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

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

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.