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Completed

NCT Number: NCT02860728

Resistance Training to Prehabilitate Patients With Chronic Obstructive Pulmonary Disease

Structural changes in skeletal muscles of patients with chronic obstructive pulmonary disease (COPD) have been linked to impaired muscle function, reduced exercise capacity, and increased mortality associated with this disease. Muscle dysfunction also contributes to dyspnea intensity and the ability to sustain exercise, making aerobic exercise training intolerable at the intensity and/or volume required to achieve clinically important changes. Resistance training (RT) is an attractive exercise modality because it is efficacious and more tolerable initially. No work has examined whether a short-term RT program can reduce exertional symptoms and improve exercise tolerance (dyspnea and leg fatigue) in patients with COPD.

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Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of British Columbia

Kelowna, British Columbia, V1V 1V7, Canada

About this study

Skeletal muscle dysfunction is common in patients with COPD and has been recognized as a contributing factor to reduced exercise capacity, health related quality of life and increased mortality associated with this disease. Several structural changes in the limb muscles of patients have previously been reported and have been linked to the known reductions in muscle strength and endurance commonly reported in COPD. Muscle dysfunction, lower extremity muscle strength, and muscle fatigue also contribute to the intensity of dyspnea and the ability to sustain exercise mostly through stimulation of type III and IV muscle afferents. As such, many patients who primarily perform aerobic exercise training as part of pulmonary rehabilitation are unable to tolerate the intensity and/or volume of exercise required to achieve clinically important changes in exercise capacity or symptom relief. Resistance training (RT) is an attractive exercise modality for patients with COPD because it is efficacious and often more tolerable initially. To our knowledge no one has examined whether similar benefits to those elicited by longer RT programs can be attained in just 4 weeks using multi-joint, multi-muscle exercises and individualized progression. If a short term RT program can improve muscle quality, enhance endurance, and reduce type III and IV afferent activity then it would reduce the drive to breathe and thus dyspnea. These adaptations would likely translate into improved exercise tolerance making it feasible to "pre-habilitate" COPD patients with tolerable RT, allowing them to achieve a higher volume/intensity of endurance training, thus making pulmonary rehabilitation more effective.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Non-smokers >6 months
  • FEV1/FVC <0.7 and lower limit of normal
  • 30%< FEV1 pred <70%
  • Stable (no exacerbation for >3 months)

Exclusion criteria

  • Cardiovascular and cerebrovascular disease
  • Diabetes
  • Cardiovascular contraindications to exercise
  • Uncontrolled hypertension
  • Currently performing regular structured exercise >3x/week for 30 minutes

Treatment and study plan

Individualized Resistance Training

Behavioral

Lower body resistance exercises will be prescribed in various combinations over multiple days and individually modified and progressed to achieve advances in both movement pattern, intensity, and exercise volume.

Primary outcomes

  1. Dyspnea

    Time frame: Baseline and post 4 weeks (12 sessions) of resistance training

    The change in the sensory intensity of dyspnea measured at an iso-time during the constant load exercise trials post RT

Secondary outcomes

  1. Exercise Tolerance

    Time frame: Baseline and post 4 weeks (12 sessions) of resistance training

    The change in the time to exhaustion during constant load exercise on a stationary cycle ergometer.

  2. Secondary Dyspnea Outcomes

    Time frame: Baseline and post 4 weeks (12 sessions) of resistance training

    The change in the unpleasantness and sensory qualities of dyspnea measured at an iso-time during the constant load exercise trials post RT

  3. Quadriceps Fatigue

    Time frame: Baseline and post 4 weeks (12 sessions) of resistance training

    Change in the amount of decline in force production after 3 minutes of electrical stimulation of femoral nerve at 25% of maximal voluntary contraction

  4. Muscle Strength and Endurance

    Time frame: Baseline and post 4 weeks (12 sessions) of resistance training

    The change in 6RM quadriceps muscle strength and quadricep muscle endurance at 50% of predicted 1 RM

Sponsors and collaborators

Lead sponsor

University of British Columbia

Other

Registry information

Official study title

A Novel Individualized Resistance Training Program to Prehabilitate Patients With Chronic Obstructive Pulmonary Disease

Important dates

Study start
2016
Primary completion
2020
Study completion
2020
First posted
Aug 9, 2016
Registry last updated
Jun 13, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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