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Elastic-Band Resistance and Breathing Training for Older Adults With Pulmonary Function Impairment (EBBT-PFI)

torstai 28. toukokuuta 2026 päivittänyt: Beijing Sport University

Effects of Elastic-Band Resistance Training With or Without Breathing Exercise on Pulmonary Function and Functional Performance in Community-Dwelling Older Adults With Pulmonary Function Impairment: A Randomized Controlled Trial

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

Tutkimuksen yleiskatsaus

Yksityiskohtainen kuvaus

Detailed Description

Pulmonary function impairment is common in older adults and may be associated with reduced physical activity, lower exercise tolerance, poorer functional performance, and impaired respiratory-related health status. Community-dwelling older adults with early or mild pulmonary function decline may not receive formal pulmonary rehabilitation, but they may still benefit from simple, low-cost, and feasible exercise-based interventions.

This study was designed to evaluate whether a community-based elastic-band resistance training program, with or without structured breathing training, could improve pulmonary function and functional performance in older adults with pulmonary function impairment. Eligible participants were community-dwelling adults aged 60 years or older who were identified through pulmonary function screening. Participants were randomly assigned to one of three groups: elastic-band resistance training plus breathing training, elastic-band resistance training alone, or usual health education.

The elastic-band resistance training program used progressive resistance exercises targeting upper-limb, lower-limb, and trunk-related functional movement patterns. Training intensity was monitored using a perceived exertion scale and adjusted according to each participant's tolerance and movement quality. The structured breathing training program included breathing control exercises and breathing trainer-based practice, with progression based on training level, breath-holding or maintenance time, repetitions, and perceived breathing effort.

The intervention lasted 12 weeks. Participants in the exercise groups attended supervised sessions three times per week in a community health service setting, while the control group received usual health education and daily activity guidance. Study assessments were conducted at baseline, 6 weeks, and 12 weeks to examine changes in pulmonary function, muscle strength, functional performance, respiratory-related health status, sleep quality, adherence, and safety.

This study may provide evidence for a practical community-based exercise approach for older adults with pulmonary function impairment and may help clarify whether adding structured breathing training to elastic-band resistance training provides additional benefits.

Opintotyyppi

Interventio

Ilmoittautuminen (Arvioitu)

75

Vaihe

  • Ei sovellettavissa

Yhteystiedot ja paikat

Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.

Opiskeluyhteys

Opiskelupaikat

    • Beijing Municipality
      • Beijing, Beijing Municipality, Kiina, 100084
        • Huayuan Road Community Health Service Center, Haidian District, Beijing
        • Ottaa yhteyttä:
          • Yan Wang, Doctor
          • Puhelinnumero: +86-15201061266
          • Sähköposti: wyweiwei@126.com

Osallistumiskriteerit

Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.

Kelpoisuusvaatimukset

Opintokelpoiset iät

  • Aikuinen
  • Vanhempi Aikuinen

Hyväksyy terveitä vapaaehtoisia

Ei

Kuvaus

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

Opintosuunnitelma

Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.

Miten tutkimus on suunniteltu?

Suunnittelun yksityiskohdat

  • Ensisijainen käyttötarkoitus: Hoito
  • Jako: Satunnaistettu
  • Inventiomalli: Rinnakkaistehtävä
  • Naamiointi: Yksittäinen

Aseet ja interventiot

Osallistujaryhmä / Arm
Interventio / Hoito
Kokeellinen: Elastic-Band Resistance Training Plus Breathing Training
Participants in this arm received supervised elastic-band resistance training combined with structured breathing training for 12 weeks, in addition to usual health education. The elastic-band resistance training was performed 3 times per week and included warm-up, progressive resistance exercises targeting upper-limb, lower-limb, and trunk-related functional movements, and cool-down. Training intensity was monitored using the OMNI-RES perceived exertion scale and adjusted according to movement quality and participant tolerance. The breathing training included breathing trainer-based practice, diaphragmatic breathing, pursed-lip breathing, rhythmic breathing, and breathing control exercises. Participants also received daily activity guidance and health education.
Supervised elastic-band resistance training plus structured breathing training for 12 weeks. Participants trained 3 times per week in a community health service setting. Resistance training included warm-up, progressive elastic-band exercises, and cool-down, targeting upper-limb, lower-limb, and trunk-related functional movements. Intensity was monitored using the OMNI-RES scale and adjusted according to tolerance and movement quality. Breathing training included breathing trainer practice, diaphragmatic breathing, pursed-lip breathing, rhythmic breathing, and breathing control. Usual health education was also provided.
Supervised elastic-band resistance training for 12 weeks. Participants trained 3 times per week in a community health service setting. Each session included warm-up, progressive elastic-band resistance exercises, and cool-down. Exercises targeted upper-limb, lower-limb, and trunk-related functional movements. Intensity was monitored using the OMNI-RES scale and adjusted according to tolerance and movement quality. Usual health education was also provided. No structured breathing training was provided.
Active Comparator: Elastic-Band Resistance Training
Participants in this arm received supervised elastic-band resistance training for 12 weeks, in addition to usual health education. The training was performed 3 times per week and included warm-up, progressive elastic-band resistance exercises, and cool-down. Exercises targeted upper-limb, lower-limb, and trunk-related functional movement patterns. Training intensity was monitored using the OMNI-RES perceived exertion scale and adjusted according to participant tolerance and movement quality. No structured breathing training was provided in this arm.
Supervised elastic-band resistance training for 12 weeks. Participants trained 3 times per week in a community health service setting. Each session included warm-up, progressive elastic-band resistance exercises, and cool-down. Exercises targeted upper-limb, lower-limb, and trunk-related functional movements. Intensity was monitored using the OMNI-RES scale and adjusted according to tolerance and movement quality. Usual health education was also provided. No structured breathing training was provided.
Ei väliintuloa: Usual Health Education
Participants in this arm did not receive systematic exercise training. They received usual health education and daily activity guidance, including general lifestyle advice, basic physical activity recommendations, and safety instructions. Participants completed the same study assessments at baseline, 6 weeks, and 12 weeks.

Mitä tutkimuksessa mitataan?

Ensisijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Change in FEV1/FVC Ratio From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
The FEV1/FVC ratio was calculated from standardized spirometry results. The change from baseline to Week 12 was used to evaluate airflow limitation. Higher values generally indicate better pulmonary function.
Baseline, Week 6, and Week 12
Change in Forced Expiratory Volume in 1 Second From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
Forced expiratory volume in 1 second (FEV1) was measured using standardized spirometry. The change from baseline to Week 12 was used to evaluate improvement in pulmonary function. Higher values indicate better lung function.
Baseline, Week 6, and Week 12
Change in Forced Vital Capacity From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
Forced vital capacity (FVC) was measured using standardized spirometry. The change from baseline to Week 12 was used to evaluate improvement in pulmonary function. Higher values indicate better lung function.
Baseline, Week 6, and Week 12
Change in FEV1 Z-Score From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
FEV1 z-score was calculated using reference equations to standardize pulmonary function according to age, sex, height, and ethnicity. The change from baseline to Week 12 was used to evaluate standardized improvement in pulmonary function. Higher z-scores indicate better lung function.
Baseline, Week 6, and Week 12
Change in FVC Z-Score From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
FVC z-score was calculated using reference equations to standardize pulmonary function according to age, sex, height, and ethnicity. The change from baseline to Week 12 was used to evaluate standardized improvement in pulmonary function. Higher z-scores indicate better lung function.
Baseline, Week 6, and Week 12
Change in FEV1/FVC Z-Score From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
FEV1/FVC z-score was calculated using reference equations to standardize the ratio according to age, sex, height, and ethnicity. The change from baseline to Week 12 was used to evaluate standardized change in airflow limitation. Higher z-scores indicate better pulmonary function.
Baseline, Week 6, and Week 12
Change in 30-Second Chair Stand Test Performance From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
The 30-second chair stand test was used to assess repeated sit-to-stand ability. Participants were asked to complete as many full sit-to-stand repetitions as possible within 30 seconds. Higher values indicate better lower-limb functional performance.
Baseline, Week 6, and Week 12
Change in 4-Meter Gait Speed From Baseline to Week 12
Aikaikkuna: The 4-meter gait speed test was used to assess usual walking ability. Participants walked a fixed 4-meter distance at their usual comfortable speed. Higher values indicate better walking performance.
Baseline, Week 6, and Week 12
The 4-meter gait speed test was used to assess usual walking ability. Participants walked a fixed 4-meter distance at their usual comfortable speed. Higher values indicate better walking performance.
Change in 2-Minute Step Test Performance From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
The 2-minute step test was used to assess short-duration exercise tolerance. Participants stepped in place for 2 minutes, and the number of valid steps reaching the required knee height was recorded. Higher values indicate better exercise tolerance.
Baseline, Week 6, and Week 12

Toissijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Change in Dominant-Side Quadriceps Strength From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
Dominant-side quadriceps strength was measured using a standardized muscle strength testing device. The change from baseline to Week 12 was used to evaluate lower-limb muscle strength. Higher values indicate greater muscle strength.
Baseline, Week 6, and Week 12
Change in Non-Dominant-Side Quadriceps Strength From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
Non-dominant-side quadriceps strength was measured using a standardized muscle strength testing device. The change from baseline to Week 12 was used to evaluate lower-limb muscle strength. Higher values indicate greater muscle strength.
Baseline, Week 6, and Week 12
Change in Dominant-Side Triceps Surae Strength From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
Dominant-side triceps surae strength was measured using a standardized muscle strength testing device. The change from baseline to Week 12 was used to evaluate lower-limb muscle strength. Higher values indicate greater muscle strength.
Baseline, Week 6, and Week 12
Change in Non-Dominant-Side Triceps Surae Strength From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
Non-dominant-side triceps surae strength was measured using a standardized muscle strength testing device. The change from baseline to Week 12 was used to evaluate lower-limb muscle strength. Higher values indicate greater muscle strength.
Baseline, Week 6, and Week 12
Change in Timed Up and Go Test Performance From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
The Timed Up and Go test was used to assess functional mobility. Participants stood up from a chair, walked a fixed distance, turned around, returned to the chair, and sat down. Shorter completion time indicates better functional mobility.
Baseline, Week 6, and Week 12
Change in Dominant-Side Handgrip Strength From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
Dominant-side handgrip strength was measured using a standardized handgrip dynamometer. The change from baseline to Week 12 was used to evaluate upper-limb and overall muscle strength. Higher values indicate greater muscle strength.
Baseline, Week 6, and Week 12
Change in Non-Dominant-Side Handgrip Strength From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
Non-dominant-side handgrip strength was measured using a standardized handgrip dynamometer. The change from baseline to Week 12 was used to evaluate upper-limb and overall muscle strength. Higher values indicate greater muscle strength.
Baseline, Week 6, and Week 12
Change in St. George's Respiratory Questionnaire Total Score From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
Respiratory-related health status was assessed using the St. George's Respiratory Questionnaire total score. The change from baseline to Week 12 was used to evaluate respiratory symptoms and health-related quality of life. Lower scores indicate better respiratory-related health status.
Baseline, Week 6, and Week 12
Change in Pittsburgh Sleep Quality Index Total Score From Baseline to Week 12
Aikaikkuna: Baseline, Week 6, and Week 12
Sleep quality was assessed using the Pittsburgh Sleep Quality Index total score. The change from baseline to Week 12 was used to evaluate changes in subjective sleep quality. Lower scores indicate better sleep quality.
Baseline, Week 6, and Week 12

Yhteistyökumppanit ja tutkijat

Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.

Opintojen ennätyspäivät

Nämä päivämäärät seuraavat ClinicalTrials.gov-sivustolle lähetettyjen tutkimustietueiden ja yhteenvetojen edistymistä. National Library of Medicine (NLM) tarkistaa tutkimustiedot ja raportoidut tulokset varmistaakseen, että ne täyttävät tietyt laadunvalvontastandardit, ennen kuin ne julkaistaan ​​julkisella verkkosivustolla.

Opi tärkeimmät päivämäärät

Opiskelun aloitus (Arvioitu)

Keskiviikko 10. kesäkuuta 2026

Ensisijainen valmistuminen (Arvioitu)

Tiistai 15. syyskuuta 2026

Opintojen valmistuminen (Arvioitu)

Keskiviikko 16. syyskuuta 2026

Opintoihin ilmoittautumispäivät

Ensimmäinen lähetetty

Torstai 21. toukokuuta 2026

Ensimmäinen toimitettu, joka täytti QC-kriteerit

Torstai 21. toukokuuta 2026

Ensimmäinen Lähetetty (Todellinen)

Torstai 28. toukokuuta 2026

Tutkimustietojen päivitykset

Viimeisin päivitys julkaistu (Todellinen)

Maanantai 1. kesäkuuta 2026

Viimeisin lähetetty päivitys, joka täytti QC-kriteerit

Torstai 28. toukokuuta 2026

Viimeksi vahvistettu

Perjantai 1. toukokuuta 2026

Lisää tietoa

Tähän tutkimukseen liittyvät termit

Yksittäisten osallistujien tietojen suunnitelma (IPD)

Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?

EI

IPD-suunnitelman kuvaus

Individual participant data will not be shared because the study involves health-related data from older adults, and public sharing was not specified in the informed consent or ethics approval. De-identified data may be considered only upon reasonable request and with appropriate ethical approval.

Lääke- ja laitetiedot, tutkimusasiakirjat

Tutkii yhdysvaltalaista FDA sääntelemää lääkevalmistetta

Ei

Tutkii yhdysvaltalaista FDA sääntelemää laitetuotetta

Ei

Nämä tiedot haettiin suoraan verkkosivustolta clinicaltrials.gov ilman muutoksia. Jos sinulla on pyyntöjä muuttaa, poistaa tai päivittää tutkimustietojasi, ota yhteyttä register@clinicaltrials.gov. Heti kun muutos on otettu käyttöön osoitteessa clinicaltrials.gov, se päivitetään automaattisesti myös verkkosivustollemme .

Kliiniset tutkimukset Elastic-Band Resistance Training Plus Breathing Training

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