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Impact of educational programs, self-hypnosis, and web-based bioenergy economics on patients with irritable bowel syndrome

Phase 3
Recruiting
Conditions
Irritable bowel syndrome.
Irritable bowel syndrome
Registration Number
IRCT20190404043159N6
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
120
Inclusion Criteria

Both male and female participants aged 18 to 65 years
Diagnosis of moderate to severe IBS based on ROME III criteria and exclusion of potential organic causes by gastroenterology specialists
Basic literacy skills (reading and writing)
Ability to work with and access software applications
Satisfaction to participate in the study

Exclusion Criteria

Diagnosis of any organic disease during the study period that renders continued participation impossible
Diagnosis of depression disorders, bipolar disorders, or psychotic disorders based on DSM-V diagnostic criterias assessed by a psychiatrist and psychiatric assistant
Serious suicidal thoughts or plans at the time of study entry
Use of antidepressant or antianxiety medications within 2 weeks prior to study entry
Participation in psychotherapeutic programs within 2 months prior to study entry
Pregnant or breastfeeding
History of bowel surgery
Substance abuse since the onset of symptoms

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of Irritable Bowel Syndrome symptoms. Timepoint: Before and after 6 weeks training. Method of measurement: The irritable bowel severity scoring system (IBSSS).;Depression. Timepoint: Before and after 6 weeks training. Method of measurement: Hospital Anxiety and Depression Scale (HADS).;Anxiety. Timepoint: Before and after 6 weeks training. Method of measurement: Hospital Anxiety and Depression Scale (HADS).;Quality of life. Timepoint: Before and after 6 weeks training. Method of measurement: Irritable Bowel Syndrome Quality of Life (IBS-QOL-34).;Awareness level. Timepoint: Before and after 6 weeks training. Method of measurement: Which number from 0 to 100 rates your awareness level of your disease?.
Secondary Outcome Measures
NameTimeMethod
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