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Clinical Trials/NCT06596759
NCT06596759RecruitingNot Applicable

Diaphragmatic Breathing for the Treatment of Bloating and Distension: a Prospective Pilot Study

Mayo Clinic2 sites in 1 country35 target enrollmentStarted: October 21, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
35
Locations
2
Primary Endpoint
Change in Mayo Bloating Questionnaire (MBQ) score

Study Overview

Brief Summary

The purpose of this study is to evaluate the efficacy of diaphragmatic breathing using the validated Mayo Bloating Questionnaire.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Referred for breath testing for the indication of bloating.

Exclusion Criteria

  • Not referred for breath testing for the indication of bloating.

Arms & Interventions

Diaphragmatic Breathing

Experimental

Patients will complete the Mayo Bloating Questionnaire (MBQ) before referral to a physical therapist for in diaphragmatic breathing (DB) techniques over a 30-minute session. The patient will be instructed to complete 5-10 minutes of diaphragmatic breathing twice a day for a period of 4 weeks. At the end of the 4-week follow up period, patients will repeat the MBQ and self-report their adherence to daily diaphragmatic breathing.

Intervention: Diaphragmatic Breathing (Behavioral)

Outcomes

Primary Outcomes

Change in Mayo Bloating Questionnaire (MBQ) score

Time Frame: Baseline, 4 weeks

The Mayo Bloating Questionnaire is a 45-item questionnaire developed to measure the multiple symptom components of bloating and distension.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Brian Lacy

Principal Investigator

Mayo Clinic

Study Sites (2)

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