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Use of Guided Imagery for Functional Abdominal Pain in Children:

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00327548
First Posted: May 18, 2006
Last Update Posted: October 5, 2006
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
University of Arizona
Information provided by:
Children's Mercy Hospital Kansas City
  Purpose
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
Functional Abdominal Pain Behavioral: guided imagery Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double
Official Title: Treatment of Functional Abdominal Pain in Children:Evaluation of Relaxation/Guided Imagery and Chamomile Tea as Therapeutic Modalities

Resource links provided by NLM:


Further study details as provided by Children's Mercy Hospital Kansas City:

Primary Outcome Measures:
  • Level of pain
  • number of days of pain
  • missed activities

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   5 Years to 18 Years   (Child, Adult)
Sexes Eligible for Study:   All
Criteria

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

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00327548


Sponsors and Collaborators
Children's Mercy Hospital Kansas City
University of Arizona
Investigators
Study Chair: Fayez K Ghishan, MD University of Arizona
  More Information

ClinicalTrials.gov Identifier: NCT00327548     History of Changes
Other Study ID Numbers: NIH 5P50-AT00008
First Submitted: May 16, 2006
First Posted: May 18, 2006
Last Update Posted: October 5, 2006
Last Verified: July 2002

Additional relevant MeSH terms:
Abdominal Pain
Pain
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms
Signs and Symptoms, Digestive