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Clinical Trials/NCT02404831
NCT02404831CompletedPhase 1

An Evaluation of Web Based Pulmonary Rehabilitation- Pilot Study

University of Glasgow2 sites in 1 country20 target enrollmentStarted: April 2014Last updated:
Conditions

Trial Snapshot

Phase
Phase 1
Status
Completed
Enrollment
20
Locations
2
Primary Endpoint
Change from baseline in Shuttle Walk test at 6 weeks

Study Overview

Brief Summary

The purpose of this pilot study is to compare a six week web-based pulmonary rehabilitation programme with traditional hospital-based pulmonary rehabilitation classes for people affected by COPD.

Detailed Description

Chronic Obstructive Pulmonary Disease (COPD) is a term used to describe a number of lung conditions characterised by irreversible damage to the airways causing airflow obstruction. Pulmonary Rehabilitation (PR) is a broad programme that helps improve the health and well-being of people with breathing difficulties, most commonly COPD. Participation in PR leads to improvements in exercise tolerance and functional ability, as well as a reducing breathlessness in everyday activities. It is traditionally an outpatient programme based in a hospital or community setting run by a multidisciplinary team, and usually lead by physiotherapy and nursing staff. Typically it includes a physical exercise programme, and advice and education on managing a chronic lung condition. The purpose of this pilot study is to compare a six week web-based pulmonary rehabilitation programme with traditional hospital-based pulmonary rehabilitation classes for people affected by COPD.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • A diagnosis of COPD
  • Suitable for participation in the NHS Lanarkshire PR programme
  • Independently mobile
  • Access to the internet in their own home

Exclusion Criteria

  • Unstable cardiac or other health problems which may prevent participation in study
  • Under the age of 18
  • Unable to read/understand English
  • Unwilling to be randomised into PR delivered via the hospital or internet

Outcomes

Primary Outcomes

Change from baseline in Shuttle Walk test at 6 weeks

Time Frame: 6 weeks

analysis

Secondary Outcomes

  • Change from baseline in Chronic Disease Questionnaire at 6 weeks(6 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dr Lorna Paul

Dr

University of Glasgow

Study Sites (2)

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