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Clinical Trials/NCT01606514
NCT01606514CompletedNot Applicable

Web-based Intervention for Disaster-Affected Youth and Families

Medical University of South Carolina0 sites2,000 target enrollmentStarted: December 1, 2010Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
2,000
Primary Endpoint
Change in parent-child relationship quality

Study Overview

Brief Summary

A single disaster, terrorist attack, or other large-scale incident can adversely affect thousands of youth and families. Immediate consequences may include unmet basic needs and high economic burden, particularly among underserved populations. Disasters also can dramatically affect family roles and relationships over time (e.g., family routines, marital stress, parent-child interactions). Whereas most youth are resilient in the aftermath of disasters (i.e., do not develop serious mental health or health-risk problems), the prevalence of various problems of public health significance (e.g., PTSD, depression, substance abuse) clearly increases in this population. This underscores the need for effective, widely accessible, culturally-appropriate and cost-efficient interventions that foster resilience or rapid recovery relative to the health effects of disasters. Yet, few evidence-informed resources are available to youth and families to facilitate post-disaster resilience and recovery. Primary aims of this project are: (a) to develop a Web-based intervention for disaster-affected adolescents and parents targeting prevalent health-related correlates of disasters (i.e., development phase), (b) to conduct a randomized controlled population-based study to examine feasibility and preliminary efficacy of the intervention (i.e., randomized controlled trial [RCT] phase) and cultural relevance (i.e., perceived applicability of the intervention to one's cultural group), and (c) to refine the intervention based on RCT-phase data.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Factorial
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
12 Years to — (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •adolescent between the ages of 12-17 and primary caregiver,
  • •residence in study identified location(s) at time of disaster,
  • •home internet connectivity

Exclusion Criteria

  • •adolescent's primary caregiver not available,
  • •no adolescents in home,
  • •not residing in location at time of disaster,
  • •poor or no internet connectivity

Arms & Interventions

Child, Parenting, & Parent Web-Intervention

Experimental

Bounce Back Now Child, Parenting, & Parent Psychoeducation & Self-Help Web-Intervention.

Intervention: Bounce Back Now Website (Behavioral)

Child & Parenting Web-Intervention

Experimental

Bounce Back Now Child & Parenting Psychoeducation and Self-Help Web-Intervention.

Intervention: Bounce Back Now Website (Behavioral)

Child & Parent Web-based Assessment

No Intervention

Bounce Back Now Web-Based Symptom Assessment

Outcomes

Primary Outcomes

Change in parent-child relationship quality

Time Frame: baseline, 4 month followup, 12 month followup

Change in adolescent mental health symptoms

Time Frame: baseline, 4 month followup, and 12 month followup

Change in parent mental health symptoms

Time Frame: baseline, 4 month followup, 12 month followup

Change in parent-child conflict

Time Frame: baseline, 4 month followup, 12 month followup

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

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