Evaluation of the Child and Family Traumatic Stress Intervention (CFTSI)

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Yale University

Status and phase

Completed
Phase 2
Phase 1

Conditions

Posttraumatic Stress Disorder

Treatments

Behavioral: Child and Family Traumatic Stress Interv (CFTSI)
Behavioral: Psychoeducational Comparison

Study type

Interventional

Funder types

Other

Identifiers

NCT01031615
SAMHSA U79SM54318 (Other Grant/Funding Number)
0504027679

Details and patient eligibility

About

The purpose of this study is to determine the efficacy of the Child and Family Traumatic Stress Intervention (CFTSI) in preventing the development of Posttraumatic Stress Disorder (PTSD) when implemented within 30 days of a potentially traumatic event.

Enrollment

112 patients

Sex

All

Ages

7 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Youth exposed to a potentially traumatic event within the last 30 days who have one new symptom on the Posttraumatic Checklist (PCL)

Exclusion criteria

  • Already receiving mental health treatment
  • Autism or Developmental Disability
  • Diagnosed with psychosis or bipolar disorder
  • Non-english speaking

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

112 participants in 2 patient groups

Child and Family Traumatic Stress Interv
Experimental group
Description:
4-session secondary prevention model that focuses on family communication about symptoms of a child aged 7-16.
Treatment:
Behavioral: Child and Family Traumatic Stress Interv (CFTSI)
Psychoeducational Comparison
Active Comparator group
Description:
4-sessions focused on individual child using psychoeducation and relaxation skills
Treatment:
Behavioral: Psychoeducational Comparison

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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