Trial Details

Not Recruiting
Basic Information
Clinical ID c2547
Identifier IRCT20200219046553N1
Trial Title Effect of mindfulness-based cognitive therapy on quality of Life , emotional symptom , dimensions of pain , dispositional mindfulness and disease activity in patients with inflammatory bowel disease
Trial URL Visit Original Page
Study Information
Study Results

No results available

Conditions Condition 1: Mindfulness-based cognitive therapy(MBCT). Condition 2: Crohn's disease. Condition 3: Ulcerative colitis. Condition 4: Depression. Condition 5: Anxiety. Crohn's disease [regional enteritis] Ulcerative colitis Major depressive disorder, single episode, mild Anxiety disorder, unspecified;F32.0;F41.9
Interventions Intervention 1: Intervention group:These people receive mindfulness-based cognitive therapy in addition to their usual medical treatment.Mindfulness-based cognitive therapy (MBCT) is an evidence-based psychological group program designed to help manage stress and depressive symptoms. MBCT is an 8-week, facilitator-led, group-based psychological intervention. In addition to the 2-h weekly group sessions, there is a guided home practice component for up to 45 min a day. Within the 8 weeks, participants practice a series of mindfulness meditation, cognitive-behavioural therapy and stretching exercises within the group and at home. During the programme, participants become more aware of their body sensations, thoughts and emotions and their interrelatedness. Intervention 2: Control group: People in the control group receive their usual medical treatment as before, and during the study period follow-up sessions are held to monitor the status of these patients (including the possibility of exacerbation of symptoms). The sessions also explain the inflammatory bowel disease and its complications, and participants discuss the symptoms they are experiencing.
Participant Information
Sponsor Kashan University of Medical Sciences
City -
Country/Region Iran
Enrollment Criteria
Sex Requirement ALL
Age Requirement ADULT
Study Design
Study Type interventional
Phase Not Available
Time Information
Start Date 2025-04-24
Primary Completion Date -
Completion Date -