A 12 Week Physical Training Programme for Patients With Chronic Obstructive Pulmonary Disease
2 other identifiers
interventional
22
1 country
1
Brief Summary
The purpose of this study is to determine whether water based or land based group training is more effective for people with COPD.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable chronic-obstructive-pulmonary-disease
Started Feb 2008
Typical duration for not_applicable chronic-obstructive-pulmonary-disease
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2008
CompletedFirst Submitted
Initial submission to the registry
August 29, 2008
CompletedFirst Posted
Study publicly available on registry
September 1, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2009
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2010
CompletedMarch 7, 2022
February 1, 2022
1.2 years
August 29, 2008
February 18, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
VO2 peak
12 weeks
Secondary Outcomes (1)
Health related quality of life
12 weeks
Study Arms (2)
B1
EXPERIMENTALB1 - training in water
S1
EXPERIMENTALS1 - training on land
Interventions
45 minutes interval training in water, submaximal intensity, twice a week
45 minutes interval training on land, submaximal intensity, twice a week
Eligibility Criteria
You may qualify if:
- COPD GOLD II
- Not taking part in physical activity during the last year
You may not qualify if:
- COPD GOLD I, III, IV
- Pain in the legs that make activity difficult
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Norwegian University of Science and Technologylead
- Helse Nord-Trøndelag HFcollaborator
- Nord-Trøndelag University Collegecollaborator
Study Sites (1)
Levanger Hosp
Levanger, Nord-Trøndelag, 7600, Norway
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Thor Naustdal, MD
Hospital of Levanger / NTNU ISB
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 29, 2008
First Posted
September 1, 2008
Study Start
February 1, 2008
Primary Completion
May 1, 2009
Study Completion
September 1, 2010
Last Updated
March 7, 2022
Record last verified: 2022-02
Data Sharing
- IPD Sharing
- Will not share