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Clinical Trials/NCT01606514
NCT01606514
Completed
Not Applicable

Web-based Intervention for Disaster-Affected Youth and Families

Medical University of South Carolina0 sites2,000 target enrollmentDecember 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Mental Health Wellness 1
Sponsor
Medical University of South Carolina
Enrollment
2000
Primary Endpoint
Change in parent-child relationship quality
Status
Completed
Last Updated
11 years ago

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.

Registry
clinicaltrials.gov
Start Date
December 2010
End Date
June 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

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

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