Sarah N Miller, Martina Mueller, Michelle Nichols, Ronald J Teufel, Diana M Layne, Charlie Strange, Mohan Madisetti, MaryChris Pittman, Teresa J Kelechi, Paul W Davenport
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The theoretically-informed, technology-enhanced RESP-FIT intervention for COPD is a 6-week combined inspiratory and expiratory muscle strength training program with symptom measurement in real time via ecological momentary assessment (EMA).</p><p><strong>Objectives: </strong>In addition to hypothesis generating purposes, the purpose of this randomized control pilot study was to explore whether observed effects (on symptoms, patient-reported outcomes, and respiratory muscle strength) support carrying out a future large-scale trial of RESP-FIT.</p><p><strong>Methods: </strong>Thirty adults with COPD were randomized to intervention (n=15) or control, with intervention group undergoing 6 weeks of mHealth-enhanced RMST. Daily symptom data were collected in real time over the 6-week intervention period using EMA.</p><p><strong>Results: </strong>Compared to the control group, participants in the intervention group reported decreased dyspnea and anxiety, increased happiness, and improved respiratory muscle strength (PIMax). However, reports of fatigue and sleep disturbance increased in the intervention group compared to the control group.</p><p><strong>Conclusion: </strong>Results support the hypothesis that the 6-week RESP-FIT program will improve respiratory muscle strength, emotional state (anxiety and happiness), and breathlessness in COPD but may contribute to fatigue, at least in the short-term. Future work is needed to determine efficacy of RESP-FIT, determine mechanisms of action on dyspnea and fatigue, and conduct within-subject comparisons of EMA data to explore individual or environmental fluctuations in COPD symptoms.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"RESP-FIT: A Technology-Enhanced Combined Inspiratory and Expiratory Muscle Strength Training Intervention for Adults With COPD.\",\"authors\":\"Sarah N Miller, Martina Mueller, Michelle Nichols, Ronald J Teufel, Diana M Layne, Charlie Strange, Mohan Madisetti, MaryChris Pittman, Teresa J Kelechi, Paul W Davenport\",\"doi\":\"10.15326/jcopdf.2024.0523\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Chronic obstructive pulmonary disease (COPD) is a progressive respiratory disease associated with respiratory muscle weakness and activity-limiting symptoms such as dyspnea. Respiratory muscle strength training (RMST) is an empirically validated therapy to increase respiratory muscle strength. The theoretically-informed, technology-enhanced RESP-FIT intervention for COPD is a 6-week combined inspiratory and expiratory muscle strength training program with symptom measurement in real time via ecological momentary assessment (EMA).</p><p><strong>Objectives: </strong>In addition to hypothesis generating purposes, the purpose of this randomized control pilot study was to explore whether observed effects (on symptoms, patient-reported outcomes, and respiratory muscle strength) support carrying out a future large-scale trial of RESP-FIT.</p><p><strong>Methods: </strong>Thirty adults with COPD were randomized to intervention (n=15) or control, with intervention group undergoing 6 weeks of mHealth-enhanced RMST. Daily symptom data were collected in real time over the 6-week intervention period using EMA.</p><p><strong>Results: </strong>Compared to the control group, participants in the intervention group reported decreased dyspnea and anxiety, increased happiness, and improved respiratory muscle strength (PIMax). However, reports of fatigue and sleep disturbance increased in the intervention group compared to the control group.</p><p><strong>Conclusion: </strong>Results support the hypothesis that the 6-week RESP-FIT program will improve respiratory muscle strength, emotional state (anxiety and happiness), and breathlessness in COPD but may contribute to fatigue, at least in the short-term. 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引用次数: 0
摘要
背景:慢性阻塞性肺疾病(COPD)是一种进行性呼吸系统疾病,伴有呼吸肌无力和活动受限症状,如呼吸困难。呼吸肌力量训练(RMST)是一种经过经验验证的增强呼吸肌力量的疗法。针对慢性阻塞性肺病的RESP-FIT疗法是一项为期6周的吸气和呼气肌力综合训练计划,并通过生态瞬间评估(EMA)对症状进行实时测量:除了提出假设外,这项随机对照试验研究的目的还在于探索观察到的效果(对症状、患者报告结果和呼吸肌力量的影响)是否支持未来对 RESP-FIT 进行大规模试验:30名慢性阻塞性肺病成人患者被随机分为干预组(15人)和对照组,干预组接受为期6周的移动医疗增强型RMST治疗。在为期 6 周的干预期间,使用 EMA 实时收集每日症状数据:结果:与对照组相比,干预组的参与者报告呼吸困难和焦虑减少了,幸福感增加了,呼吸肌强度(PIMax)提高了。然而,与对照组相比,干预组的疲劳和睡眠障碍报告有所增加:结果支持以下假设:为期 6 周的 RESP-FIT 计划将改善慢性阻塞性肺病患者的呼吸肌力量、情绪状态(焦虑和快乐)和呼吸困难,但至少在短期内可能会导致疲劳。未来的工作需要确定 RESP-FIT 的疗效,确定其对呼吸困难和疲劳的作用机制,并对 EMA 数据进行受试者内比较,以探索 COPD 症状的个体或环境波动。
RESP-FIT: A Technology-Enhanced Combined Inspiratory and Expiratory Muscle Strength Training Intervention for Adults With COPD.
Background: Chronic obstructive pulmonary disease (COPD) is a progressive respiratory disease associated with respiratory muscle weakness and activity-limiting symptoms such as dyspnea. Respiratory muscle strength training (RMST) is an empirically validated therapy to increase respiratory muscle strength. The theoretically-informed, technology-enhanced RESP-FIT intervention for COPD is a 6-week combined inspiratory and expiratory muscle strength training program with symptom measurement in real time via ecological momentary assessment (EMA).
Objectives: In addition to hypothesis generating purposes, the purpose of this randomized control pilot study was to explore whether observed effects (on symptoms, patient-reported outcomes, and respiratory muscle strength) support carrying out a future large-scale trial of RESP-FIT.
Methods: Thirty adults with COPD were randomized to intervention (n=15) or control, with intervention group undergoing 6 weeks of mHealth-enhanced RMST. Daily symptom data were collected in real time over the 6-week intervention period using EMA.
Results: Compared to the control group, participants in the intervention group reported decreased dyspnea and anxiety, increased happiness, and improved respiratory muscle strength (PIMax). However, reports of fatigue and sleep disturbance increased in the intervention group compared to the control group.
Conclusion: Results support the hypothesis that the 6-week RESP-FIT program will improve respiratory muscle strength, emotional state (anxiety and happiness), and breathlessness in COPD but may contribute to fatigue, at least in the short-term. Future work is needed to determine efficacy of RESP-FIT, determine mechanisms of action on dyspnea and fatigue, and conduct within-subject comparisons of EMA data to explore individual or environmental fluctuations in COPD symptoms.