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Use of E-health Based Exercise Intervention After COVID-19

N

Norwegian University of Science and Technology

Status

Active, not recruiting

Conditions

COVID-19

Treatments

Behavioral: Exercise training using an e-health tool

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Reduced subjective and objective functional capacity performance are reported after COVID-19 in a large proportion of subjects. The aim of this study is to examine the feasibility and effect of using an e-health tool for guidance and tracking of exercise training in a general population of adults previously infected by COVID-19.

Full description

Both hospitalized and non-hospitalized persons who have undergone extensive multi-disciplinary rehabilitation programs report significantly improved physical function after rehabilitation. Exercise training may be the key intervention to improve fitness and subjective complaints such as fatigue, low physical fitness and dyspnea after COVID-19 infection. However, traditional group-based exercise training or self-training programs at fitness centers have been shut down during the pandemic, and home-based interventions are warranted. To overcome the limitations and costs of a fitness center/personal trainer-based intervention study, more knowledge on the effectiveness and efficacy of using an e-Health system to recruit, train and monitor participants after illness are needed.

Enrollment

77 patients

Sex

All

Ages

18 to 59 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Persons who have undergone COVID-19 disease
  • People who struggle to be physically active enough as a result of corona disease
  • People who experience reduced physical fitness as a result of corona disease

Exclusion criteria

-- more than 100 PAI per week (calculated from self-reported activity level)

  • uncontrolled hypertension (high blood pressure) (over 200/110).
  • symptomatic valve failure, hypertrophic cardiomyopathy, unstable angina, pulmonary
  • hypertension, heart failure and/or severe rhythm disturbances
  • cancer that makes participation impossible or exercise contraindicated. Considered individually in consultation with the attending physician.
  • chronic contagious infectious diseases.
  • Participates in other studies that are not compatible with participation in this project
  • Post-exertional symptom exacerbation (PESE)/post-exertional malaise (PEM)/post-exertional neuroimmune exhaustion (PENE).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

77 participants in 2 patient groups

Supervised exercise
Experimental group
Treatment:
Behavioral: Exercise training using an e-health tool
Control group
No Intervention group

Trial contacts and locations

1

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Central trial contact

Dorthe Stensvold Stensvold

Data sourced from clinicaltrials.gov

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