Effects of a Physical Rehabilitation Program on Long COVID
ReabCovid
Clinical, Functional, and Laboratory Outcomes of a Physical Rehabilitation Program for the Treatment of Long COVID: A Non-Controlled Clinical Trial
1 other identifier
interventional
74
1 country
1
Brief Summary
The objective of this clinical trial is to analyze the clinical, functional, and laboratory effects of a rehabilitation protocol designed for patients with long COVID; it may include any of the following: sex/gender, age groups, healthy volunteers. The main questions it aims to answer are: Does handgrip strength improve after the intervention? Does the 6-minute walk test improve after the intervention? Participants must attend all 20 sessions of the physical rehabilitation program.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jan 2021
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 5, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 15, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
December 15, 2024
CompletedFirst Submitted
Initial submission to the registry
May 28, 2026
CompletedFirst Posted
Study publicly available on registry
June 16, 2026
CompletedJune 16, 2026
June 1, 2026
2.9 years
May 28, 2026
June 12, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
hand grip strength
Handgrip strength (HGS) was measured using a CROW model manual hydraulic dynamometer. The test was conducted in accordance with the recommendations of the American Society of Hand Therapists (ASTH).
Through the end of the 20 sessions (up to 10 weeks)
Study Arms (1)
treatment
EXPERIMENTALBefore-and-after treatment
Interventions
The multidisciplinary rehabilitation program consisted of 20 in-person sessions, each lasting 50 minutes, divided into four phases of progressive load. All sessions were structured in three stages: warm-up, the training itself, and cool-down. The warm-up consisted of 10 minutes of stretching exercises. During the training stage (30 minutes), participants walked on a treadmill for 15 minutes, with intensity controlled by reserve heart rate (HR), progressing from 50% (sessions 1-5) to 60% (6-10), 70% (sessions 11-15), and reaching 80% in the final sessions (16-20). Respiratory muscle training (RMT) was performed with an initial load of 25% of Peak Inspiratory Pressure (PPeak), progressing to 30% starting from the 11th session, with variations in volume ranging from 3 sets of 12 repetitions to 4 sets of 15 repetitions throughout the phases.
Participants walked on a treadmill for 15 minutes, with intensity controlled by reserve heart rate (HR), progressing from 50% (sessions 1-5) to 60% (6-10), 70% (sessions 11-15), and reaching 80% in the final sessions (16-20)
Eligibility Criteria
You may qualify if:
- patients of both sexes,
- aged 18 years or older,
- diagnosed with long COVID;
You may not qualify if:
- pregnant women,
- individuals with special needs,
- patients who refuse to sign the informed consent form.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ambulatório de Doenças Cardiorrespiratórias (UEAFTO/UEPA)
Belém, Pará, Brazil
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Clinical Professor
Study Record Dates
First Submitted
May 28, 2026
First Posted
June 16, 2026
Study Start
January 5, 2021
Primary Completion
December 15, 2023
Study Completion
December 15, 2024
Last Updated
June 16, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- SAP
- Time Frame
- 01/01/2025 a 01/01/2028
- Access Criteria
- Access will be granted to members of the research group, and only the spreadsheets without individual identifiers
After the data is collected and entered into a spreadsheet, each participant's identifying information will be converted into codes and then shared with members of the research team.