Life sciences · Interventional Study
ClinicalTrials.gov · October 7, 2026
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Interventional Study.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
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Registry record from ClinicalTrials.gov (NCT07862738). This is a study registration, not published results. Lead sponsor: NYU Langone Health. Recruitment status: NOT_YET_RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 30 participants (ESTIMATED). Conditions: Heart Failure, Heart Failure New York Heart Association Class III, Heart Failure New York Heart Association Class IV. Interventions: DEVICE: POWERbreathe KH2; OTHER: Usual Care. Primary outcome measures: Percentage of completed training session , Final Visit (up to 6 months); Time required to administer and monitor IMT sessions , Final Visit (up to 6 months); Number of left ventricular assist device (LVAD) implantation or heart transplantation , Final Visit (up to 6 months). Brief summary: The primary objective of this study is to evaluate the feasibility and safety of inspiratory muscle training (IMT) when implemented as part of routine inpatient physical therapy care in patients undergoing evaluation for advanced heart therapies. The secondary aim is to determine if IMT improves 6-minute walk test (6MWT), dyspnea, Maximal Inspiratory Pressure (MIP) pre-operatively. Thirdly, to determine if IMT decreases ICU and hospital length of stay post-operatively.