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Clinical Trials in China / NCT07612072
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Elastic-Band Resistance and Breathing Training for Older Adults With Pulmonary Function Impairment

NCT07612072 · tracked via the Priya Life Science China tracker
Sponsor
Beijing Sport University
Phase
Not applicable
Started
2026-06-10
Last updated
2026-07-02

Condition(s) studied

Respiration Disorders

Investigational drug(s) / intervention(s)

Elastic-Band Resistance Training Plus Breathing TrainingElastic-Band Resistance Training

Elastic-Band Resistance Training Plus Breathing Training: Supervised elastic-band resistance training plus structured breathing training is provided for 12 weeks in a community health service setting. Participants attend 3-5 supervised sessions per week, with at least 3 sessions weekly. Each session includes approximately 60 minutes of elastic-band resistance training, consisting of warm-up, progressive exercises for the upper limbs, lower limbs, and trunk, and cool-down. Intensity is monitored using the OMNI-RES scale and adjusted according to movement quality and tolerance. An additional 10-minute breathing module includes inspiratory and expiratory trainer exercises, diaphragmatic breathing, pursed-lip breathing, rhythmic breathing, and breathing control. Participants also complete about 10 minutes of home-based breathing exercises on non-supervised days. Usual health education is provided.

Elastic-Band Resistance Training: Supervised elastic-band resistance training is provided for 12 weeks in a community health service setting. Participants attend 3-5 supervised sessions per week, with at least 3 sessions weekly. Each session lasts approximately 60 minutes and includes a warm-up, progressive elastic-band resistance exercises targeting the upper limbs, lower limbs, and trunk, and a cool-down. Training intensity is monitored using the OMNI-RES scale and adjusted according to movement quality and participant tolerance. Usual health education is also provided. No structured breathing training or home-based breathing exercises are included.

Study summary

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

Eligibility

Sex
ALL
Min age
60 Years
Max age
85 Years
Healthy volunteers
No
Inclusion Criteria: * Age 60 to 85 years * Pulmonary function impairment identified by community-based spirometry screening * Community-dwelling older adults * Able to communicate and walk independently * Willing to participate in the 12-week intervention and all study assessments * Provided written informed consent Exclusion Criteria: * Acute or unstable cardiovascular, respiratory, or severe musculoskeletal disease that made exercise training unsafe * Recent acute exacerbation, surgery, severe infection, or other health event that could affect safe participation * Significant cognitive impairment, communication disorder, or inability to cooperate with training or assessments * Currently receiving systematic pulmonary rehabilitation or regular structured exercise training that could affect the intervention effect * Unable to meet spirometry quality-control requirements * Unable to complete key baseline outcome assessments

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Huayuan Road Community Health Service Center, Haidian District, Beijing Beijing Beijing Municipality

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07612072 on ClinicalTrials.gov ↗ ← All trials in China