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Study identifier: NCT06971354 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Treatment of Rumination

Condition: Rumination Syndrome  ·  Sponsor: Hospital Universitari Vall d'Hebron Research Institute

PhaseNA
Planned participants40
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

Background: Rumination syndrome is characterized by the involuntary regurgitation of previously ingested food from the stomach to the mouth, triggered by an unintentional contraction of the abdominal muscles along with simultaneous relaxation of the esophageal sphincters. Based on this mechanism, a biofeedback technique targeting muscular activity has been developed and shown to be effective. However, such techniques are often complex and not widely accessible. Hypothesis: Rumination can be effectively treated using a simplified, non-instrumental biofeedback technique based on cognitive intervention. Objective: To evaluate the effectiveness of a non-instrumental biofeedback technique incorporating cognitive intervention for the treatment of rumination. The methodology will build on prior studies, employing a more streamlined biofeedback approach. Methods: Participants will be assigned to parallel groups with balanced sex distribution. The study will compare responses to biofeedback versus a control intervention. Over a four-week period, each participant will undergo three treatment sessions: The biofeedback group will be trained to control abdominothoracic musculature through cognitive intervention, supported by original visual materials, both before and after a standardized test meal. The control group will receive a placebo capsule prior to the test meal, and regurgitation episodes will be recorded. Following the initial session, biofeedback participants will continue…

This description comes directly from the study's public registry record.

Talk to the study team

Jordi Serra, M.D.  ·  34 93 274 6259  ·  jordiserra@vallhebron.cat

Gloria Santaliestra  ·  34 932746259  ·  gloria.santaliestra@vhir.org

Always discuss trial participation with your own doctor first.

Locations (1)

Vall d'Hebron Research InstituteBarcelona, SpainRecruiting

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Source record: clinicaltrials.gov/study/NCT06971354