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NCT00327548 Clinical Trial

Use of Guided Imagery for Functional Abdominal Pain in Children:

Functional Abdominal Pain Clinical Trial

Official title:
Treatment of Functional Abdominal Pain in Children:Evaluation of Relaxation/Guided Imagery and Chamomile Tea as Therapeutic Modalities

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00327548
Other study ID # NIH 5P50-AT00008
Secondary ID
Status Completed
Phase Phase 3
First received May 16, 2006
Last updated October 4, 2006

Study information
Verified date July 2002
Source Children's Mercy Hospital Kansas City
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 5 Years to 18 Years
Eligibility 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

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind

Related Conditions & MeSH terms

Intervention

Behavioral:
• guided imagery

Locations
Country Name City State
n/a

Sponsors (2)
Lead Sponsor Collaborator
Children's Mercy Hospital Kansas City University of Arizona

Outcome
Type Measure Description Time frame Safety issue
Primary Level of pain
Primary number of days of pain
Primary missed activities
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