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impact of psychoeducational intervention on patient with inflammatory bowel disease

the investigation of Impact of psycho educational intervention on physical and psychological symptoms in patients with inflammatory bowel disease

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015041921850N1
Enrollment
60
Registered
2016-01-12
Start date
2015-08-16
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

inflammatory bowel disease. crohn disease[reginal enteritis]-ulceritive colitis

Interventions

Intervention 1: The intervention group training classes for 4 meeting will be held within one month, training include: training, diet, exercise, stress management, anxiety, depression, learning ways
The intervention group training classes for 4 meeting will be held within one month, training include: training, diet, exercise, stress management, anxiety, depression, learning ways to deal with an
The control group did not receive the intervention at the end of the training manual given to them.

Sponsors

Vice chancellor for research , Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:Willingness to participate in the study; Age over 18 years Patients diagnosed with the disease; Patients in the active phase of the disease Ability to perform physical activity; Not with other chronic illnesses Exclusion criteria: patient's lack of cooperation during the investigation

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Physicall symptom. Timepoint: before the intervention and 4 weeks and 8 weeks after intervention. Method of measurement: Crohn's Disease Activity Index,Clinical Scoring System for the CLINICAL colitis Activity Index.;Psychological intervention. Timepoint: befor the intervention,4 weeks after intervention,8 weeks after intervention. Method of measurement: HADS Questionary.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Molazem

Shiraz University of Medical Sciences

Molazemzah@yahoo.com+98 71 3647 4254

Outcome results

None listed

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