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Clinical Trials/NCT02329873
NCT02329873
Completed
Not Applicable

Efficacy of the Respiratory Rehabilitation Exercise Training Package in Hospitalized Elderly Patients With Acute Exacerbation of Chronic Obstructive Pulmonary Disease: Randomized Control Trial

Chest Hospital, Ministry of Health and Welfare, Taiwan1 site in 1 country61 target enrollmentNovember 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Obstructive Pulmonary Disease (COPD)
Sponsor
Chest Hospital, Ministry of Health and Welfare, Taiwan
Enrollment
61
Locations
1
Primary Endpoint
Change from baseline in dyspnea at 4th day
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this randomized controlled trial was to evaluate the effects of a respiratory rehabilitation exercise training package on dyspnea, cough, exercise tolerance, and sputum expectoration of hospitalized elderly patients with acute exacerbation of chronic obstructive pulmonary disease (AECOPD). Using purposive sampling, 61 participants were recruited and randomly assigned to either the experimental group (n = 30) or the control group (n = 31). The experimental group participants received the respiratory rehabilitation exercise training twice a day and 10-30 minutes per session for four days. The control group participants received usual care and health education. Data were collected at baseline and at the end of the four-day intervention.

Detailed Description

The respiratory rehabilitation exercise training package included: (a) Disease awareness: The doctor explained the disease to patients and their families through the chest X-ray, (b) Sputum clearance treatments: Easily understood postural drainage cards were provided to the patients and families to assist with proper sputum clearance procedures, (c) Pursed lip breathing training: Devices were provided to the patients to ensure that the breathing exercises were completed properly, (d) Upper-limb exercise with breathing pranayama: Towels were provided to the patients to assist with upper-limb exercises properly, (e) Walking training with breathing pranayama: Legs were elevated while inhaling, and returned to the position while exhaling, and (f) Assign a pulmonary rehabilitation program coordinator: Coordinators were assigned to assist the patients in nutrition management and health education.

Registry
clinicaltrials.gov
Start Date
November 2011
End Date
December 2012
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Chest Hospital, Ministry of Health and Welfare, Taiwan
Responsible Party
Principal Investigator
Principal Investigator

Lin-Yu Liao

Head Nurse

Chest Hospital, Ministry of Health and Welfare, Taiwan

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • unstable vital signs
  • blood oxygen concentration lower than 90%
  • unstable psychological status, hemoptysis, pneumothorax, pulmonary edema, or using the respirator

Outcomes

Primary Outcomes

Change from baseline in dyspnea at 4th day

Time Frame: At baseline and at the 4th day of the study

Measured by the Borg Rating of Perceived Exertion Scale.

Secondary Outcomes

  • Change from baseline in cough severity at 4th day(At baseline and at the 4th day of the study)
  • Change from baseline in exercise tolerance at 4th day(At baseline and at the 4th day of the study)
  • Change from baseline in sputum expectoration at 4th day(At baseline and at the 4th day of the study)

Study Sites (1)

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