Skip to main content
Clinical Trials/ACTRN12622001501730
ACTRN12622001501730
Recruiting
未知

Implementing Pulmonary Rehabilitation in Primary care: Feasibility, acceptability, and safety

niversity of Sydney0 sites91 target enrollmentDecember 1, 2022

Overview

Phase
未知
Intervention
Not specified
Conditions
Chronic obstructive pulmonary disease (COPD)
Sponsor
niversity of Sydney
Enrollment
91
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 1, 2022
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Clinician participants:
  • AHPRA registered physiotherapist or Exercise \& Sports Science Australia accredited exercise physiologist
  • Working in private practice where:
  • oAt least two staff (clinical or administrative) are present during assessments or group exercise sessions
  • oThere is adequate space for group exercise (minimum 3 participants) to occur
  • oAccessible for people with chronic respiratory disease
  • Willing to provide intervention for part two of study (twice weekly PR for 8\-weeks)
  • Have or be willing to obtain current CPR training prior to assessing any study participants
  • Patient participants:
  • Age greater than 18 years

Exclusion Criteria

  • Clinician participants:
  • Physiotherapists or AEPs with significant prior PR experience (more than one rotation as Level 1 clinician, or delivery of Lungs in Action)
  • Physiotherapists or AEPs with post\-graduate cardiopulmonary qualifications
  • Patient participants:
  • Exacerbation of respiratory disease within 4 weeks prior to recruitment
  • Completed PR in the past year
  • Prescribed home supplemental oxygen or requiring supplemental oxygen for exercise (desaturates \< 80% SpO2 on field walking test)
  • Medical conditions that contraindicate safe group exercise outside hospital setting (e.g. unstable cardiac disease, severe musculoskeletal impairments)
  • Unable to provide informed consent

Outcomes

Primary Outcomes

Not specified

Similar Trials