Clinical Trial: Managing Inflammatory Bowel Disease

Study Status: Completed
Recruit Status: Completed
Study Type: Interventional

Official Title: Psychosocial Intervention for Children With IBD

Brief Summary: Inflammatory Bowel Disease (Crohn's disease and ulcerative colitis) often results in significant life disruption, hospitalization and surgery. While psychosocial factors are not believed to cause IBD, such factors can contribute to the ability of individuals with IBD to cope with the disease, and ineffective coping may lead to the exacerbation of IBD symptoms. The goal of this study is to evaluate the efficacy of a social learning and cognitive behavior therapy approach for treating children with IBD. The primary outcomes of interest are IBD symptoms, medical visits, quality of life, and overall disability.

Detailed Summary: Inflammatory Bowel Disease (Crohn's and ulcerative colitis; IBD), a serious medical condition that affects children and adolescents, is often associated with high rates of health care utilization and disability, including school absences. While psychosocial factors are not believed to cause IBD, research suggests that they may increase illness-related dysfunction. Prior studies suggest that response to chronic illness is, in part, acquired during childhood through social learning processes and may be modified with psychosocial interventions. This randomized controlled trial will compare a social learning and cognitive behavior therapy (SLCBT) treatment to an education and support condition (ES). 180 children with IBD will be recruited and followed for 12 months. It is hypothesized that SLCBT participants, compared to those in the ES condition, will, at one-year follow-up: 1) exhibit greater decreases in IBD symptoms, medical visits for IBD, and functional disability, and greater increases in quality of life; 2) demonstrate greater use of cognitive coping, relaxation and stress management skills, and their parents will demonstrate greater reductions in maladaptive responses to illness behavior; and 3) exhibit greater reductions in anxiety, depression, and somatization. Results will lead to innovative interventions for IBD and other chronic childhood medical conditions.
Sponsor: University of Washington

Current Primary Outcome: Functional Disability Inventory [ Time Frame: Baseline (1 week pre-treatment), 1 week post-treatment, 3 months, 6 months and 12-months post-treatment ]

Original Primary Outcome: Same as current

Current Secondary Outcome:

  • School absences [ Time Frame: Baseline, 3 months, 6 months and 12 months post-treatment ]
  • Health care utilization for IBD [ Time Frame: Baseline, 3 months, 6 months and 12 months post-treatment ]
  • Pediatric Quality of Life [ Time Frame: Baseline (1 week pre-treatment), 1 week post-treatment, 3 months, 6 months and 12 months post-treatment ]


Original Secondary Outcome: Same as current

Information By: University of Washington

Dates:
Date Received: May 14, 2008
Date Started: September 2007
Date Completion:
Last Updated: April 14, 2015
Last Verified: April 2015