Comparison of Two Programs to Encourage Physical Activity in Individuals With Chronic Obstructive Pulmonary Disease

Phase 3

Completed

• Conditions: Lung Diseases, Obstructive; Pulmonary Disease, Chronic Obstructive
• Interventions: Behavioral: Lifestyle Activity Program; Behavioral: Exercise Program

• Registration Number: NCT00328484
• Lead Sponsor: National Heart, Lung, and Blood Institute (NHLBI)

Brief Summary

Chronic obstructive pulmonary disease (COPD) is a chronic lung disease. Symptoms include shortness of breath, wheezing, and difficulty exercising. Increasing exercise and physical activity may relieve the symptoms of COPD and may also slow the progression of the disease. The purpose of this study is to evaluate the effectiveness of a lifestyle activity program versus a traditional exercise program at increasing the amount of physical activity among individuals with COPD.

Detailed Description

COPD is a disease in which the lung airways are partly damaged and obstructed, making it difficult to breathe. It is the fourth leading cause of death in the United States. Cigarette smoking is the most common cause of COPD; however, breathing in other types of lung irritants, including pollution, dust, and chemicals, over a long period of time may also cause or contribute to COPD. The primary symptoms of COPD, exercise intolerance and shortness of breath, often result in physical activity limitations, which may lead to a decreased quality of life. While COPD is a chronic, incurable disease, individuals who incorporate exercise and physical activity into their daily lifestyle may reduce the symptoms and slow the progression of the disease. The purpose of this study is to compare the effectiveness of an overall lifestyle activity program versus a traditional exercise program on physical activity in individuals with COPD. The study will also evaluate the impact of the two programs on exercise capacity, physical function, self-reported disability, and health-related quality of life.

Participants with COPD will be randomly assigned to either an 11-month lifestyle activity program or a traditional 3-month exercise program. The lifestyle activity program will consist of 35 exercise and counseling sessions spaced over 11 months. This program will use cognitive-behavioral strategies to encourage physical activity at home. Participants will receive information on how to deal with COPD symptoms (including shortness of breath), goal-setting, social support, and motivation. Participants will also receive follow-up telephone calls from the program staff for additional support. The 3-month exercise program will consist of 36 1-hour exercise training sessions, conducted 3 times a week for 12 weeks.

All participants will attend 4 baseline study visits at which their medical history will be reviewed and standardized questionnaires will be completed to assess mood, depression, social factors, COPD symptoms, and physical activity levels. Participants will undergo a physical examination; a blood draw for laboratory testing; and spirometry, lung function, exercise, and strength tests. These measures will be assessed again at 3, 6, and 12 months; the 3- and 12-month assessments will occur over four study visits, and the 6-month assessment will occur over two study visits.

Study Timeline

• Study Start: 2002-01
• Study First Submitted: 2006-05-19
• Study First Submitted QC: 2006-05-19
• Study First Posted: 2006-05-22
• Primary Completion: 2007-07
• Study Completion: 2007-07
• Status Verified: 2009-02
• Last Update Submitted: 2016-07-28
• Last Update Posted: 2016-07-29

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 318

Inclusion Criteria

• Expiratory airflow limitation such that FEV1/FVC is less than or equal to 70% and the FEV₁ is greater than or equal to 20% of the predicted amount
• Physical disability, including self-reported difficulty with walking a city block, climbing stairs, lifting and carrying groceries, performing household activities such as cleaning and doing yard work, or getting out of a chair
• Currently lives within a 35-mile radius of Wake Forest University
• Plans to reside in Forsyth County, North Carolina for the entire study
• Willing and able to participate in all aspects of the trial

Exclusion Criteria

• Undergoing treatment for cancer
• Severe congestive heart failure
• Stroke
• Peripheral vascular disease
• Coronary artery disease
• Valvular heart disease
• Major psychiatric disease
• Severe anemia
• Liver or kidney disease
• Uncontrolled diabetes or hypertension
• Orthopedic impairment
• Blindness or deafness
• Oxygen desaturation during exercise to less than 90%, at a heart rate less than 50% of predicted maximum for participant's age and without supplemental oxygen
• Inability to exercise due to a physical disability or positive exercise stress test
• Alcohol consumption of greater than two drinks per day in the 2 months prior to study entry

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
1	Lifestyle Activity Program	Eleven month lifestyle activity program
2	Exercise Program	Three month exercise program

Primary Outcome Measures

Name	Time	Method
Amount of time engaged in moderate physical activity each week	Measured at Year 1

Secondary Outcome Measures

Name	Time	Method
Health related quality of life	Measured at Year 1
Self-reported disability	Measured at Year 1
Physical function	Measured at Year 1
Exercise capacity	Measured at Year 1

Trial Locations

Locations (1)

Wake Forest University; 🇺🇸 Winston-Salem, North Carolina, United States