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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00168285
Date of registration: 13/09/2005
Primary sponsor: The Alfred
Public title: Pulmonary Rehabilitation in Interstitial Lung Disease
Scientific title: Pulmonary Rehabilitation in Interstitial Lung Disease - a Multi-Centre, Single-Blinded Randomised Controlled Trial
Date of first enrolment: March 2005
Target sample size: 56
Recruitment status: Active, not recruiting
URL:  http://clinicaltrials.gov/show/NCT00168285
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment  
Countries of recruitment
Australia
Contacts
Name:   Anne E Holland, PhD
Address: 
Telephone:
Email:
Affiliation:  Alfred Hospital and LaTrobe University
Name:   Catherine Hill, PhD
Address: 
Telephone:
Email:
Affiliation:  Austin Hospital, Melbourne Australia
Name:   Christine McDonald, MBBS PhD
Address: 
Telephone:
Email:
Affiliation:  Austin Hospital, Melbourne Australia
Name:   Matthew Conron, MBBS
Address: 
Telephone:
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Affiliation:  The Alfred
Name:   Prue Munro, BAppSc
Address: 
Telephone:
Email:
Affiliation:  The Alfred
Key inclusion & exclusion criteria

Inclusion Criteria:

- Ambulant

- Stable medical therapy

- Dyspnoea on exertion following maximal treatment

Exclusion Criteria:

- A history of syncope on exertion

- Too unwell to attend the hospital for exercise training

- Any other comorbidities which would prevent exercise training

- Previous Pulmonary Rehabilitation in the last 12 months



Age minimum: 40 Years
Age maximum: 90 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Interstitial Lung Disease
Intervention(s)
Behavioral: Pulmonary Rehabilitation
Primary Outcome(s)
Functional exercise capacity
Secondary Outcome(s)
Dyspnoea
Health-related quality of life
Maximal exercise capacity
Secondary ID(s)
PRIDe
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Austin Hospital, Melbourne Australia
La Trobe University
Victorian Tuberculosis and Lung Association
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