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Sponsors and Collaborators: |
Children's Mercy Hospital Kansas City University of Arizona |
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Information provided by: | Children's Mercy Hospital Kansas City |
ClinicalTrials.gov Identifier: | NCT00327548 |
The purpose of the study is to evaluate the effectiveness of relaxation, with or without guided imagery, for treating children with functional abdominal pain. The study will evaluate a child's ability to decrease the amount of pain with these techniques to allow continuation of normal daily activities at home and at school. The hypothesis is that these relaxation techniques will help decrease reports of abdominal pain and improve levels of activity.
Condition | Intervention | Phase |
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Functional Abdominal Pain |
Behavioral: guided imagery |
Phase III |
Study Type: | Interventional |
Study Design: | Randomized, Double-Blind, Placebo Control, Parallel Assignment |
Official Title: | Treatment of Functional Abdominal Pain in Children:Evaluation of Relaxation/Guided Imagery and Chamomile Tea as Therapeutic Modalities |
Ages Eligible for Study: | 5 Years to 18 Years |
Genders Eligible for Study: | Both |
Inclusion Criteria:
at least 3 episodes of abdominal pain over the previous 3 months normal complete blood count, sedimentation rate, urinalysis stable on current medications English speaking -
Exclusion Criteria:
unwillingness to participate chronic gastrointestinal disease cognitive-developmental delay major dissociative disorder
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Study ID Numbers: | NIH 5P50-AT00008 |
Study First Received: | May 16, 2006 |
Last Updated: | October 4, 2006 |
ClinicalTrials.gov Identifier: | NCT00327548 |
Health Authority: | United States: Institutional Review Board |
Signs and Symptoms Signs and Symptoms, Digestive Abdominal Pain Pain |