychoeducational components, ongoing risk monitoring, and parental involvement within a public child and adolescent mental health clinic.

Behavioral: Circles of Hope Group Psychotherapy

Interventions

A short-term group psychotherapy intervention for adolescents experiencing suicidal symptoms without immediate suicidal intent. The intervention includes emotional processing, interpersonal group work, psychoeducational components, ongoing risk monitoring, and parental involvement within a public child and adolescent mental health clinic.

Circles of Hope Group Intervention

Eligibility Criteria

Age12 Years - 18 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Adolescents aged 12-18 years
  • Presence of suicidal symptoms or suicidal ideation
  • Ability to participate in a group psychotherapy intervention
  • Ability to provide informed assent and parental consent

You may not qualify if:

  • Immediate suicidal intent requiring urgent hospitalization or intensive intervention
  • Acute psychotic symptoms or severe cognitive impairment interfering with group participation
  • Clinical condition preventing participation in a group setting, as determined by clinical assessment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Suicidal Ideation

Condition Hierarchy (Ancestors)

SuicideSelf-Injurious BehaviorBehavioral SymptomsBehavior

Central Study Contacts

Chen Mike, PhD Candidate

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: Participants will receive a short-term group psychotherapy intervention delivered in small groups within a public child and adolescent mental health clinic. All participants will receive the same intervention, and outcomes will be assessed at baseline, post-intervention, and follow-up.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 26, 2026

First Posted

September 14, 2026

Study Start (Estimated)

November 1, 2026

Primary Completion (Estimated)

December 1, 2027

Study Completion (Estimated)

June 1, 2028

Last Updated

September 14, 2026

Record last verified: 2026-09

Data Sharing

IPD Sharing
Will not share