Evaluation of the Effectiveness of Breathing Control Technique on Long COVID Symptoms at the Reunion University Hospital

ConditionLong COVID
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire de la Réunion

About this trial

Despite the controversy, on October 6, 2021, the World Health Organization (WHO) recognized Long Coronavirus disease (COVID) by officially defining it: " symptoms appeared 3 months after the onset of the primary infection by the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2), persisting for at least 2 months and which cannot be explained by any other condition ". Long COVID can affects any type of patient and has polymorphic and fluctuating symptoms over time.

The Reunion Island is a French overseas department located in the Indian Ocean accounting more than 860,000 inhabitants. It has recorded since March 11, 2020, nearly 491,825 cases of COVID-19 and 961 deaths of hospitalized patients. Reunion's population is multi-ethnic and younger than the metropolitan France's one. It also has a higher prevalence of obesity and type 2 diabetes, two serious form factors of COVID-19. This specific context makes this island a particular study site for Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) and Long COVID.

In addition, some studies have confirmed the involvement of the autonomic nervous system (ANS) in the symptomatology of Long COVID and demonstrated that patients with a Long COVID present a dysfunction of their ANS which is objectified by a reduced Heart Rate Variability (HRV). The regulation of heart rate by the ANS is strongly favored by respiration. A regular slow and deep breathing training helps to adjust the baroreflex, which connect heart rate, breathing and blood pressure. The result of this training is an induced state called "cardiac coherence" (CC).

The investigator therefore hypothesize that respiratory training to CC could "re-educate" the ANS and durably improve the symptomatology of patients with Long COVID.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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

Trial design

Design model

Parallel

Treatments tested in this trial

  • Cardiac coherence

    Other intervention

    Use of Cardiac coherence (complementary respiratory training) during 6 month

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: Complementary respiratory training to cardiac coherence (CC)Experimental treatment 1 intervention
Group B: Usual care procedure in the event of Long COVIDNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Evaluation of the effectiveness of a respiratory training to cardiac coherence on the reduction in the symptomatology of patients with Long COVID.

mean score on the Long COVID Symptom Tool (ST) scale Score 0 to 53 / Higher score mean worse outcome

Time frame
6 months

Secondary outcomes

1

Evaluation of the effectiveness of a respiratory training to cardiac coherence on the decrease of overall symptoms over time

Long COVID Symptom Tool (ST) scale Score 0 to 53 / Higher score mean worse outcome

Time frame
T0, 1 month, 2 months, 3 months, 6 months
2

Evaluation of the effectiveness of a respiratory training to cardiac coherence on the decrease of specifics symptoms : fatigue

The 11-item Chalder Fatigue Scale (CFS-11) score 0 to 11 / Higher score mean worse outcome

Time frame
3 months, 6 months
3

Evaluation of the effectiveness of a respiratory training to cardiac coherence on the decrease of specifics symptoms : dyspnoea

Modified Medical Research Council (MMRC) dyspnoea scale score 0 to 5 / Higher score mean worse outcome

Time frame
3 months, 6 months
4

Evaluation of the effectiveness of a respiratory training to cardiac coherence on the decrease of specifics symptoms : Anxiety and Depression

Hospital Anxiety and Depression scale (HADS) Score 0 to 42 / Higher score mean worse outcome

Time frame
3 months, 6 months

Other outcomes

Sponsors and contacts

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