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Clinical Trials/NCT04771052
NCT04771052
Completed
Not Applicable

Minimizing the Effects of COVID-19 Hospitalization With the COVID Rehabilitation Program for the Elderly: the CORE Trial in Response to the Pandemic

Université de Sherbrooke2 sites in 1 country124 target enrollmentSeptember 1, 2020
ConditionsCovid19

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Covid19
Sponsor
Université de Sherbrooke
Enrollment
124
Locations
2
Primary Endpoint
Length of stay
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Although evidence from the management of other viral respiratory infections suggest that early multidisciplinary rehabilitation could mitigate the adverse effects of the severe form of the illness, and reduce the length of hospital stays (LOS), specific data for COVID-19 are lacking. Hence, in response to the current pandemic, we propose to implement and assess the impact of an early standardized multidisciplinary rehabilitation program tailored to frail older adults on 1) LOS, 2) post-discharge destination, 3) prognostic index and 4) functional capacity.

With a pragmatic multicenter controlled study, the COvid Rehabilitation Program for the Elderly (CORE) trial will allow to measure the effectiveness of a multidisciplinary program to minimize the effects of hospitalization and provide the required tools to rapidly implement an innovative strategy of care for older adults. Indeed, based on the results of this study, and with the support of scientific and professional organizations, a standardized program tailored to older adults with COVID-19 will be disseminated in Canada for all medical units dedicated to the management of the disease. Because of its pragmatic approach, this study will provide a sustainable multidisciplinary intervention that can be quickly implemented in any Canadian (or abroad) COVID-19 medical unit. Finally, given that COVID-19 is the third coronavirus infection in the last 20 years, the expected results will provide guidelines, with decision tree algorithms, for implementation should another coronavirus or for that matter, any other such type of infection that surface in the future.

Registry
clinicaltrials.gov
Start Date
September 1, 2020
End Date
January 5, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with medical clearance (physical deconditioning; hemodynamically stable; oxygen therapy by nasal cannula \< 4 L/min for saturation \> 92%; resting respiratory rate \< 24; and heart rate between 50 and 120 beats per minute). Controls were paired with those of the CORE program according to age, sex and pre-admission origin

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Length of stay

Time Frame: 1 day after discharge

Length of stay in COVID and subacute unit (days)

Secondary Outcomes

  • Post-discharge destination(1 day after discharge)
  • Readmission rate 30 days after discharge(30 days after discharge)
  • Change in patient prognosis(At baseline (± 2 days after admission in the COVID-19 unit) and before discharge (± 3 days))
  • Change in functional capacity (lower limb function)(At baseline (± 2 days after admission in the COVID-19 unit) and before discharge (± 3 days))
  • Change in functional capacity (handgrip strength)(At baseline (± 2 days after admission in the COVID-19 unit) and before discharge (± 3 days))

Study Sites (2)

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