Treament of Rumination

NACompletedINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

December 2, 2019

Primary Completion Date

October 30, 2020

Study Completion Date

February 1, 2022

Conditions
Rumination Disorders
Interventions
BEHAVIORAL

Biofeedback

Three sessions by biofeedback will be performed during the first 3 weeks of the intervention period. In each session patients will be taught to control abdominal and thoracic muscular activity by providing a visual display of the abdominal and thoracic perimeter; 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. In each session 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

Vall d'Hebron Research Institute, Barcelona

All Listed Sponsors
lead

Hospital Universitari Vall d'Hebron Research Institute

OTHER

NCT04167371 - Treament of Rumination | Biotech Hunter | Biotech Hunter