Actively Recruiting

Age: 18Years +
All Genders
NCT05820776

Tele-rehabilitation in Chronic Respiratory Disease: an Observational Cohort Study

Led by West Park Healthcare Centre · Updated on 2024-07-26

50

Participants Needed

1

Research Sites

142 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Pulmonary rehabilitation is a program that helps people with lung disease improve their function. It uses exercise, education, and self-management strategies to improve physical ability and quality of life. Because some people are unable to visit West Park Healthcare Centre, we established a remote supervised pulmonary rehabilitation program that patients can access via an electronic device (computer, tablet or smart phone). Regular quality assurance is necessary to ensure that the program is effective. We plan to collect and summarize the program's results. The benefit of doing so is that it allows us to make any changes or improvements that may help patients with chronic respiratory conditions.

CONDITIONS

Official Title

Tele-rehabilitation in Chronic Respiratory Disease: an Observational Cohort Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Stable chronic respiratory disease
  • Qualified candidates for pulmonary rehabilitation
  • Current non-smoker
  • Primary diagnosis chronic respiratory disease limited by dyspnea (mMRC 62 2)
  • Free of exacerbation at the time of admission
  • Stable co-existing conditions
Not Eligible

You will not qualify if you...

  • Completed pulmonary rehabilitation within the previous 12 months of the current admission
  • Unable to communicate with the treating team

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

West Park Healthcare Centre

Toronto, Ontario, Canada, M6M 2J5

Actively Recruiting

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Research Team

R

Research Assistant

CONTACT

O

Office Supervisor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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