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An Evaluation of Web Based Pulmonary Rehabilitation

An Evaluation of Web Based Pulmonary Rehabilitation- Pilot Study

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02404831
Acronym
webbasedPR
Enrollment
20
Registered
2015-04-01
Start date
2014-04-30
Completion date
2015-05-31
Last updated
2015-07-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease

Keywords

Physiotherapy, Pulmonary Rehabilitation, Exercise, Telerehab

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.

Interventions

OTHERWeb-based PR

Participants will undertake web-based PR twice/week for 6 weeks in their own home. They will be given individual log-in details to access the website with access to exercises and education pages. Participants will be provided with a standardised exercise programme at the start of the study. The level of intensity of exercises will be progressed as appropriate on an individual basis for all participants in the group. Participant log-ins and diaries will be monitored remotely and participants will be telephone at weeks 2 and 4 by their physiotherapist to discuss their progress and, at this time, exercises may be progressed by changing the level of difficulty/intensity. This is done remotely by physiotherapy staff.

OTHERHospital-based PR

Participants allocated to this group will undertake hospital-based PR twice per week for 6 weeks in. Participants attend PR classes and complete a circuit based exercise class. The level of intensity of exercises will be progressed as appropriate on an individual basis for all participants in the group. Following each class they will receive educational information about their condition.

Sponsors

NHS Research and Development
CollaboratorOTHER_GOV
University of Glasgow
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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 * Pregnant * Unable to read/understand English * Unwilling to be randomised into PR delivered via the hospital or internet

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in Shuttle Walk test at 6 weeks6 weeksanalysis

Secondary

MeasureTime frameDescription
Change from baseline in Chronic Disease Questionnaire at 6 weeks6 weeksquestionnaire

Other

MeasureTime frameDescription
Change from baseline in Hospital Anxiety and Depression Scale at 6 weeks6 weeks
Change from baseline in Borg Breathlessness Scale at 6 weeks6 weeks
Website evaluation questionnaire6 weeksquestionnaire completed by Experimental Group only
Semi-structured telephone interviews6 weeksQualitative interview conducted with Experimental Group only

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026