Skip to content

The effect of Positive Thinking Interventions in irritable bowel syndrome

The effect of Positive Thinking Interventions on severity of symptoms and pain catastrophizing in irritable bowel syndrome patients: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250802066728N1
Enrollment
56
Registered
2025-08-12
Start date
2025-09-06
Completion date
Unknown
Last updated
2025-08-19

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

Conditions

Irritable bowel syndrome. Irritable bowel syndrome

Interventions

Intervention 1: Intervention group: In this study, the positive thinking intervention consists of an 8-week virtual training program. The program includes eight pre-recorded audio sessions (podcasts),
cultivating strengths
strength identification exercise, Performing acts of kindness
forgiveness practice
forg

Sponsors

Birjand University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Diagnosis of IBS based on ROME IV criteria by a gastroenterologist Ability to read and write Age 18-65 years Not suffering from acute psychiatric disorders (schizophrenia) and use psychoactive drugs for at least three months Not participating in similar training courses in the last 3 months No use of complementary medicine treatments one month before and during the treatment

Exclusion criteria

Exclusion criteria: Unwillingness to continue participating in the study Absence in more than 2 sessions of the intervention process (not providing feedback, not completing assigned homework, and not listening to podcasts) Diagnosis of other structural or functional gastrointestinal diseases during the study period Appearance of new and severe gastrointestinal symptoms such as gastrointestinal bleeding during the study period Use of psychotropic medications and diagnosis of acute psychiatric disorders during the study period

Design outcomes

Primary

MeasureTime frame
Severity of gastrointestinal symptoms. Timepoint: At baseline and immediately after the intervention (week 8). Method of measurement: Gastrointestinal Symptom Rating Scale by Revicki et al. (1998).;Pain catastrophizing. Timepoint: At baseline and immediately after the intervention (week 8). Method of measurement: Pain catastrophizing Scale by Sullivan et al. (1995).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbolfazl Vagharseyyedin

Birjand University of Medical Sciences

waghars@yahoo.com+98 56 3239 5000

Outcome results

None listed

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