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February 2, 2026BMJ Open0 citationsOpen Access

Breathing control training as a treatment for functional seizures (BREATHS trial): a multicentre, assessor-blinded, randomised controlled efficacy and acceptability trial study protocol

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RKRichard Antony Alexander KanaanRDRod DuncanPKPeter Koval

Key Points

  • The aim is to confirm the efficacy and acceptability of breathing control training for functional seizures.
  • Conduct a 24-week multicentre, assessor-blinded, randomised controlled trial.
  • Randomly assign 220 participants with functional seizures to BCT or control (Befriending).
  • Deliver two treatment sessions over 4 weeks via a respiratory physiotherapist or telehealth.
  • Assess participants' progress at 4, 12, and 24 weeks.
  • Initial open-label pilot trial showed BCT was safe and effective in reducing seizure frequency.
  • The new trial seeks to validate these findings and assess overall acceptability.

Abstract

Introduction Functional seizures (FS) are events that resemble epileptic seizures, but are not attributed to brain pathology and are instead thought to be due to psychological factors. A small, multisite, open-label, single-arm, pilot trial of a breathing intervention known as breathing control training (BCT) found it to be safe and effective in reducing seizure frequency in FS. We propose a protocol for a study to confirm these results. Methods and analysis A 24-week, multicentre, individually-randomised, assessor-blinded, two-arm, parallel-group efficacy and acceptability trial of BCT versus control (Befriending) in 220 participants ≥16 years of age with FS. Eligible participants will be randomly allocated to receive two sessions of either BCT or Befriending over a 4-week period. Sessions will be delivered by a respiratory physiotherapist at a clinical care site or via telehealth. They will complete assessments prior to commencing treatment and at 4, 12 and 24 weeks after their initial session of BCT/Befriending. The trial will be conducted alongside treatment as usual. An economic evaluation including cost-utility and cost-effectiveness analyses will be carried out from health sector and societal perspectives. Ethics and dissemination The study has been approved by The Austin Health Human Research Ethics Committee (HREC/84335/Austin-2022) and the New Zealand Central Health and Disability Ethics Committee (2022 FULL 12324). Findings will be reported to trial participants and consumers; presented at local, national and international conferences; and disseminated by a peer-reviewed scientific journal.

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Cite This Study

Kanaan et al. (2026) studied this question.

synapsesocial.com/papers/6980ffa4c1c9540dea81245chttps://doi.org/10.1136/bmjopen-2025-107687
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