Abdominal Pain, Chronic Pain, Headache
Conditions
Keywords
cognitive-behavioral therapy, chronic pain, randomized controlled trial, pediatrics
Brief summary
The purpose of this study is to develop and evaluate the feasibility and effectiveness of a web-based (i.e., internet) treatment approach for providing psychological treatment to reduce pain and improve functioning in children and adolescents with chronic pain.
Detailed description
Chronic pain is an important problem for children and adolescents owing to its high prevalence rate and significant impact on children's mood, daily functioning, and overall quality of life. Effective psychological treatments have been developed to change behaviors and thoughts important in the child's ability to cope with chronic pain. However, the majority of children do not have access to these treatments due to a variety of barriers such as geographical distance from pediatric pain treatment centers. The purpose of this study is to develop a more accessible method of delivering effective psychological treatment to reduce pain and increase function in children. Children with chronic headache, abdominal, or musculoskeletal pain will be randomized to either receive the web-based treatment right away or to be in a wait-list control condition and receive the treatment 8 weeks later. Both groups of children will continue to receive clinical care through specialty medical clinics. Children's level of pain, their ability to perform, daily functional activities, and overall quality of life will be evaluated before treatment begins, immediately after treatment, and at a 3 month follow up.
Interventions
BEHAVIORALcognitive-behavioral therapy
In addition to standard medical care, the children and parents in the family CBT condition will also receive education about chronic pain, pain behaviors and operant strategies as well as training in coping skills using an interactive, engaging format on the Internet. The Internet site will consist of three main sections: child treatment modules, parent treatment modules, and diary tracking. All users will complete 8 treatment modules (one per week) over the 8-week treatment period. Each module will require approximately 30-40 minutes to complete. There is separate specific content of the intervention for child users and for parent users. Assignments are incorporated into each module for the participant to work on during the treatment week.
Sponsors
Seattle Children's Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
12 Years to 18 Years
Healthy volunteers
No
Inclusion criteria
* chronic headache, abdominal, and/or musculoskeletal pain present over the previous 3 months * interference from pain in at least one area of daily functioning.
Exclusion criteria
* serious comorbid chronic condition in the patient (e.g., diabetes, cancer) * non-English speaking * previous participation in cognitive-behavioral therapy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| activity limitations | immediately post-treatment, 3 month follow-up |
Secondary
| Measure | Time frame |
|---|---|
| pain intensity | immediately post-treatment, 3 month follow up |
| parental response to pain behaviors | immediately post-treatment, 3 month follow-up |
| depressive symptoms | immediately post-treatment, 3 month follow-up |
Outcome results
None listed