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

Sponsor
Rennes University Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04466800
Collaborator
(none)
160
5
2
33
32
1

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Intervention group_rehabilitation program
N/A

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).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
160 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Multicenter, randomized, comparative, parallel-group trialMulticenter, randomized, comparative, parallel-group trial
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Functional and Respiratory Rehabilitation and Nutritional Care of COVID-19 Patients
Actual Study Start Date :
Jul 30, 2020
Anticipated Primary Completion Date :
Nov 30, 2022
Anticipated Study Completion Date :
Apr 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention group_rehabilitation program

multidisciplinary and personalized rehabilitation program

Other: Intervention 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.

No Intervention: Control group

Usual care of each site, including delivery of an information sheet concerning recommended physical activity (based on WHO recommendations) and nutrition. One month after inclusion, patients of this group will be offered a rehabilitation program (as described in the intervention group, but with only one session with a physical activity educator at home) and one dietitian consultation.

Outcome Measures

Primary Outcome Measures

  1. Impact of a multidisciplinary and personalized rehabilitation program on COVID patients's quality of life [1 month]

    Physical 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 Outcome Measures

  1. Impact of a multidisciplinary and personalized rehabilitation program in terms of Physical capacities [1 month]

    Number of repeated chair rises during 3 minutes

  2. Impact of a multidisciplinary and personalized rehabilitation program in terms of Physical capacities [1 month]

    Aerobic physical capacity using Eval-DM software

  3. Impact of a multidisciplinary and personalized rehabilitation program in terms of Respiratory capacities [1 month]

    Modified Medical Research Council scale (mMRC) (from 0 to 4, highers scores mean worse outcome)

  4. Impact of a multidisciplinary and personalized rehabilitation program in terms of Respiratory capacities [3 months]

    Modified Medical Research Council scale (mMRC) (from 0 to 4, highers scores mean worse outcome)

  5. Impact of a multidisciplinary and personalized rehabilitation program in terms of Respiratory capacities [6 months]

    Modified Medical Research Council scale (mMRC) (from 0 to 4, highers scores mean worse outcome)

  6. Impact of a multidisciplinary and personalized rehabilitation program in terms of Respiratory capacities [1 month]

    Borg scale (from 0 to 10, highers scores mean worse outcome)

  7. Impact of a multidisciplinary and personalized rehabilitation program in terms of Functional capacities [1 month]

    Barthel scale (from 0 to 100, highers scores mean worse outcome)

  8. Impact of a multidisciplinary and personalized rehabilitation program in terms of Functional capacities [3 months]

    Barthel scale (from 0 to 100, highers scores mean worse outcome)

  9. Impact of a multidisciplinary and personalized rehabilitation program in terms of Functional capacities [6 months]

    Barthel scale (from 0 to 100, highers scores mean worse outcome)

  10. Impact of a multidisciplinary and personalized rehabilitation program in terms of Malnutrition prevalence rate using GLIM malnutrition diagnostic criteria [1 month]

    Weight loss

  11. Impact of a multidisciplinary and personalized rehabilitation program in terms of Malnutrition prevalence rate using GLIM malnutrition diagnostic criteria [3 months]

    Weight loss

  12. Impact of a multidisciplinary and personalized rehabilitation program in terms of Malnutrition prevalence rate using GLIM malnutrition diagnostic criteria [6 months]

    Weight loss

  13. Impact of a multidisciplinary and personalized rehabilitation program in terms of Malnutrition prevalence rate using GLIM malnutrition diagnostic criteria [1 month]

    Body mass index

  14. Impact of a multidisciplinary and personalized rehabilitation program in terms of Malnutrition prevalence rate using GLIM malnutrition diagnostic criteria [3 months]

    Body mass index

  15. Impact of a multidisciplinary and personalized rehabilitation program in terms of Malnutrition prevalence rate using GLIM malnutrition diagnostic criteria [6 months]

    Body mass index

  16. Impact of a multidisciplinary and personalized rehabilitation program in terms of Malnutrition prevalence rate using GLIM malnutrition diagnostic criteria [1 month]

    Muscular mass by brachial circumference or grip strength

  17. Impact of a multidisciplinary and personalized rehabilitation program in terms of Malnutrition prevalence rate using GLIM malnutrition diagnostic criteria [1 month]

    SEFI® score (from 0 to 10, highers scores mean better outcome)

  18. Impact of a multidisciplinary and personalized rehabilitation program in terms of Malnutrition prevalence rate using GLIM malnutrition diagnostic criteria [3 months]

    SEFI® score (from 0 to 10, highers scores mean better outcome)

  19. Impact of a multidisciplinary and personalized rehabilitation program in terms of Malnutrition prevalence rate using GLIM malnutrition diagnostic criteria [6 months]

    SEFI® score (from 0 to 10, highers scores mean better outcome)

  20. Impact of a multidisciplinary and personalized rehabilitation program in terms of mortality [1 month]

    Mortality rate

  21. Impact of a multidisciplinary and personalized rehabilitation program in terms of mortality [3 months]

    Mortality rate

  22. Impact of a multidisciplinary and personalized rehabilitation program in terms of mortality [6 months]

    Mortality rate

  23. Impact of a multidisciplinary and personalized rehabilitation program in terms of Quality of life [1 month]

    Score of the Short-Form 36 health Survey (from 0 to 100, highers scores mean better outcome)

  24. Impact of a multidisciplinary and personalized rehabilitation program in terms of Quality of life [3 months]

    Score of the Short-Form 36 health Survey (from 0 to 100, highers scores mean better outcome)

  25. Impact of a multidisciplinary and personalized rehabilitation program in terms of Quality of life [6 months]

    Score of the Short-Form 36 health Survey (from 0 to 100, highers scores mean better outcome)

  26. Impact of a multidisciplinary and personalized rehabilitation program in terms of Quality of life [1 month]

    EuroQol 5 Dimensions 5 Levels surveys (from 0 to 1, highers scores mean better outcome)

  27. Impact of a multidisciplinary and personalized rehabilitation program in terms of Quality of life [3 months]

    EuroQol 5 Dimensions 5 Levels surveys (from 0 to 1, highers scores mean better outcome)

  28. Impact of a multidisciplinary and personalized rehabilitation program in terms of Quality of life [6 months]

    EuroQol 5 Dimensions 5 Levels surveys (from 0 to 1, highers scores mean better outcome)

  29. Impact of a multidisciplinary and personalized rehabilitation program in terms of Quality of life [1 month]

    Proportion of patients returning to a professional activity

  30. Impact of a multidisciplinary and personalized rehabilitation program in terms of Quality of life [3 months]

    Proportion of patients returning to a professional activity

  31. Impact of a multidisciplinary and personalized rehabilitation program in terms of Quality of life [6 months]

    Proportion of patients returning to a professional activity

  32. Impact of a multidisciplinary and personalized rehabilitation program in terms of Anxiety and depression [1 month]

    Hospital and Anxiety Depression Scale (from 0 to 42, highers scores mean worse outcome)

  33. Impact of a multidisciplinary and personalized rehabilitation program in terms of Anxiety and depression [3 months]

    Hospital and Anxiety Depression Scale (from 0 to 42, highers scores mean worse outcome

  34. Impact of a multidisciplinary and personalized rehabilitation program in terms of Anxiety and depression [6 months]

    Hospital and Anxiety Depression Scale (from 0 to 42, highers scores mean worse outcome

  35. Impact of a multidisciplinary and personalized rehabilitation program in terms of Anxiety and depression [1 month]

    Pichot asthenia scale (from 0 to 32, highers mean worse outcome)

  36. Impact of a multidisciplinary and personalized rehabilitation program in terms of Anxiety and depression [3 months]

    Pichot asthenia scale (from 0 to 32, highers mean worse outcome)

  37. Impact of a multidisciplinary and personalized rehabilitation program in terms of Anxiety and depression [6 months]

    Pichot asthenia scale (from 0 to 32, highers mean worse outcome)

  38. Impact of a multidisciplinary and personalized rehabilitation program in terms of Healthcare consumption [1 month]

    Number of consultations with the healthcare professionals

  39. Impact of a multidisciplinary and personalized rehabilitation program in terms of Healthcare consumption [3 months]

    Number of consultations with the healthcare professionals

  40. Impact of a multidisciplinary and personalized rehabilitation program in terms of Healthcare consumption [6 months]

    Number of consultations with the healthcare professionals

  41. Impact of a multidisciplinary and personalized rehabilitation program in terms of Healthcare consumption [1 month]

    Rehospitalisation rate (all causes)

  42. Impact of a multidisciplinary and personalized rehabilitation program in terms of Healthcare consumption [3 months]

    Rehospitalisation rate (all causes)

  43. Impact of a multidisciplinary and personalized rehabilitation program in terms of Healthcare consumption [6 months]

    Rehospitalisation rate (all causes)

  44. Impact of a multidisciplinary and personalized rehabilitation program in terms of Medico-economic evaluation [3 months]

    Incremental cost-effectiveness ratio

  45. Impact of a multidisciplinary and personalized rehabilitation program in terms of Medico-economic evaluation [6 months]

    Incremental cost-effectiveness ratio

  46. Patient's opinion concerning the rehabilitation program [3 months]

    Satisfaction questionnaire with open-ended questions (no specific scale is available)

  47. Patient's opinion concerning the rehabilitation program [6 months]

    Satisfaction questionnaire with open-ended questions (no specific scale is available)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hôtel Dieu Paris Paris France
2 Centre Hospitalier de Cornouaille Quimper France
3 CHU Rennes Rennes France
4 Centre Hospitalier de Saint-Brieuc Saint-Brieuc France
5 Centre Hospitalier Bretagne Atlantique Vannes France

Sponsors and Collaborators

  • Rennes University Hospital

Investigators

  • Principal Investigator: Lilian Alix, Dr, Rennes University Hospital
  • Principal Investigator: Aranzazu PEDROSA GONZALEZ, Dr, Centre Hospitalier de Saint-Brieuc
  • Principal Investigator: Christophe POPINEAU, Dr, Centre Hospitalier Bretagne Atlantique
  • Principal Investigator: Patricia THOREUX, Pr, Hôtel Dieu Paris
  • Principal Investigator: Nadia SAIDANI, Dr, Centre Hospitalier de Cornouaille

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Rennes University Hospital
ClinicalTrials.gov Identifier:
NCT04466800
Other Study ID Numbers:
  • 35RC20_9875_RECOVER-19
First Posted:
Jul 10, 2020
Last Update Posted:
Jul 1, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Rennes University Hospital

Study Results

No Results Posted as of Jul 1, 2022