The efficacy and feasibility study of the Group Cognitive Behavioral Therapy program for Irritable Bowel Syndrome:open label pilot study
- Conditions
- Irritable bowel syndrome
- Registration Number
- JPRN-UMIN000028702
- Lead Sponsor
- Kyoto University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 15
Not provided
1.Person in whom organic disease is suggested by the presence of warning symptoms** 2.Those who can not understand Japanese 3.Persons suffering from sever anxiety disorders and depression or with suicidal ideation (diagnose by PHQ-9) 4.Any other person whom the principal investigator has determined to be unsuitable as a participant of the study **Warning symptoms list 1.Symptoms which first appeared after 50 years of age 2.Any rectal bleeding that has not undergone sufficient medical investigation (excluding that caused by known hemorrhoids) 3.Diarrhea predominant IBS in which no colonoscopy investigation has been conducted 4.Unexplained weight loss without a change in eating habits 5.Nocturnal symptoms sufficient to cause insomnia 6.The presence of warning symptoms (anemia, inflammatory reactions or fecal occult blood) 7.A medical history that makes evaluation of this study difficult. (Past and present) 8.Persons with a family history of colon cancer in a first or second degree relative (grandparents, parents, siblings or children)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method