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Elastic-Band Resistance and Breathing Training for Older Adults With Pulmonary Function Impairment

Study acronym: EBBT-PFI
StatusCompleted
PhaseNot applicable
Started
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Record History

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  1. Notable Primary endpoints: details revised at 1 of 3 entries Show 5 more changesShow less
    • Completed without a posted recruiting period
    • Final enrollment: 90 participants (planned 75)
    • Eligibility criteria expanded, about 12 words
    • Secondary endpoints: details revised at 12 of 13 entries
    • Site contact updated
  2. Notable Primary endpoint(s) modified
    • Secondary endpoints: 9 to 13
    v3
  3. Minor Eligibility criteria revisedv2
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this clinical trial is to learn whether elastic-band resistance training, with or without breathing training, can improve lung function and physical function in older adults with pulmonary function impairment living in the community. It will also learn about the safety and feasibility of these exercise programs. The main questions it aims to answer are: Does elastic-band resistance training improve lung function, lower-limb muscle strength, walking ability, and exercise tolerance? Does adding structured breathing training to elastic-band resistance training provide additional benefits for lung function and respiratory-related health status? Are these exercise programs safe and acceptable for older adults in a community setting? Researchers will compare three groups: elastic-band resistance training plus breathing training, elastic-band resistance training alone, and usual health education. This will help determine whether elastic-band resistance training is helpful and whether breathing training adds extra benefit. Participants will: Take part in a 12-week study Be assigned by chance to one of three groups Attend supervised exercise sessions 3 times per week if assigned to an exercise group Receive usual health education and daily activity guidance Complete lung function tests, muscle strength tests, physical function tests, and questionnaires at the start of the study, at 6 weeks, and at 12 weeks
Trial Details
NCT Number NCT07612072
Lead Sponsor Beijing Sport University
Conditions
(from sponsor)
Respiration Disorders
Related terms Respiration Disorders
Enrollment 90 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov