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Clinical Trials/NCT01925807
NCT01925807
Completed
Not Applicable

Brief Group Intervention for Adolescents With Mild to Moderate Suicidal Ideation and Their Caregivers: Preliminary Investigation for a Novel Treatment Approach

Allison Kennedy1 site in 1 country76 target enrollmentFebruary 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Suicidal Ideation
Sponsor
Allison Kennedy
Enrollment
76
Locations
1
Primary Endpoint
Suicidal Ideation
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Suicide is the second leading cause of mortality for Canadian adolescents. Mental health complaints are one of the leading reasons for an emergency department visit at the Children's Hospital of Eastern Ontario and 60% of adolescents report suicidal ideation. The goal of the present investigation is to test the efficacy of a brief group intervention for adolescents with passive suicidal ideation and their caregivers that will focus on coping, familial support, and emotional regulation. The investigators hypothesize that a brief group intervention, delivered in the weeks following presentation for crisis services, will reduce suicidal ideation and improve coping and familial support.

Registry
clinicaltrials.gov
Start Date
February 2014
End Date
May 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Allison Kennedy
Responsible Party
Sponsor Investigator
Principal Investigator

Allison Kennedy

Psychologist

Children's Hospital of Eastern Ontario

Eligibility Criteria

Inclusion Criteria

  • Mild to moderate suicidal ideation
  • Recently presented for services in response to a psycho-social crisis (Emergency Department, MH Urgent Care)
  • One or two caregiver(s) committed to attending the majority of sessions

Exclusion Criteria

  • Presence of a suicidal plan and/or recent gesture/attempt
  • Psychosis
  • Schizophrenia
  • Dual diagnosis
  • Developmental disability or delay
  • "Behavioural problem" as primary concern
  • Major substance abuse
  • Currently receiving mental health services (once every two weeks or more frequently)
  • Inability to commit to majority of sessions (minimum 4 of 6 sessions)
  • Children's aid society involvement

Outcomes

Primary Outcomes

Suicidal Ideation

Time Frame: 6 weeks

Suicidal ideation will be measured using the Suicidal Ideation Questionnaire Junior (SIQ-JR; Reynolds, 1988). Repeated Measures ANOVA or ANCOVA will be used to compare differences in suicidal ideation within groups (pre-post changes). Further comparisons using clinical cut-off will be conducted via McNemar test for matched pairs.

Secondary Outcomes

  • Familial Support(6 weeks)

Study Sites (1)

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