Wu 2017.
Study characteristics | ||
Methods |
Study design: RCT Study grouping: parallel‐group |
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Participants |
Baseline characteristics IMT (Threshold device)
IMT (resistive device)
Control/sham
Overall
Included criteria
Excluded criteria
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Interventions |
Intervention characteristics IMT: participants trained twice a day, 15 min/session for 8 weeks using either Threshold IMT (Respironics Inc; Pittsburgh, PA, USA) or Pflex (Respironics Inc, Pittsburgh, PA, USA) devices set at 60% of PImax Control/sham: no intervention received by this group |
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Outcomes | Dyspnea: BDI‐TDI
Functional exercise capacity:
HRQoL: CRQ
Respiratory muscle strength: PImax (RV) Laboratory exercise test: VO2peak (L/min) (Incremental cycle ergometer test) Respiratory function: FEV1
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Identification |
Sponsorship source: the study was supported by the Science and Technology Project of Guangdong Province (2017A020211018) and the Guangzhou Healthcare collaborative innovation major project (201604040012) and State's Key Project of Research and Development Plan(2017YFSF11078). Country: China Setting: Guangzhou Institute of Respiratory Disease Author's name: Rongchang Chen Institution: Guangzhou Institute of Respiratory Disease, State Key Laboratory of Respiratory Disease Email: chenrc_vip@163.com Address: Guangzhou, China Clinical trial register: NCT03101774 |
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Notes |