Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Cardiac-coherence breathing training for adults with Long COVID in Réunion

Official title: Randomized Controlled Trial Evaluating the Effectiveness of a Breathing Control Technique on Long COVID Symptoms at the Reunion University Hospital

Run by Centre Hospitalier Universitaire de la Réunion · NCT05851859 · Data updated 2026-11-12

This project will test whether a simple breathing-control method (cardiac coherence) helps adults in Réunion with Long COVID reduce symptoms and improve daily functioning.

More Long COVID trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment200 (estimated)
SponsorCentre Hospitalier Universitaire de la Réunion
Academic / other
Locations2 sites (Saint-Denis and 1 other locations)
StatusRecruiting
StartedMay 5, 2025
Main results expectedNovember 2026
Study endsApril 2027
Registry record updatedSeptember 14, 2026
Trial IDNCT05851859 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) living in Réunion with a WHO‑defined diagnosis of Long COVID and a documented prior SARS‑CoV‑2 infection who test antigen‑negative at inclusion are ideal candidates.

Probably not a fit

Patients with chronic or disabling respiratory disease that prevents respiratory training, those already practicing similar breathing techniques within the last six months, or people taking excluded cardiac or psychoactive medications are unlikely to benefit from this program.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Adults living in Réunion who meet the WHO definition of Long COVID and can document prior SARS‑CoV‑2 infection with a negative antigen test will be enrolled at CHU de la Réunion (Saint‑Denis and Saint‑Pierre). Participants will receive structured training in a cardiac coherence breathing technique (guided slow breathing to improve heart‑rate variability) as the interventional program. Symptom scores and functional outcomes will be recorded over time to measure change after the breathing program, with predefined exclusions for respiratory comorbidity, recent breathing‑technique practice, certain cardiac medications or devices, pregnancy, cognitive impairment, or guardianship. The intervention is non‑pharmacologic and delivered in an outpatient hospital setting.

Why it matters

Potential benefit: If effective, the breathing technique could reduce symptom burden and improve daily functioning and quality of life for people with Long COVID.

How similar studies have gone: Breathing‑retraining and heart‑rate‑variability techniques have shown some symptom and quality‑of‑life improvements in other post‑viral and long‑COVID cohorts, but results across studies are limited and mixed.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients over the age of 18,
* living in Reunion and
* having a diagnosis of Long COVID according to the World Health Organization (WHO) definition will be included in this study.
* These patients must attest to their primary infection with Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) and present a negative antigen test at the time of inclusion.

Exclusion Criteria:

Patients:

* with a chronic or disabling respiratory pathology preventing respiratory training (asthma, Chronic Obstructive Pulmonary Disease (COPD), active tuberculosis, pulmonary sequelae of COVID-19, etc.) practicing or having practiced a regular respiratory control technique (yoga, Cardiac coherence training, etc.) in the last 6 months
* taking a beta-blocker, betamimetic, anti-arrhythmic, morphine, antidepressant treatment (Escitalopram)
* having a pacemaker or severe heart disease
* Current and known pregnancy or breastfeeding woman
* with a cognitive deficit
* under guardianship/curators or under judicial protection

Where it's running

  • CHU de la Réunion
    Saint-Denis, France
    Recruiting
  • CHU de la Réunion
    Saint-Pierre, France
    Not yet recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.