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Clinical Trials/NCT05373407
NCT05373407
Completed
Not Applicable

A Randomized Controlled Trial Examining the Impact of Low Versus Moderate-intensity Aerobic Training in Post-discharge COVID-19 Older Subjects

University of Hail1 site in 1 country72 target enrollmentAugust 15, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COVID-19
Sponsor
University of Hail
Enrollment
72
Locations
1
Primary Endpoint
Post-Covid Functional Scale (PCFS)
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The main purpose of this study is to compare the impact of low versus moderate-intensity aerobic training in post-COVID 19 older subjects.

On exercise adherence and changes in physical fitness, psychological status, and quality of life after a 10-week intervention.

Registry
clinicaltrials.gov
Start Date
August 15, 2022
End Date
December 1, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ahmed Abdelmoniem Ibrahim

Associate professor

University of Hail

Eligibility Criteria

Inclusion Criteria

  • Age range of 60 - 80 years with
  • diagnosis of post-COVID-19

Exclusion Criteria

  • • History of lower limb surgeries, fractures
  • Cardiac problems
  • Respiratory problems
  • Neurological problems
  • Systemic problems and any other contraindications for aerobic training

Outcomes

Primary Outcomes

Post-Covid Functional Scale (PCFS)

Time Frame: 8 weeks

This scale measures the functional state and Independence of patients after COVID-19 infection. The scale includes two items scored from 0-4 and 0-5. A high value indicates more restrictions in function and independence during daily life.

Distance walked in the 6-min walk test (6 MWT)

Time Frame: 8 weeks

The 6-min walk test (6 MWT) measures the distance that a patient can quickly walk on a flat, hard surface in a period of 6 minutes (the 6MWD). (ATS Statement: Guidelines for the Six-Minute Walk Test, Am J Respir Crit Care Med, 2002)

Secondary Outcomes

  • Quality of life SF-36(8 weeks)
  • Number of repetitions performed in a 1-min Sit-to-Stand (STS) test(8 weeks)
  • 2. Anxiety and Depression evaluated by the HAMLITON ScAnxiety and Depressionale (HADS)(8 weeks)

Study Sites (1)

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