跳至主要内容
临床试验/DRKS00040923
DRKS00040923进行中(未招募)不适用

Assessing the Effect of reducing Pulmonary Rehabilitation Group Training weeks from 13 to 7 on the 6-min Walking Test Outcomes in COPD Patients: A retrospective Cohort Study

Stadtspital Zürich0 个研究点目标入组 80 人开始时间: 2026年6月9日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
80

研究概览

简要总结

This study showed that a 7- week PR group training programme, following 9 one- on one coaching and introduction sessions, is non- inferior to a 13- week group training programme relating to results in the 6 Minutes Walk Test (6MWT). Non- Inferiority Analysis Using ANCOVA analyses of the 6MWT times showed that test results at the end of pulmonary rehabilitation (PR) were strongly and significantly associated with results in the baseline test (F=80.2, p: >0.001) and no significant difference between endpoints in both cohorts (F=0.019, p= 0.89). Mean (95%CI) values of the 6MWT results at the end of the programme were 423.9 (394.3 – 453.5) in cohort 1 and 421.2 (396.3 – 446.1) meters in cohort 2. Pairwise comparison of cohort 1 to 2 showed a non- significant mean difference (95%CI) of -2.7 (-36.5 – 41.8) meters. Individual Efficacy of the Programmes Within-group analyses by paired t- test of cohort 1 (13 weeks) (N=15) showed a 6MWT mean (standard error, SE) of 416.2 (29.1) meters before PR and 445.1 (28.4) after, resulting in a non- significant mean clinical difference (95% CI) of 28.9 (-1.1 – 58.9) (p=0.058) meters. Cohort 2’s (7 weeks) paired t- test (N=21) showed a 6MWT mean (SE) of 371.6 (21.5) meters before PR and 406.0 (20.8) after, resulting in a significant mean clinical difference (95% CI) of 34.4 (6.8 – 61.9) (p=0.017) meters. As cohort 2 reached the MCID of 30 meters, 7 weeks of PR are enough to elicit meaningful change in patients when looking at exercise capacity. And while the small sample size and design of the evaluated programme limited comparability, the author cautiously suggests that the 13- week programme would probably have reached the MCID as well, if a larger sample was studied.

研究设计

研究类型
Observational

入排标准

性别
All

入选标准

  • Attended the whole pulmonary rehabilitation programme
  • Took a 6MWT at the beginning and end of the programme.
  • Signed the general consent of the municipal Hospital Zurich or the study-specific consent form.
  • Have a diagnosis of COPD

排除标准

  • Did not sign a consent form
  • Had an interruption in attendance of the PR for more than 2 weeks.
  • Are diagnosed with significant cardiovascular disease limiting the performance in PR and/or 6MWT, defined as training restriction by physician’s orders or inability to train beyond BORG 3/
  • This limits the usual endurance-training intensity to BORG 6/10 in COPD patients and can lead to underachievement in terms of improvement
  • Showed sign of significant musculoskeletal disease limitation in 6MWT, defined as: performance limited by pain, as this is an external limiting factor, unrelated to COPD.

研究者

发起方
Stadtspital Zürich

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