NCT07651371

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
74

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2021

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
2.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 15, 2023

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 15, 2024

Completed
1.4 years until next milestone

First Submitted

Initial submission to the registry

May 28, 2026

Completed
19 days until next milestone

First Posted

Study publicly available on registry

June 16, 2026

Completed
Last Updated

June 16, 2026

Status Verified

June 1, 2026

Enrollment Period

2.9 years

First QC Date

May 28, 2026

Last Update Submit

June 12, 2026

Conditions

Keywords

Reabilitação Físicatrial clinicfunctionalitylaboratory tests

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

EXPERIMENTAL

Before-and-after treatment

Other: Physical rehabilitationDevice: Treadmill ergometerDevice: Pulley

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.

treatment

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)

treatment
PulleyDEVICE

Variable Resistance Machines

treatment

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Post-Acute COVID-19 Syndrome

Condition Hierarchy (Ancestors)

COVID-19Pneumonia, ViralPneumoniaRespiratory Tract InfectionsInfectionsVirus DiseasesCoronavirus InfectionsCoronaviridae InfectionsNidovirales InfectionsRNA Virus InfectionsLung DiseasesRespiratory Tract DiseasesPost-Infectious DisordersChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: This is an experimental analytical study in the form of an uncontrolled clinical trial conducted in accordance with the TREND guidelines. The present study was conducted at the Cardiorespiratory Diseases Outpatient Clinic (UEAFTO/UEPA). The Cardiorespiratory Diseases Outpatient Clinic is located at the UEAFTO campus of UEPA, in the city of Belém. The clinic integrates teaching, research, and outreach activities and serves as a reference center for the clinical and multidisciplinary care of patients with cardiorespiratory diseases, including infectious diseases, referred from the state public health system. Clinical muscle and functional assessments were performed at this facility.
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

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.

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

Locations