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effective of mindfulness and ACT on inflammatory bowel disease

Comparing the Effectiveness of Mindfulness Based Stress Reduction and Acceptance and Commitment Therapy on Physiological and Psychological Symptoms in Inflammatory Bowel Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190708044156N1
Enrollment
160
Registered
2020-12-23
Start date
2019-06-21
Completion date
Unknown
Last updated
2021-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammatory bowel disease. Ulcerative colitis

Interventions

Intervention 1: first Intervention group called "Acceptance and commitment therapy": it includes 8 psychological training sessions in 1.5 hours. each session is included one of these subjects: ACT int

Sponsors

Kerman University of Medical Sciences,Deputy of Research, Gastroenterology Research Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: inflammatory bowel disease patients who have inactive and under control disease

Exclusion criteria

Exclusion criteria: Patients under 18 years Patients over 65 years pregnant females patients currently attending psychiatric services patients currently receiving antidepressant medication patients who have received steroid medications in the past three months patients who have previously undergone a stress management programme (relaxation techniques, psycho dynamic psychotherapy, cognitive behavioral therapy, hypnosis)

Design outcomes

Primary

MeasureTime frame
Colitis physiological symptoms. Timepoint: before intervention, after intervention and 60 days after intervention. Method of measurement: Partial Mayo Scoring Index Assessment.;Stress. Timepoint: before intervention, after intervention and 60 days after intervention. Method of measurement: Depression, Anxiety and Stress Scale questionnaire (DASS-21).;Anxiety. Timepoint: before intervention, after intervention and 60 days after intervention. Method of measurement: Depression, Anxiety and Stress Scale questionnaire (DASS-21).;Depression. Timepoint: before intervention, after intervention and 60 days after intervention. Method of measurement: Depression, Anxiety and Stress Scale questionnaire (DASS-21).;Quality of life. Timepoint: before intervention, after intervention and 60 days after intervention. Method of measurement: world health quality of life questionnaire (BREF form).;General Health. Timepoint: before intervention, after intervention and 60 days after intervention. Method of measurement: general health questionnaire (GHQ-28).;Pain perception. Timepoint: before intervention, after intervention and 60 days after intervention. Method of measurement: Mcgill pain perception questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFateme Sheikh-ali Saghaie

Bahonar University of Kerman, Iran

fateme.saghaie@gmail.com+98 34 3281 9168

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026