Frailty, Rehabilitation, Transcatheter Aortic Valve Replacement
Conditions
Brief summary
The PREPARE TAVR pilot study will examine the effects of remotely administered physiological reconditioning program (RAPR) on quality of life (QOL) and clinical outcomes at one year post TAVR in frail older adults.
Detailed description
The main objective of this study is to evaluate the effects of a home based exercise and dietary intervention program on the quality of life (QOL) and clinical outcomes in frail adults undergoing Transcatheter aortic valve replacement (TAVR) procedures. Patients will be randomly (1:1) assigned to the standard of care (SOC group) where patients will receive all medical care as decided by their treating physicians or assigned to a home based program known as remotely administered physiological reconditioning (RPR) program which will include receiving personalized instructions for a progressive exercise program and dietary changes. Patients will be contacted for regular phone and in-person follow up for monitoring their progress. The primary endpoint will be quality of life as assessed by KCCQE questionnaires at one-year post TAVR. The secondary endpoints include length of stay post TAVR, all-cause mortality, repeat hospitalization and a composite of all-cause mortality and repeat hospitalization at one year.
Interventions
OTHERRemotely administered physiological reconditioning program
Patients assigned to intervention arm will be provided a personalized, tailored and graduated exercise program to improve physical strength and conditioning.
Sponsors
Unity Health Toronto
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Masking description
The outcomes assessed in a blinded manner
Intervention model description
Prospective, multicenter, randomized trial with objective end points assessment
Eligibility
Sex/Gender
ALL
Age
60 Years to 95 Years
Healthy volunteers
No
Inclusion criteria
\- Short Physical Performance Battery Protocol (SPPB) score \< 9
Exclusion criteria
* Severe liver disease defined by Childs Pugh class \>B or MELD score \>15. * Severe kidney disease defined by eGFR \<30 mL/min. * Hospital admission during the 4 weeks prior to randomization. * Montreal objective cognitive assessment (MOCA) score \<18. * Mechanical fall in the past month. * Unstable angina during the previous month. * Myocardial infarction during the previous month. * Unsuccessful completion of the one-week run-in phase. * Syncopal episode during exercise during run-in phase
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Quality of Life (QOL) | One year | Quality of life as assessed by the Kansas City Cardiomyopathy Questionnaire (KCCQ). KCCQE is a 23-item self-administered questionnaire developed to independently measure the patient's perception of their health status, which includes heart failure symptoms, impact on physical and social function, and how their heart failure impacts their quality of life (QOL) within a 2-week recall period. KCCQ responses are provided along a rating scale continuum with equal spacing from worst to best. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| LOS | Index hospitalization | Length of stay post TAVR |
| MACE | one year | Composite of mortality and repeat hospitalization |
Countries
Canada
Contacts
Primary ContactSyed Ishba
Outcome results
None listed