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SCOPE-Study: Salzburg Chronic Obstructive Pulmonary Disease- Exercise and Oxygen Study (SCOPE)

Primary Purpose

Chronic Obstructive Pulmonary Disease

Status
Completed
Phase
Phase 4
Locations
Austria
Study Type
Interventional
Intervention
Physical exercise training with supplemental oxygen
Physical exercise training with "room air supplementation"
Sponsored by
Paracelsus Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease focused on measuring Lung Diseases, Obstructive, Respiratory Tract Diseases, Lung Diseases, Respiration Disorders, Pulmonary Disease, Chronic Obstructive, COPD, Chronic Obstructive Lung Disease, Chronic Obstructive Airway Disease, Chronic Airflow Obstruction, oxygen, oxygen supplementation

Eligibility Criteria

30 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • COPD with FEV1 pred. 30 to 60%, PO2 at rest > 55 mmHg and PCO2 < 45 mm Hg
  • age: > 30 years

Exclusion Criteria:

  • Musculoskeletal disease, which prohibits training
  • Relevant neoplastic disease with cachexia
  • Expected non compliance with the study protocol due to drug and alcohol abuse
  • Coronary heart disease defined by angina pectoris or relevant ST-changes during exercise or myocardial infarction in the last 6 months
  • Left ventricular ejection fraction < 40 %
  • Renal insufficiency with creatinine > 2 mmol/liter
  • Symptomatic intermittent claudication or peripheral neuropathy
  • Anaemia < 10 mg/dl or red blood count < 3 Mio/mm3

Sites / Locations

  • Institute of Sports Medicine, Prevention and Rehabilitation, Paracelsus Medical University Salzburg

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

group RO (Room air / Oxygen)

group OR (Oxygen / Room air)

Arm Description

RO (Room air / Oxygen): First 6 weeks of exercise training under normoxic conditions (Room air), followed by 6 weeks of exercise training with oxygen supplementation.

OR (Oxygen / Room air): First 6 weeks of exercise training with oxygen supplementation, followed by 6 weeks of exercise training under normoxic conditions (room air).

Outcomes

Primary Outcome Measures

Exercise capacity (Watts/kg)
To investigate the effectiveness of physical training in COPD- patients comparing a 6 week period of exercise under oxygen supplementation with a 6 week period of exercise under "room air supplementation".

Secondary Outcome Measures

Quality of life
Measured by St. George Respiratory Questionnaire
Maximal oxygen uptake (VO2-max)
Measurement of spiroergometry
Heart rate, blood pressure and exercise capacity at lactate-thresholds 2,3 and 4.
Measurement of ergometry
BODE-index
The BODE index is a simple multidimensional grading system for COPD-patients which considers body-mass index, degree of airflow obstruction (FEV1) and dyspnea (BORG scale), and exercise capacity, which will be measured by the six-minute-walk test.
Walking capacity
6-minute-walk test
Dyspnea
Measured by BORG-scale
Body composition
Body composition/muscle volume will be measured using magnetic resonance imaging.
Blood parameters of inflammation
Inflammatory changes will be assessed via blood test analysis.
Vascular changes
Vascular changes will be assessed via blood test analysis as well as analysis of endothelial function.
ten repetition maximum
The ten repetition maximum (10-RM) is a measure of the maximal weight a subject can lift 10 times.

Full Information

First Posted
June 24, 2010
Last Updated
October 30, 2013
Sponsor
Paracelsus Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT01150383
Brief Title
SCOPE-Study: Salzburg Chronic Obstructive Pulmonary Disease- Exercise and Oxygen Study
Acronym
SCOPE
Official Title
The Effect of Supplemental Oxygen During Physical Exercise Training on Exercise Capacity in COPD Patients.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2013
Overall Recruitment Status
Completed
Study Start Date
July 2010 (undefined)
Primary Completion Date
July 2013 (Actual)
Study Completion Date
July 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Paracelsus Medical University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Chronic obstructive pulmonary disease (COPD) is number four of the leading causes of death in the USA and Europe. Moreover, among the top five causes of death, this disease is the only one with increasing mortality rates. Physical training has become an evidence based therapeutic intervention in these patients. In this study the investigators aim to establish if supplemental oxygen during strength and endurance training improves exercise tolerance. Furthermore, the investigators want to research, if supplemental oxygen has the ability to increase training intensity, which would lead to a greater training effect with respect to respiratory, vascular, inflammatory and anthropometric parameters, as well as quality of life. SCOPE is a prospective, randomized, double-blinded, controlled, cross-over trial. The investigators aim to enroll 40 patients suffering from COPD aged >30 years. Inclusion criteria are FEV1 30-60%, and PO2 at rest >55 mmHg. At baseline, patients will undergo pre-tests including pulmonary, exercise physiological and medical investigations. Prior to the exercise training, an intervention-free control period with usual care is planned. This will be followed by 2 x 6 weeks with physical training (ergometer based endurance training and strength training, using weight lifting machines) with either supplemental oxygen or usual room air (e.g.: first 6 weeks of exercise with oxygen supplementation followed by 6 weeks of room air). After the initial control period and between these two exercise periods, patients will be tested as described in pre-tests, and at the end of the second exercise training period. In addition, the investigators will assess changes in lung function and symptomatic dyspnoea, as well as in quality of life (St. George's Respiratory Questionnaire). Within this study, the investigators hope to improve rehabilitation programs for COPD patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease
Keywords
Lung Diseases, Obstructive, Respiratory Tract Diseases, Lung Diseases, Respiration Disorders, Pulmonary Disease, Chronic Obstructive, COPD, Chronic Obstructive Lung Disease, Chronic Obstructive Airway Disease, Chronic Airflow Obstruction, oxygen, oxygen supplementation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
group RO (Room air / Oxygen)
Arm Type
Active Comparator
Arm Description
RO (Room air / Oxygen): First 6 weeks of exercise training under normoxic conditions (Room air), followed by 6 weeks of exercise training with oxygen supplementation.
Arm Title
group OR (Oxygen / Room air)
Arm Type
Active Comparator
Arm Description
OR (Oxygen / Room air): First 6 weeks of exercise training with oxygen supplementation, followed by 6 weeks of exercise training under normoxic conditions (room air).
Intervention Type
Other
Intervention Name(s)
Physical exercise training with supplemental oxygen
Other Intervention Name(s)
training, physical training, exercise
Intervention Description
Prior to the exercise training, an intervention-free control period with usual care is planned. Intervention group with oxygen supplementation: Endurance training (performed within 70-80% of the heart rate at the anaerobic threshold) as well as strength training will be performed with oxygen supplementation. After 6 weeks of intervention with oxygen supplementation, second intervention period will start with room air instead of oxygen supplementation (as described above).
Intervention Type
Other
Intervention Name(s)
Physical exercise training with "room air supplementation"
Other Intervention Name(s)
training, physical training, exercise
Intervention Description
Prior to the exercise training, an intervention-free control period with usual care is planned. Intervention group with room air supplementation: Endurance training (performed within 70-80% of the heart rate at the anaerobic threshold) as well as strength training will be performed under normoxic conditions. After 6 weeks of intervention with room air, second intervention period will start with oxygen supplementation instead of room air (as described above).
Primary Outcome Measure Information:
Title
Exercise capacity (Watts/kg)
Description
To investigate the effectiveness of physical training in COPD- patients comparing a 6 week period of exercise under oxygen supplementation with a 6 week period of exercise under "room air supplementation".
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Quality of life
Description
Measured by St. George Respiratory Questionnaire
Time Frame
6 weeks
Title
Maximal oxygen uptake (VO2-max)
Description
Measurement of spiroergometry
Time Frame
6 weeks
Title
Heart rate, blood pressure and exercise capacity at lactate-thresholds 2,3 and 4.
Description
Measurement of ergometry
Time Frame
6 weeks
Title
BODE-index
Description
The BODE index is a simple multidimensional grading system for COPD-patients which considers body-mass index, degree of airflow obstruction (FEV1) and dyspnea (BORG scale), and exercise capacity, which will be measured by the six-minute-walk test.
Time Frame
6 weeks
Title
Walking capacity
Description
6-minute-walk test
Time Frame
6 weeks
Title
Dyspnea
Description
Measured by BORG-scale
Time Frame
6 weeks
Title
Body composition
Description
Body composition/muscle volume will be measured using magnetic resonance imaging.
Time Frame
6 weeks
Title
Blood parameters of inflammation
Description
Inflammatory changes will be assessed via blood test analysis.
Time Frame
6 weeks
Title
Vascular changes
Description
Vascular changes will be assessed via blood test analysis as well as analysis of endothelial function.
Time Frame
6 weeks
Title
ten repetition maximum
Description
The ten repetition maximum (10-RM) is a measure of the maximal weight a subject can lift 10 times.
Time Frame
6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: COPD with FEV1 pred. 30 to 60%, PO2 at rest > 55 mmHg and PCO2 < 45 mm Hg age: > 30 years Exclusion Criteria: Musculoskeletal disease, which prohibits training Relevant neoplastic disease with cachexia Expected non compliance with the study protocol due to drug and alcohol abuse Coronary heart disease defined by angina pectoris or relevant ST-changes during exercise or myocardial infarction in the last 6 months Left ventricular ejection fraction < 40 % Renal insufficiency with creatinine > 2 mmol/liter Symptomatic intermittent claudication or peripheral neuropathy Anaemia < 10 mg/dl or red blood count < 3 Mio/mm3
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Josef Niebauer, MD, PhD, MBA
Organizational Affiliation
Institute of Sports Medicine, Prevention and Rehabilitation, Paracelsus Medical University Salzburg
Official's Role
Study Chair
Facility Information:
Facility Name
Institute of Sports Medicine, Prevention and Rehabilitation, Paracelsus Medical University Salzburg
City
Salzburg
ZIP/Postal Code
5020
Country
Austria

12. IPD Sharing Statement

Citations:
PubMed Identifier
18492053
Citation
Vogiatzis I, Athanasopoulos D, Stratakos G, Garagouni C, Koutsoukou A, Boushel R, Roussos C, Zakynthinos S. Exercise-induced skeletal muscle deoxygenation in O-supplemented COPD patients. Scand J Med Sci Sports. 2009 Jun;19(3):364-72. doi: 10.1111/j.1600-0838.2008.00808.x. Epub 2009 May 19.
Results Reference
background
PubMed Identifier
17443585
Citation
Nonoyama ML, Brooks D, Lacasse Y, Guyatt GH, Goldstein RS. Oxygen therapy during exercise training in chronic obstructive pulmonary disease. Cochrane Database Syst Rev. 2007 Apr 18;2007(2):CD005372. doi: 10.1002/14651858.CD005372.pub2.
Results Reference
background
PubMed Identifier
18718038
Citation
ZuWallack RL. The roles of bronchodilators, supplemental oxygen, and ventilatory assistance in the pulmonary rehabilitation of patients with chronic obstructive pulmonary disease. Respir Care. 2008 Sep;53(9):1190-5.
Results Reference
background
PubMed Identifier
19010994
Citation
Watz H, Waschki B, Meyer T, Magnussen H. Physical activity in patients with COPD. Eur Respir J. 2009 Feb;33(2):262-72. doi: 10.1183/09031936.00024608. Epub 2008 Nov 14. Erratum In: Eur Respir J. 2010 Aug;36(2):462.
Results Reference
background
PubMed Identifier
15860711
Citation
Puhan MA, Schunemann HJ, Frey M, Scharplatz M, Bachmann LM. How should COPD patients exercise during respiratory rehabilitation? Comparison of exercise modalities and intensities to treat skeletal muscle dysfunction. Thorax. 2005 May;60(5):367-75. doi: 10.1136/thx.2004.033274.
Results Reference
background
PubMed Identifier
19321869
Citation
Casaburi R, ZuWallack R. Pulmonary rehabilitation for management of chronic obstructive pulmonary disease. N Engl J Med. 2009 Mar 26;360(13):1329-35. doi: 10.1056/NEJMct0804632. No abstract available.
Results Reference
background
Links:
URL
http://www.nlm.nih.gov/medlineplus/copdchronicobstructivepulmonarydisease.html
Description
Related Info
URL
http://www.salk.at/
Description
Related Info

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SCOPE-Study: Salzburg Chronic Obstructive Pulmonary Disease- Exercise and Oxygen Study

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