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Walking Program With Pedometer on Quality of Life in COPD

C

Chang Gung University

Status

Completed

Conditions

Chronic Obstructive Pulmonary Disease

Treatments

Other: walking program

Study type

Interventional

Funder types

Other

Identifiers

NCT05251623
TYGH106081

Details and patient eligibility

About

The aim of this study is to investigate the effects of a walking program on exercise capacity and quality of life in patient with COPD. Method: Patients with COPD were randomly assigned to pedometer group (PG) or control group (CON). Subjects in PG walked to target steps daily with pedometer for 6 weeks. Before and after the program, the following measurements were performed: pulmonary function test (PFT), daily steps, Six-Minute Walk Test (6MWT), COPD Assessment Test (CAT), and quality of life questionnaire (SF-12).

Full description

Patients with chronic obstructive pulmonary disease (COPD) are suffered from impaired pulmonary function and dyspnea which result to limited level of physical activity, and impaired quality of life. Exercise and regular physical activity have been proven to break the vicious circle. The aim of this study is to investigate the effects of a walking program on exercise capacity and quality of life in patient with COPD. Method: Patients with COPD were randomly assigned to pedometer group (PG) or control group (CON). Subjects in PG walked to target steps daily with pedometer for 6 weeks. Before and after the program, the pulmonary function was assessed by spiromtery test. The exercise capacity were assessed by six-minute walking test, the physical activity level was assessed by daily steps, The quality of life was assessed by COPD Assessment Test (CAT), and quality of life questionnaire (SF-12).

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Enrollment

45 patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. diagnosed with COPD
  2. in a medically stable condition
  3. able to walk unassisted
  4. ≥ 40 years of age

Exclusion criteria

  1. oxygen therapy,
  2. hemodynamic instability,
  3. signs/symptoms of acute infection
  4. severe neurological, musculoskeletal, or cardiovascular conditions that affect walking

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

45 participants in 2 patient groups

pedometer
Experimental group
Description:
walking with pedometer
Treatment:
Other: walking program
control
No Intervention group
Description:
no intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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