CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 30 enrolled
Drug / intervention
Out-patient Pulmonary Rehabilitationother
Likely dose
Not stated in record
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Search/NCT05736939
NCT05736939N/ACompleted

Gender Differences in the Recovery Rate Following a Hybrid Pulmonary Rehabilitation Programme in Patients With Long COVID-19 Syndrome

National and Kapodistrian University of Athens·observational·Posted Feb 21, 2023·Updated Oct 11, 2023

In Brief

An observational study evaluating Out-patient Pulmonary Rehabilitation for Post Acute COVID-19 Syndrome. Completed, enrolled 30 participants across 1 site.

Detailed Summary

The goal of this retrospective analysis is to compare the magnitude of improvement in respiratory and peripheral muscle strength, following the completion of a hybrid pulmonary rehabilitation programme, in men and women with long COVID-19 syndrome. The main question it aims to answer is the following: • does gender limits the effects of a hybrid pulmonary rehabilitation programme on respiratory and peripheral muscle strength?

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesGreece
Collaborators--

Timeline

N/ACompletedFinished
2023202420252026
First PostedFeb 21, 2023
Enrollment StartOct 1, 2022
Primary CompletionFeb 28, 2023
Study CompletionMar 15, 2023
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 3.4 years ago

Interventions

Out-patient Pulmonary Rehabilitationother

Pulmonary Rehabilitation (PR) programme consisting of 30 minutes interval aerobic exercise on cycle ergometers at 100% of peak work rate (WRpeak) and resistance exercises for the upper body. Dyspnoea and leg discomfort were recorded on the modified 1-10 Borg scale, whereas heart rate (HR) and oxygen saturation (SpO2%) were monitored by a pulse oximeter. Based on symptoms of breathlessness and fatigue reported at the end of each session, the exercise intensity was increased by 5-10% of the baseline WRpeak in the next session. The remote 24 home-based PR sessions consisted of 30 minutes walking with an individualised target of steps, recorded via the mobile app installed in the patients' mobile phone. The steps, leg discomfort and dyspnoea were reported by the patient via a physical activity diary on a weekly basis. If dyspnoea and fatigue were both \<4 at the Borg scale the weekly target of steps was increased by 5-10% by the assessors.