Alternate Nostril Breathing (ANB) for 1st Trimester Nausea and Vomiting

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversity of Minnesota

About this trial

This is a prospective, two-arm, non-blinded randomized controlled study designed to evaluate the effects of a one-week alternate nostril breathing (ANB) intervention on nausea and vomiting severity in pregnant individuals during their first trimester.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Pregnant individuals aged 18 years or older

Viable pregnancy with a gestational age between 6 0/7 - 12 6/7 weeks of gestation, confirmed by last menstrual period or ultrasound

Diagnosed with mild to moderate NVP (PUQE-24 score between 4-12)

Ability to understand and read English

Disqualifiers

Severe nausea and vomiting, defined as a PUQE score >12, or diagnosis of hyperemesis gravidarum requiring hospitalization or intravenous fluid therapy

Pre-existing, active or acute respiratory conditions (e.g., asthma, COPD)

History of severe anxiety disorders affecting breathing patterns

Known deviated nasal septum

Trial design

Design model

Parallel

Treatments tested in this trial

  • Alternate Nostril Breathing

    Behavioral

    ANB 3 times per day for 5-10 minutes per session over a 7-day period

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Alternate Nostril BreathingActive comparator 1 intervention
Group B: Usual Care OnlyNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Severity of Nausea and Vomiting

Measured by the change in the Pregnancy-Unique Quantification of Emesis and Nausea (PUQE) score, where scores range from 3-15, and a higher score indicates greater severity of nausea and vomiting.

Time frame
Day 7

Secondary outcomes

Other outcomes

Sponsors and contacts

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