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Rehabilitation of Fatigue in Patients With Post-COVID-19 Syndrome (COVIDATE-02)

U

University of Granada (UGR)

Status

Completed

Conditions

Post-COVID-19 Syndrome

Treatments

Behavioral: Virtual reality based rehabilitation
Behavioral: Rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT06814379
COVIDATE-02

Details and patient eligibility

About

More than half of patients with post-COVID-19 syndrome experience fatigue. Rehabilitation is needed to treat this persistent symptom.

The aim of this study is to conduct a rehabilitation intervention to treat patients with post-COVID-19 syndrome who experience persistent fatigue.

Full description

  • Background: More than half of patients with post-COVID-19 syndrome experience fatigue. Rehabilitation is needed to treat this persistent symptom.
  • Objectives: To conduct a rehabilitation intervention to treat patients with post-COVID-19 syndrome who experience persistent fatigue.
  • Methodology: Randomized clinical trial. There will be 3 groups.
  • Patients will be recruited from the Virgen de las Nieves University Hospital in Granada.
  • The evaluation will be carried out at the University of Granada.
  • The rehabilitation will be carried out at the University of Granada and/or patient's home.

Enrollment

54 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • diagnosis of COVID-19
  • post-COVID-19 syndrome
  • adults ≥ 18 y < 75 años
  • be medically stable
  • to be able to walk
  • not currently participating in a rehabilitation programme and/or other study.
  • fatigue: FSS ≥ 36 puntos
  • basic knowledge
  • wish to participate in the study and sign the informed consent

Exclusion criteria

  • patients with severe comorbidities that interfere with the ability to perform the study
  • patients with mental, physical or organic problems that under medical criteria may pose a risk to the patient

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

54 participants in 3 patient groups

Control group
No Intervention group
Description:
Not intervention
Rehabilitation
Experimental group
Description:
30-60 minutes. A total of 3 session/week at home. 4 weeks. * Warm-up. * Aerobic: walking (20-25 minutes). * Strength: (25-30 minutes). * Cooling. * Education: WHO recommendations.
Treatment:
Behavioral: Rehabilitation
Virtual reality based rehabilitation
Experimental group
Description:
30-60 minutes. A total of 3 session/week (2 sessions at home and 1 session at the University of Granada). 4 weeks. The 2 sessions at home will be the same as the sessions in the rehabilitation group (group 2). The session at the University of Granada will be done with virtual reality (Nintendo Switch) and will follow the same outline as the rest of the sessions: * Warm-up. * Aerobic: walking (20-25 minutes). * Strength: (25-30 minutes). * Cooling. * Education: WHO recommendations.
Treatment:
Behavioral: Virtual reality based rehabilitation

Trial contacts and locations

1

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Central trial contact

Irene Torres Sánchez

Data sourced from clinicaltrials.gov

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