Efficacy and cost-effectiveness of Internet-delivered psychotherapy for irritable bowel syndrome: a randomized controlled trial comparison.
- Conditions
- irritable bowel syndrome
- Registration Number
- JPRN-UMIN000052457
- Lead Sponsor
- agoya City University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 132
Not provided
(i) At the time of enrolment, those who have received structured psychotherapy for IBS within the last two years, or are receiving it at that time, or plan to receive it during the period of participation. (ii) At the time of enrolment, are currently participating in another IBS clinical trial, or are scheduled to receive such treatment during the period of participation. (iii) Those who are currently undergoing psychiatric or psychosomatic treatment and whose attending physician has judged them to be unsuitable for participation in this study. (iv) Those who are pregnant. (v) Persons who have undergone or are currently undergoing treatment for organic diseases that may cause symptoms such as abdominal pain. (vi) Any other person who is judged to be unsuitable as a subject for this study by the principal investigator or research assistant.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method the IBS Symptom Severity Score the IBS Quality of Life Measure
- Secondary Outcome Measures
Name Time Method The visceral sensitivity index The Hospital Anxiety and Depression Scale EuroQol 5 dimensions 5-level Work Productivity and Activity Impairment Questionnaire: General Health Credibility / Expectancy Questionnaire Irritable Bowel Syndrome-Global Improvement Scale Customer Satisfaction Scale-3 adverse event or Serious adverse events