Treatment of Rumination

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorHospital Universitari Vall d'Hebron Research Institute

About this trial

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 with daily exercises, while control participants will take a placebo with each meal. Treatment response will be assessed by comparing outcomes before and after the intervention. After post-treatment assessment, control group participants will be offered the opportunity to receive biofeedback therapy.

Relevance: This project aims to determine the efficacy of a simplified mechanistic intervention for rumination. If successful, this approach could be adopted in additional healthcare settings.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Rumination syndrome

Disqualifiers

Relevant organic diseases

Trial design

Design model

Parallel

Treatments tested in this trial

  • Biofeedback

    Behavioral

    Three sessions of biofeedback before and after a standardized meal.

  • Placebo

    Dietary supplement

    Three sessions of placebo followed by standardized meal.

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: BiofeedbackExperimental treatment 1 intervention
Group B: PlaceboPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Number of rumination events after a challenge meal measured by an event marker.

Each regurgitation event will be registered by the patient using an event marker.

Time frame
4 weeks

Secondary outcomes

1

Number of self perceived rumination events

Number of rumination events measured by questionnaires administered daily for 7 days before and at the end of treatment.

Time frame
4 weeks
2

Number of rumination events

Number of rumination events measured by questionnaires administered daily for 7 days, 1 month after treatment.

Time frame
1 month
3

Number of rumination events

Number of rumination events measured by questionnaires administered daily for 7 days, 3 months after treatment.

Time frame
3 months
4

Number of rumination events

Number of rumination events measured by questionnaires administered daily for 7 days, 6 months after treatment.

Time frame
6 months

Other outcomes

Sponsors and contacts

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