Treatment of Functional Abdominal Distension

NACompletedINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

July 25, 2019

Primary Completion Date

January 19, 2021

Study Completion Date

January 17, 2022

Conditions
Irritable Bowel SyndromeDyspepsia
Interventions
BEHAVIORAL

Biofeedback

Three sessions of biofeedback will be performed during the first 3 weeks of the intervention period. Biofeedback sessions will be performed 30 min after ingestion of the offending meal: patients will be taught to control abdominal and thoracic muscular activity by providing a visual display of the abdominal and thoracic perimeter; specifically, they will be instructed to reduce the abdominal perimeter (girth). Patients will be instructed to perform the same exercises before and after breakfast, lunch and dinner during the 4-week intervention period.

DIETARY_SUPPLEMENT

Placebo

Three sessions will be performed during the first 3 weeks of the intervention period. Each session will be performed 30 min after ingestion of the offending meal: abdominal and thoracic perimeter will be recorded but not shown to the patient; patients will take a pill of placebo containing 0.5 g glucose and no specific instructions will be provided. 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

University Hospital Vall d'Hebron, Barcelona

All Listed Sponsors
lead

Hospital Universitari Vall d'Hebron Research Institute

OTHER

NCT04043208 - Treatment of Functional Abdominal Distension | Biotech Hunter | Biotech Hunter