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Single Limb Resistance Training in Patients With Chronic Obstructive Pulmonary Disease (COPD) (COPD)

Primary Purpose

Pulmonary Disease, Chronic Obstructive

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Control group
High-repetitive single limb training
Sponsored by
Umeå University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pulmonary Disease, Chronic Obstructive focused on measuring Pulmonary Disease, Chronic Obstructive, Lung Diseases, Obstructive, Single Limb, Elastic Resistance, Resistance Training, Minor Muscle Mass, Local muscle training

Eligibility Criteria

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

Inclusion Criteria:

  1. Adults 40 years and above.
  2. Stable (no exacerbations within 4 weeks before start of baseline testing) moderate to very severe COPD, stage II-IV, according to GOLD criteria i.e. Forced expiratory volume in one second (FEV1)/ forced vital capacity (FVC) < 0.70, FEV1 < 80% predicted.
  3. Ex-smoker.
  4. Stable medical treatment (no changes < 4 weeks before start of baseline testing).
  5. Living less than 60 km from training facility.

Exclusion Criteria:

  1. Musculoskeletal, rheumatic, cardiac or neurological disorders that might affect the exercise performance in training and tests.
  2. Previous lung surgery.
  3. Acute exacerbations of COPD that require a change in pharmacological management within four weeks preceding the start of the intervention
  4. Long-term oxygen treatment.
  5. Participated in organized exercise training, > 2 times a week, within 6 months before start of intervention.
  6. Body mass index (BMI) < 18 kg/m2.

Sites / Locations

  • Huddinge University Hospital
  • Umeå University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Control group

High-repetitive single limb training

Arm Description

The control group will receive standardized patient education four times, once every two weeks, during the eight week intervention period.

The experimental group will receive a high-repetitive single limb exercise regime, three times a week for two months. In addition, the exercise group will receive patient education at four occasions during the intervention period.

Outcomes

Primary Outcome Measures

Quality of life
The Swedish Self-Administered Standardized version of the Chronic Respiratory Disease Questionnaire (CRQ-SAS) will be used as primary outcome measure to asses quality of life
Functional lower extremity muscular endurance
To asses muscular endurance in the lower extremity the 6-minute walk test will be used as primary outcome measure.
Upper extremity muscular endurance
The 6-minute ring and pegboard test will be used as primary outcome measure for upper extremity muscular endurance

Secondary Outcome Measures

Isokinetic maximal muscle strength
Maximal muscle strength in both upper and lower extremity will be evaluated with an isokinetic dynamometer
Upper extremity muscular endurance
The Unsupported Upper Limb Exercise test will be used as secondary outcome measure for upper extremtiy muscular endurance
Isokinetic muscular endurance capacity
Endurance capacity in both upper and lower extremity will be evaluated with an isokinetic dynamometer
Self-efficacy
Self-efficacy will be evaluated with the exercise self-efficacy scale, and the self-efficacy for walking questionnaire
Anxiety and Depression
Anxiety and Depression will be evaluated with the hospital anxiety and depression scale (HADs)
Relationship between muscle fatigue and dyspnea in the different exercise tests
Muscle fatigue and dyspnea will be measured using the BORG CR10 scale during all exercise tests before the start of the study and on completion 8 weeks later. The relationship between ratings of muscle fatigue between tests, dyspnea between tests and the relationship between muscle fatigue rating and dyspnea rating between exercise tests will be investigated.
Develop a strategy to optimize resistance for each involved movement within an exercise regimen
The exercises used within the intervention group is performed with elastic resistance. How much the elastic band is stretched for the different exercises is determined by a literature search investigation the strenght relationship between the muscles/movements used in the study. During the study each participant in the intervention group will rate muscle fatigue and dyspnea after each exercise during alla exercise sessions. These rating will be used to develop a strategy to optimize resistance for each involved movement within an exercise regimen
Develop a strategy to minimize attempts needed to determine a multiple repetition resistance using elastic bands
55% of the isokinetic peak value obtained during baseline tests will be used to anticipate the 25RM load when using elastic resistance in an attempt to minimize the attempts needed to achieve 25RM.
Determine if this exercise regimen is feasible and safe in stage II-IV COPD patients
Feasibility will be evaluated through number of participants attendance, adherence and number of participants developing any side effects or injuries during each training session. In addition, compliance to the different parts of the exercise regimen will be evaluated with a standardized questionnaire by both study participants and physiotherapists leading interventions.
Identify if there are any sex related differences in exercise training effects
Statistical analyzes will be used to identify if there are any sex related differences in exercise training effects between male and female patients with COPD
Quality-of-life
The clinical COPD questionnaire (CCQ) and the SF-36 scale will be used as secondary outcome measures for Quality-of-life
Exercise capacity
A constant work rate test investigating the effects on endurance time, ventilatory response, perceived dyspnea and leg fatigue during submaximal cycle test.

Full Information

First Posted
May 11, 2011
Last Updated
June 19, 2012
Sponsor
Umeå University
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1. Study Identification

Unique Protocol Identification Number
NCT01354067
Brief Title
Single Limb Resistance Training in Patients With Chronic Obstructive Pulmonary Disease (COPD)
Acronym
COPD
Official Title
Effects of High-repetitive Single Limb Training on Exercise Capacity and Quality of Life in Patients With COPD Compared to a Control Group - A Prospective, Single Blind, Randomized Controlled Multicenter Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2012
Overall Recruitment Status
Completed
Study Start Date
May 2011 (undefined)
Primary Completion Date
May 2012 (Actual)
Study Completion Date
June 2012 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The chronic airflow limitation in chronic obstructive pulmonary disease (COPD) patients resulting in increased dyspnea during physical activity restricts many COPD patients ability to perform exercises in general and whole-body exercises in particular. Single limb training performed as one-legged cycling has been shown effective in patients with COPD. This exercise regime results in less stress on the ventilatory system as training is executed using a simultaneously smaller muscle mass. However, the positive physiological effects of exercise training only occur in the involved muscle(s). To be of benefit for patients daily life, all relevant muscles should be included in exercise training. The aim of the current randomized controlled multicenter trial (RCT) is to determine the effects of high-repetitive single limb exercises (HRSLE) in combination with COPD specific patient education, compared to the COPD specific patient education alone in patients with moderate to very severe (stage II-IV) COPD.
Detailed Description
Chronic obstructive pulmonary disease (COPD) is a major cause of chronic morbidity and mortality in the world. It is one of our most common chronic diseases and up to 700.000 people is estimated to suffer from COPD in Sweden. Exercise intolerance is the key disabling factor in COPD, with decreased exercise capacity, leg fatigue and dyspnea among the most frequently reported symptoms. Different training modalities have been evaluated to uncover the most effective way of training patients with COPD. Traditionally research has used whole-body, or major muscle mass training regimes when investigating the effect of both endurance and resistance in COPD patients. However recent research have demonstrated positive effects using training regimes involving a simultaneous smaller muscle mass compared to traditional exercise. The concept of using this regime is to put less stress on the ventilator system when exercising to minimize the effect of the chronic airflow limitation and to enhance the ability to be able to exercise for this group of patients compared to traditional training using major muscle mass exercise regimes. Although recent research have shown positive effects of single limb training using one-legged cycling, one major limitation is that only a small amount of important muscles for COPD patients are incorporated. Therefore, the aim of this study is to: (i) examine the effect of a single limb exercise regime on local muscle endurance, maximal strength, quality of life, dyspnea, walking capacity, self-efficacy, anxiety and depression, (ii) to examine if the physiological effects differ between man and women and (iii) to investigate if this exercise regime is feasible and safe to use for patients with COPD. Patients diagnosed with moderate to very severe COPD according to GOLD criteria will be randomly assigned to constitute either an exercise or control group The exercise group will participate in a high-repetitive single limb exercise regime, consisting of upper and lower limb exercises with elastic resistance, compromised of three sessions per week over a period of 8 weeks. The exercise regime will be performed in group at Umeå University Hospital of Northern Sweden, and at Huddinge University Hospital, Sweden supervised by experienced physiotherapists. Both the exercise and control group will receive four sessions of standardized patient education during the 8 week intervention period. After completion of the study, patients in the control group will be offered participation in the single limb exercise regime. The most important upper and lower extremity muscles for COPD patients are identified and exercises are designed specific to each of these. The exercise regime consists of 8 exercises, 4 upper extremity and 4 lower extremity exercises. Starting position and performance of the exercises are standardized and the resistance individually adjusted and progressed according to rated dyspnea and muscle fatigue. Before and after the 8 week intervention period the following information will be collected. Effects on maximal strength, muscular endurance, dyspnea, self-efficacy, anxiety and depression. The relationship between changes in health related variables and changes in exercise capacity, sex related differences in training effects, feasibility of the program, strategies to determine adequate starting resistance and provide accurate resistance for each involved movement and the relationship between muscle fatigue and dyspnea in the different exercise tests will also be analyzed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Disease, Chronic Obstructive
Keywords
Pulmonary Disease, Chronic Obstructive, Lung Diseases, Obstructive, Single Limb, Elastic Resistance, Resistance Training, Minor Muscle Mass, Local muscle training

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
44 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control group
Arm Type
Active Comparator
Arm Description
The control group will receive standardized patient education four times, once every two weeks, during the eight week intervention period.
Arm Title
High-repetitive single limb training
Arm Type
Experimental
Arm Description
The experimental group will receive a high-repetitive single limb exercise regime, three times a week for two months. In addition, the exercise group will receive patient education at four occasions during the intervention period.
Intervention Type
Behavioral
Intervention Name(s)
Control group
Intervention Description
The control group receives standardized patient education four times, once every two weeks, during the eight week intervention period. Each session will last 60 minutes, consisting of information regarding anatomy, physiology, causes and mechanisms of COPD, drugs, nutrition, aids and energy saving procedures. The information is the same as for the intervention group, given at separate occasions.
Intervention Type
Behavioral
Intervention Name(s)
High-repetitive single limb training
Intervention Description
The high-repetitive single limb exercise regime consists of three sessions per week during eight weeks of exercise training, giving a total number of 24 sessions at each location (Umeå and Huddinge University hospitals). The exercise sessions are supervised and conducted by a physical therapist using a group format, six to eight participants in each group. Each session will span for 60 minutes, duration of the major components are: 10 min warm-up followed by 40 minutes of single limb training and 10min cool-down. In addition this experimental group also receives four sessions of patient education once every two week.
Primary Outcome Measure Information:
Title
Quality of life
Description
The Swedish Self-Administered Standardized version of the Chronic Respiratory Disease Questionnaire (CRQ-SAS) will be used as primary outcome measure to asses quality of life
Time Frame
Before single limb exercise regime and on completion (at 8 weeks)
Title
Functional lower extremity muscular endurance
Description
To asses muscular endurance in the lower extremity the 6-minute walk test will be used as primary outcome measure.
Time Frame
Before single limb exercise regime and on completion (at 8 weeks)
Title
Upper extremity muscular endurance
Description
The 6-minute ring and pegboard test will be used as primary outcome measure for upper extremity muscular endurance
Time Frame
Before single limb exercise regime and on completion (at 8 weeks)
Secondary Outcome Measure Information:
Title
Isokinetic maximal muscle strength
Description
Maximal muscle strength in both upper and lower extremity will be evaluated with an isokinetic dynamometer
Time Frame
Before single limb exercise regime and on completion (at 8 weeks)
Title
Upper extremity muscular endurance
Description
The Unsupported Upper Limb Exercise test will be used as secondary outcome measure for upper extremtiy muscular endurance
Time Frame
Before single limb exercise regime and on completion (at 8 weeks)
Title
Isokinetic muscular endurance capacity
Description
Endurance capacity in both upper and lower extremity will be evaluated with an isokinetic dynamometer
Time Frame
Before single limb exercise regime and on completion (at 8 weeks)
Title
Self-efficacy
Description
Self-efficacy will be evaluated with the exercise self-efficacy scale, and the self-efficacy for walking questionnaire
Time Frame
Before single limb exercise regime and on completion (at 8 weeks)
Title
Anxiety and Depression
Description
Anxiety and Depression will be evaluated with the hospital anxiety and depression scale (HADs)
Time Frame
Before single limb exercise regime and on completion (at 8 weeks)
Title
Relationship between muscle fatigue and dyspnea in the different exercise tests
Description
Muscle fatigue and dyspnea will be measured using the BORG CR10 scale during all exercise tests before the start of the study and on completion 8 weeks later. The relationship between ratings of muscle fatigue between tests, dyspnea between tests and the relationship between muscle fatigue rating and dyspnea rating between exercise tests will be investigated.
Time Frame
Before single limb exercise regime and on completion (at 8 weeks)
Title
Develop a strategy to optimize resistance for each involved movement within an exercise regimen
Description
The exercises used within the intervention group is performed with elastic resistance. How much the elastic band is stretched for the different exercises is determined by a literature search investigation the strenght relationship between the muscles/movements used in the study. During the study each participant in the intervention group will rate muscle fatigue and dyspnea after each exercise during alla exercise sessions. These rating will be used to develop a strategy to optimize resistance for each involved movement within an exercise regimen
Time Frame
Before single limb exercise regime and on completion (at 8 weeks)
Title
Develop a strategy to minimize attempts needed to determine a multiple repetition resistance using elastic bands
Description
55% of the isokinetic peak value obtained during baseline tests will be used to anticipate the 25RM load when using elastic resistance in an attempt to minimize the attempts needed to achieve 25RM.
Time Frame
Before single limb exercise regime and on completion (at 8 weeks)
Title
Determine if this exercise regimen is feasible and safe in stage II-IV COPD patients
Description
Feasibility will be evaluated through number of participants attendance, adherence and number of participants developing any side effects or injuries during each training session. In addition, compliance to the different parts of the exercise regimen will be evaluated with a standardized questionnaire by both study participants and physiotherapists leading interventions.
Time Frame
Before single limb exercise regime and on completion (at 8 weeks)
Title
Identify if there are any sex related differences in exercise training effects
Description
Statistical analyzes will be used to identify if there are any sex related differences in exercise training effects between male and female patients with COPD
Time Frame
Before single limb exercise regime and on completion (at 8 weeks)
Title
Quality-of-life
Description
The clinical COPD questionnaire (CCQ) and the SF-36 scale will be used as secondary outcome measures for Quality-of-life
Time Frame
Before single limb exercise regime and on completion (at 8 weeks)
Title
Exercise capacity
Description
A constant work rate test investigating the effects on endurance time, ventilatory response, perceived dyspnea and leg fatigue during submaximal cycle test.
Time Frame
Before single limb exercise regime and on completion (at 8 weeks)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults 40 years and above. Stable (no exacerbations within 4 weeks before start of baseline testing) moderate to very severe COPD, stage II-IV, according to GOLD criteria i.e. Forced expiratory volume in one second (FEV1)/ forced vital capacity (FVC) < 0.70, FEV1 < 80% predicted. Ex-smoker. Stable medical treatment (no changes < 4 weeks before start of baseline testing). Living less than 60 km from training facility. Exclusion Criteria: Musculoskeletal, rheumatic, cardiac or neurological disorders that might affect the exercise performance in training and tests. Previous lung surgery. Acute exacerbations of COPD that require a change in pharmacological management within four weeks preceding the start of the intervention Long-term oxygen treatment. Participated in organized exercise training, > 2 times a week, within 6 months before start of intervention. Body mass index (BMI) < 18 kg/m2.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karin Wadell, Ph.D
Organizational Affiliation
Umeå University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Andre Nyberg, Msc
Organizational Affiliation
Umeå University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Britta Lindström, Ph.D
Organizational Affiliation
Umeå University
Official's Role
Study Chair
Facility Information:
Facility Name
Huddinge University Hospital
City
Huddinge
ZIP/Postal Code
141 59
Country
Sweden
Facility Name
Umeå University Hospital
City
Umeå
ZIP/Postal Code
90187
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
22823966
Citation
Nyberg A, Lindstrom B, Wadell K. Assessing the effect of high-repetitive single limb exercises (HRSLE) on exercise capacity and quality of life in patients with chronic obstructive pulmonary disease (COPD): study protocol for randomized controlled trial. Trials. 2012 Jul 23;13:114. doi: 10.1186/1745-6215-13-114.
Results Reference
derived

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Single Limb Resistance Training in Patients With Chronic Obstructive Pulmonary Disease (COPD)

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