Trial Details

Recruiting
Basic Information
Clinical ID c2404
Identifier IRCT20210306050603N1
Trial Title The effect of acupressure on anxiety, pain and quality of life in patients with inflammatory bowel disease
Trial URL Visit Original Page
Study Information
Study Results

No results available

Conditions Condition 1: bowel syndrome disease(Ulcerative colitis). Condition 2: bowel syndrome disease(Crohn's disease). Ulcerative colitis Crohn's disease [regional enteritis]
Interventions Intervention 1: Intervention group: pressure is applied at the pressure points determined in the study. After teaching these points and how to do it by the researcher in person, it is recommended that the intervention be performed three times a day for four weeks. During these four weeks, the researcher monitors the intervention daily by phone. Anxiety, pain and quality of life questionnaires are completed by the patient before the intervention and four weeks after the intervention. The pressure points are selected from st, kid, sp, and li4 pressure points according to the opinion of the acupressure specialist. Intervention 2: Control group: Touching is performed at the pressure points specified in the study. The training is performed by the researcher in person. Touch the pressure points three times a day for four weeks. The researcher monitors the intervention daily by telephone. The patient completes the Anxiety, Pain and Quality of Life questionnaires before the intervention and four weeks after the intervention. The pressure points are selected from st, kid, sp, and li4 pressure points according to the opinion of the acupressure specialist.
Participant Information
Sponsor Artesh 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 -