The Efficacy Of The Unified Transdiagnostic Treatment for Irritable Bowel Syndrome
Not Applicable
- Conditions
- Irritable bowel syndrome.irritable colon
- Registration Number
- IRCT2017010431765N1
- Lead Sponsor
- Vice chancellor for research of Kashan University of Medical Sciences and Health Services
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 64
Inclusion Criteria
diagnosis IBS based on the criteria of Rome III; aged between 18 and 40 years; satisfaction and commitment to participate in the study
Exclusion criteria: get interventions psychological treatment in the past year and the time of the study; history of alcohol abuse or drugs; two sessions of absence for each patient.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Depression. Timepoint: Before intervention, After intervention, One month after intervention. Method of measurement: subscale depression dass-42.;Anxiety. Timepoint: Before intervention, After intervention, One month after intervention. Method of measurement: subscale anxiety dass-42.;Stress. Timepoint: Before intervention, After intervention, One month after intervention. Method of measurement: subscale stress dass-42.;Emotion regulation. Timepoint: Before intervention, After intervention, One month after intervention. Method of measurement: emotion regulation questionnaire.;Severity of symptoms in patients with irritable bowel syndrome. Timepoint: Before intervention, After intervention, One month after intervention. Method of measurement: IBS Symptom Severity Scoring.
- Secondary Outcome Measures
Name Time Method