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Functional and Respiratory Rehabilitation and Nutritional Care of COVID-19 Patients (RECOVER-19)

Functional and Respiratory Rehabilitation and Nutritional Care of COVID-19 Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04466800
Acronym
RECOVER-19
Enrollment
160
Registered
2020-07-10
Start date
2020-07-30
Completion date
2023-01-13
Last updated
2023-01-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID

Keywords

COVID, Rehabilitation, Adapted physical activity, Malnutrition

Brief summary

Following the acute phase of COVID, some patients may have sequelae, such as breathing difficulties or malnutrition. We hypothesize that a functional and respiratory rehabilitation program associated with personalized nutritional care will improve quality of life, physical performance and respiratory capacities and will decrease the prevalence of malnutrition among those patients.

Detailed description

In France, more than 150 000 patients have been infected by the SARS-CoV-2 virus and COVID has been responsible for more than 100 000 hospitalizations. Following the acute phase of this disease, some patients may have sequelae, such as breathing difficulties or malnutrition. However, the prevalence and intensity of those sequelae still remain unknown. Thus, a functional and respiratory rehabilitation program associated with personalized nutritional care may be necessary to improve those patients' prognosis. This study aims to evaluate the effectiveness of a 4-week rehabilitation program following the acute phase of COVID. This program includes regular physical activity supervised by a physical acticity educator, a systematic malnutrition screening and a nutritional follow-up performed by a dietitian. Patients will be randomized in two groups: rehabilitation program (intervention group) or usual care (control group). Quality of life, physical performance, respiratory capacities and nutritional status will be assessed in both groups at inclusion and one month later (corresponding to the end of the rehabilitation program for the intervention group).

Interventions

OTHERIntervention group_rehabilitation program

Regular physical activity, supervised by a physical education educator, a systematic malnutrition screening and a nutritional follow-up performed by a dietetician. Patients will follow a 4-week rehabilitation program, comprising 3 physical activity sessions per week for 4 weeks. First sessions will be supervised by a physical activity educator and patients will perform the following sessions at home, using physical training software. The physical activity educator will call patients once a week to ensure the sessions are correctly performed and adapt the program if necessary. Patients will also undergo a nutritional assessment carried out by a dietitian at the beginning of the program. A dietitian will call patients once a week to ensure their nutritional status is appropriate.

Sponsors

Rennes University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Multicenter, randomized, comparative, parallel-group trial

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age above 18 years * Laboratory (RT-PCR and/or serology) confirmed infection with SARS-CoV-2 * Date of first symptoms of SARS-CoV-2 infection \> 4 weeks and \< 4 months * Persisting functional and/or respiratory deficit and/or asthenia and/or malnutrition beyond the first 4 weeks after COVID, defined as : * Increase of mMRC (Modified Medical Research Council) score ≥ 1 between the month before COVID and beyond the first 4 weeks after COVID and/or * Asthenia score (Pichot asthenia scale) \> 22 beyond the first 4 weeks after COVID, if patient had no asthenia before COVID (asthenia score \<8) and/or * Weight loss \> 5% within 6 months, comparing minimum weight between the month before COVID and beyond the first 4 weeks after COVID and/or * BMI (Body Mass Index) \< 20 (if age \< 70 years) or \< 22 (if age ≥ 70 years) if BMI (Body Mass Index) ≥ 20 (if age \< 70 years) or ≥ 22 (if age ≥ 70 years) the month before COVID * Patient affiliated to social security system * Patient gave written informed consent

Exclusion criteria

* Patient unable to undergo a rehabilitation program due to comorbidities, such as major cardio-vascular disease or severe dementia * Patient currently benefiting from physiotherapy sessions, in particular motor and / or respiratory therapy and / or an exercise re-training and / or respiratory rehabilitation program * Patient living in a residential facility for dependent elderly people * Patient not speaking french * Pregnant women

Design outcomes

Primary

MeasureTime frameDescription
Impact of a multidisciplinary and personalized rehabilitation program on COVID patients's quality of life1 monthPhysical component score of the Short-Form 36 health survey between the beginning and the end of the rehabilitation program (from 0 to 100; highers scores mean better outcome)

Secondary

MeasureTime frameDescription
Impact of a multidisciplinary and personalized rehabilitation program in terms of Respiratory capacities1 monthModified Medical Research Council scale (mMRC) (from 0 to 4, highers scores mean worse outcome)
Impact of a multidisciplinary and personalized rehabilitation program in terms of Functional capacities1 monthBarthel scale (from 0 to 100, highers scores mean worse outcome)
Impact of a multidisciplinary and personalized rehabilitation program in terms of Malnutrition prevalence rate using GLIM malnutrition diagnostic criteria1 monthWeight loss
Impact of a multidisciplinary and personalized rehabilitation program in terms of mortality1 monthMortality rate
Impact of a multidisciplinary and personalized rehabilitation program in terms of Physical capacities1 monthNumber of repeated chair rises during 3 minutes
Impact of a multidisciplinary and personalized rehabilitation program in terms of Anxiety and depression1 monthHospital and Anxiety Depression Scale (from 0 to 42, highers scores mean worse outcome)
Impact of a multidisciplinary and personalized rehabilitation program in terms of Healthcare consumption1 monthNumber of consultations with the healthcare professionals
Impact of a multidisciplinary and personalized rehabilitation program in terms of Medico-economic evaluation3 monthsIncremental cost-effectiveness ratio
Patient's opinion concerning the rehabilitation program3 monthsSatisfaction questionnaire with open-ended questions (no specific scale is available)
Impact of a multidisciplinary and personalized rehabilitation program in terms of Quality of life1 monthScore of the Short-Form 36 health Survey (from 0 to 100, highers scores mean better outcome)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026