Actively Recruiting
Patients With Irritable Bowel Syndrome and Physiotherapy
Led by Istanbul Saglik Bilimleri University · Updated on 2024-10-02
72
Participants Needed
1
Research Sites
30 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The research will be planned on 72 individuals between the ages of 18-65 who were diagnosed with irritable bowel syndrome at Istanbul Medipol University Çamlıca SUAM Gastroenterology Polyclinic. Patients will be divided into 3 groups; High-intensity interval training and a disease-specific nutrition program for the first group, and a disease-specific nutrition program for the second group; Basic Body Awareness Therapy (BBAT) and a disease-specific nutrition program will be given, while the control group will be given only a disease-specific nutrition program. Evaluations will be made immediately before and after treatment. The first experimental group will be asked to walk with high-intensity interval training, which the investigators plan for 30 minutes, 4 days a week for 8 weeks. TBFT will be applied to the second experimental group every day of the week. The application will be done face to face one day a week, and the patient will be asked to do it himself on the other days, and the sessions will last approximately 30 minutes. In addition, all patients will be asked to follow the nutrition program determined by the dietician. Participants' sociodemographic information, IBS disease type and medications used will be recorded. In order to collect data for both the intervention groups and the control group immediately before and after the study; 6 Minute Walk Test (6MWT), posture analysis, muscle shortness test for large muscle groups in the lower and upper extremities, International Physical Activity Questionnaire Short Form (IPAQ-SF), Diet Compliance Questionnaire Form, Bristol Stool Scale Form, Gastrointestinal Symptom Assessment Scale (GSDS). ), Pittsburgh Sleep Quality Index (PSQI), IBS Quality of Life Scale (IBS-QOL), Morningness-Eveningness Questionnaire (SAA), Psychological Well-Being Scale (PIOS) and Body Awareness Questionnaire (VFA) will be used.
CONDITIONS
Official Title
Patients With Irritable Bowel Syndrome and Physiotherapy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be between 18 and 65 years old
- Meet Rome IV criteria for irritable bowel syndrome
- Willing to participate and provide written consent
You will not qualify if you...
- Voluntary refusal to participate
- Have a psychiatric illness
- Have orthopedic, neurological, or cardiopulmonary diseases that contraindicate the study protocols
- Pose a risk of injury based on posture analysis
- Have muscle shortness limiting participation
- Regular use of laxatives
- Diagnosis of diabetes or metabolic diseases affecting the gastrointestinal system
- History of inflammatory bowel disease, colon cancer, or colon resection
- Use of antibiotics or probiotics within the last 3 months
- Use of anticholinergic, opiate, or morphine-type drugs affecting intestinal motility
- Diagnosis of celiac disease
AI-Screening
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Trial Site Locations
Total: 1 location
1
Medipol Camlica Suam Hospital
Istanbul, Turkey (Türkiye)
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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