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Clinical Trials/NCT02610309
NCT02610309CompletedNot Applicable

Family-based Crisis Intervention With Suicidal Adolescents in the Emergency Department: A Randomized Clinical Trial

Boston Children's Hospital1 site in 1 country143 target enrollmentStarted: January 1, 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
143
Locations
1
Primary Endpoint
Disposition at discharge from the ED (psychiatric hospitalization or other)

Study Overview

Brief Summary

The Family Based Crisis Intervention (FBCI) is an emergency psychiatry intervention designed to sufficiently stabilize suicidal adolescents within a single ED visit so that they may return home safely with their families. This study is a randomized clinical trial of FBCI v. TAU in an urban Emergency Department.

Detailed Description

In current practice, treatment as usual (TAU) for suicidal adolescents includes evaluation, with little or no intervention provided in the Emergency Department (ED), and disposition, usually to an inpatient psychiatry unit. The Family Based Crisis Intervention (FBCI) is an emergency psychiatry intervention designed to sufficiently stabilize suicidal adolescents within a single ED visit so that they may return home safely with their families. The intervention works intensively with both the adolescent and the family, so that the caregiver has the knowledge and skills to help the adolescent after discharge.

In this study, suicidal adolescents (ages 13-18) and their families presenting for psychiatric evaluation to a large pediatric ED were randomized to receive FBCI or treatment as usual (TAU). Patients and caregivers completed self-report measures of suicidality, family empowerment, and satisfaction with care provided at pre-test, post-test, and 3 follow up time-points over a one-month period. Clinicians contacted the adolescent and caregiver at these timepoints to administer the questionnaires and assure safety planning was being carried out.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
13 Years to 18 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •adolescent presenting to the ED with suicidality
  • •presence of a consenting parent or legal guardian with whom the adolescent resided.

Exclusion Criteria

  • •either adolescent or parent/guardian lacked fluency in English;
  • •adolescent was not medically stable, including intoxication;
  • •adolescent demonstrated cognitive limitations prohibiting completion of research instruments;
  • •adolescent presented with active psychosis;
  • •adolescent required physical or medication restraint in the ED.

Arms & Interventions

Family-Based Crisis Intervention

Experimental

The Family-Based Crisis Intervention (FBCI) is a single-session intervention that takes place in the Emergency Department. Adolescents randomized to the experimental condition received a standard psychiatric evaluation followed by the experimental intervention. FBCI was administered by licensed psychiatric social workers who were trained in the intervention. The research clinician provided FBCI to the suicidal adolescent and his/her parent(s)/guardian(s) in a 60-90 minute session in which she helped the adolescent and family develop a joint crisis narrative of the problem and taught them cognitive-behavioral skill-building, therapeutic readiness, psycho-education about depression, and safety planning.

Intervention: Family-Based Crisis Intervention (Behavioral)

Treatment As Usual

No Intervention

Treatment as usual included an emergency psychiatry evaluation (standard care).

Outcomes

Primary Outcomes

Disposition at discharge from the ED (psychiatric hospitalization or other)

Time Frame: one day, one week, and one month

The primary outcome measure is disposition (psychiatric hospitalization vs. less restrictive level of care) after receiving the FBCI intervention or TAU. Psychiatric hospitalization was reassessed at 1 day, 1 week and 1 month intervals after randomization.

Secondary Outcomes

  • Client Satisfaction Questionnaire (CSQ-8)(one day)
  • Family Empowerment Scale (FES)(one month)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Elizabeth Wharff

Clinical Researcher

Boston Children's Hospital

Study Sites (1)

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