The Burden of COVID-19 Survivorship

Sponsor
Mayo Clinic (Other)
Overall Status
Recruiting
CT.gov ID
NCT04913129
Collaborator
(none)
50
1
2
13.9
3.6

Study Details

Study Description

Brief Summary

This research study is being done to find out what the longer-term physiological consequences of COVID-19 are, and to determine if exercise therapy can help improve lung function, heart function and overall fitness, and reduce symptoms in people recovering from SARS-CoV-2.

Condition or Disease Intervention/Treatment Phase
  • Other: Exercise Training
N/A

Detailed Description

The purpose of this research is to see if taking part in structured exercise training will improve the ability to exercise, the function of the lungs and the function of the heart, and reduce symptoms of fatigue and breathlessness in people recovering from COVID-19. After enrollment all patients will complete exercise testing, lung function testing, and cardiac imaging. Patients will be randomized to either 8 weeks of exercise training (4-5 times per week) or will continue standard medical care. All patients will undergo detailed exercise testing, lung function testing, and cardiac imaging after the intervention.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Burden of COVID-19 Survivorship: Exercise Therapy to Combat the Sequelae of COVID-19
Actual Study Start Date :
Nov 4, 2021
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control Group

Standard physician-guided medical care after COVID-19

Experimental: Interventional (exercise training) Group

8 week home-based exercise training

Other: Exercise Training
8 week home-based exercise therapy 4-5 times/week

Outcome Measures

Primary Outcome Measures

  1. Maximal oxygen update (VO2max) measured in mL/kg/min [8 weeks]

    VO2max is the maximal oxygen consumed during an exhaustive exercise test

Secondary Outcome Measures

  1. Peak exercise work rate (Wpeak) measured in Watts [8 weeks]

    Wpeak is the highest achieved power during a maximal incremental cycle exercise test

  2. Forced vital capacity (FVC) measured in L [8 weeks]

    FVC is the largest amount of air that can be exhaled from the lungs in one maximal breath

  3. Forced expiratory volume in 1 second (FEV1) measured in L [8 weeks]

    FEV1 is the largest amount of air that can be exhaled from the lungs in the first second of one maximal breath

  4. Maximal inspiratory pressure (MIP) measured in cmH2O [8 weeks]

    Highest inspiratory muscle pressure (i.e. inspiratory muscle strength) during a maximal inspiratory effort

  5. Maximal expiratory pressure (MEP) measured in cmH2O [8 weeks]

    Highest expiratory muscle pressure (i.e. expiratory muscle strength) during a maximal expiratory effort

  6. Left ventricular contractile function measured as % fractional area change (LV FAC) [8 weeks]

    LV FAC is a measure of overall contractile function of the LV

  7. Right ventricular contractile function measured as % fractional area change (RV FAC) [8 weeks]

    RV FAC is a measure of overall contractile function of the RV

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Aged 21 to 75 years.

  • History of RT-PCR proven SARS-CoV-2 infection.

  • Deemed 'recovered' from SARS-CoV-2 infection.

  • Not clinically obese (BMI ≥ 36) and/or suffer from musculoskeletal or other conditions that would limit exercise participation.

  • No evidence of cardiac ischemia at rest or during exertion (via ECG).

  • Able to provide written informed consent.

Exclusion Criteria:
  • Individuals less than 21 or more than 75 years old.

  • Not able to take part in structured exercise training due to injury or other conditions that would put person at risk during exercise.

  • Unable to provide written informed consent.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mayo Clinic in Florida Jacksonville Florida United States 32224

Sponsors and Collaborators

  • Mayo Clinic

Investigators

  • Principal Investigator: Bryan Taylor, PhD, Mayo Clinic

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Bryan Taylor, Principal Investigator, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT04913129
Other Study ID Numbers:
  • 21-002693
First Posted:
Jun 4, 2021
Last Update Posted:
Dec 8, 2021
Last Verified:
Dec 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 8, 2021