Treatment of Functional Abdominal Distension by Non-instrumental Biofeedback

NAActive, not recruitingINTERVENTIONAL
Enrollment

41

Participants

Timeline

Start Date

April 29, 2024

Primary Completion Date

December 8, 2024

Study Completion Date

July 14, 2025

Conditions
Irritable Bowel SyndromeDyspepsiaFunctional Bloating
Interventions
BEHAVIORAL

Biofeedback

Three sessions of biofeedback intervention will be performed during the first 3 weeks of the intervention period. Patients will be taught to control abdominal and thoracic muscular activity by providing instructions using an original video support. Patients will be instructed to perform the same exercises before and after breakfast, lunch and dinner during the 4-week intervention period.

BEHAVIORAL

Placebo

Three sessions of placebo intervention will be performed during the first 3 weeks of the intervention period. Sham measurements of abdominal and thoracic motion will be performed, and a pill of placebo containing 0.21 g glucose will be administered; patients will be instructed to take a pill of placebo before breakfast, lunch and dinner during the 4-week intervention period.

Trial Locations (1)

08035

Hospital Universitari Vall d'Hebron, Barcelona

All Listed Sponsors
lead

Hospital Universitari Vall d'Hebron Research Institute

OTHER

NCT06150638 - Treatment of Functional Abdominal Distension by Non-instrumental Biofeedback | Biotech Hunter | Biotech Hunter