Diaphragmatic Breathing for the Treatment of Bloating and Distension

ConditionBloating
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMayo Clinic

About this trial

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

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Referred for breath testing for the indication of bloating.

Disqualifiers

Not referred for breath testing for the indication of bloating.

Trial design

Design model

Single group

Treatments tested in this trial

  • Diaphragmatic Breathing

    Behavioral

    REDCap will be used to administer the Mayo Bloating Questionnaire (MBQ) and collect self-reported compliance to diaphragmatic breathing (DB) exercises over a 4 week follow up period. After completion of the MBQ, the patient will be taught DB techniques by an individual physical therapist face to face 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. Patients will receive a telephone call and electronic health record portal message to check progress and answer any questions. At the end of the 4-week follow up period, patients will repeat the MBQ and self-report their adherence to daily diaphragmatic breathing. The questionnaire will include prompts investigating perceived side effects and attitudes towards therapy, willingness to perform DB therapy, likelihood to attempt self-guided DB in the future, and if the participant would recommend the therapy to a friend.

Treatment groups

35 Participants
are divided into 1 treatment group
Group A: Diaphragmatic BreathingExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change in Mayo Bloating Questionnaire (MBQ) score

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

Time frame
Baseline, 4 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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