Rehabilitation of Fatigue in Patients With Post-COVID-19 Syndrome
NCT ID: NCT06814379
Last Updated: 2026-01-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
54 participants
INTERVENTIONAL
2025-02-03
2025-07-31
Brief Summary
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The aim of this study is to conduct a rehabilitation intervention to treat patients with post-COVID-19 syndrome who experience persistent fatigue.
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Detailed Description
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* 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.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Control group
Not intervention
No interventions assigned to this group
Rehabilitation
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.
Rehabilitation
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.
Virtual reality based rehabilitation
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.
Virtual reality based rehabilitation
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.
Interventions
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Rehabilitation
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.
Virtual reality based rehabilitation
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.
Eligibility Criteria
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Inclusion Criteria
* 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 mental, physical or organic problems that under medical criteria may pose a risk to the patient
18 Years
75 Years
ALL
No
Sponsors
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Universidad de Granada
OTHER
Responsible Party
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Irene Torres Sánchez
PT, PhD, Principal Investigator
Principal Investigators
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Irene Torres Sánchez, PhD
Role: PRINCIPAL_INVESTIGATOR
Universidad de Granada
Locations
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University of Granada
Granada, Granada, Spain
Countries
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Other Identifiers
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COVIDATE-02
Identifier Type: -
Identifier Source: org_study_id
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