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Exercise Training Using an App on Physical Cardiovascular Function Individuals With Post-covid-19 Syndrome (Recovery)

U

University of Nove de Julho

Status

Enrolling

Conditions

Post-Acute COVID-19 Syndrome

Treatments

Behavioral: Exercise
Behavioral: Control

Study type

Interventional

Funder types

Other

Identifiers

NCT06168006
Recovery Long Covid

Details and patient eligibility

About

The aim of this study is to assess the effect of a physical exercise program via a mobile application on functional parameters in individuals with post-COVID-19 syndrome. This is a clinical trial involving 60 individuals with post-COVID syndrome who will be randomly assigned to either a control group (physical activity guideline) or an experimental group (app-based training).

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Laboratory diagnosis of COVID-19
  • Fatigue ≥ 8 points on the Chalder Scale and/or dyspnea 2-4 on the Modified Medical Research Council
  • Have access to a smartphone
  • Have no contraindications for exercise practice
  • Have ability to sit and stand and maintain balance while standing
  • Have preserved cognitive function
  • Have no risk of falls according to the Morse Fall Scale

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Exercise intervention
Experimental group
Description:
The subjects randomized to this group will perform three app-based training sessions per week for 12 weeks, each session lasting a maximum of 40 minutes.
Treatment:
Behavioral: Exercise
Control intervention
Sham Comparator group
Description:
This group will receive a booklet with exercise instructions, and will be recommended the same frequency and duration of exercise as the experimental group
Treatment:
Behavioral: Control

Trial contacts and locations

1

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Central trial contact

Raphael Ritti-Dias, PhD; Fernanda Corrêa, PhD

Data sourced from clinicaltrials.gov

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