Nursing Management of Irritable Bowel Syndrome:Improving Outcomes
Irritable Bowel Syndrome
About this trial
This is an interventional treatment trial for Irritable Bowel Syndrome focused on measuring Irritable Bowel Syndrome, Cognitive-behavioral intervention, Psychological distress, Quality of life
Eligibility Criteria
Inclusion Criteria: Irritable Bowel Syndrome Exclusion Criteria: GI pathology (organic disease) Co-morbid pain disorders
Sites / Locations
- Northgate Executive 1
- University of Washington
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
No Intervention
1
2
3
Face-to-Face Individualized Comprehensive Self-Management (CSM-FF) Group. Participants in the individualized CSM-FF group will be scheduled for 9 weekly sessions with the nurse therapist followed by post-intervention follow-up assessment.
Telephone Individualized Comprehensive Self-Management (CSM-TEL) Group. Participants in the individualized CSM-FTF group will initially have 2 face-to-face meetings with the nurse therapist, 6 sessions over the phone and the final session face-to-face at 9 weeks.
Usual Care Control Group (UC). Following randomization the participants in the control group will receive two short phone calls to maintain contact during the comparable 9-week intervention in the treatment groups.