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.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | Centre Hospitalier Universitaire de la Réunion Academic / other |
| Locations | 2 sites (Saint-Denis and 1 other locations) |
| Status | Recruiting |
| Started | May 5, 2025 |
| Main results expected | November 2026 |
| Study ends | April 2027 |
| Registry record updated | September 14, 2026 |
| Trial ID | NCT05851859 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
- Study coordinator: Léa BRUNEAU
- Email: lea.bruneau@chu-reunion.fr
- Phone: 02 62 90 68 83
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Whole-body Cryotherapy for Fatigue in ME/CFS, Fibromyalgia, Long COVID
This study tests whether brief, repeated exposure to extreme cold can help reduce fatigue and related symptoms in adults with ME/CFS, fibromyalgia, or Long COVID compared to healthy controls.
-
Fatigue Investigation Using Digital Outcomes
This study tests whether digital monitoring with a smartphone app and wearables can track fatigue in people with MS or long COVID, compared with healthy volunteers.
-
Biomarker study to understand Long COVID using VIPER
This study tests biomarkers in people with Long COVID and those who recovered from COVID-19 to see how they can diagnose and track the condition over time.
-
PERCEIVE-Outreach: A scalable care model to help people with Long COVID manage heart and lung symptoms
This study tests a remote care model to see if a personalized, telehealth-based exercise program helps adults with Long COVID feel better and move more.
-
Testing PNMR plus standard care for long COVID
We’re trying PNMR along with standard care to see if it helps people with long COVID better than standard care alone.
-
Combination therapy for Long COVID symptoms using valacyclovir, celecoxib, and Paxlovid
This study tests whether a three-drug combination can reduce Long COVID symptoms in adults compared with a placebo.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.