Comparison of Community Reintegration Interventions When Using a Simulated Environment (NCT06646939) | Clinical Trial Compass
TerminatedNot Applicable
Comparison of Community Reintegration Interventions When Using a Simulated Environment
Stopped: Low accrual
United States13 participantsStarted 2023-07-05
Plain-language summary
The investigators believe that rehabilitation specialists will use community reintegration treatments more if a simulated environment is available.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Medical records of patients admitted to the IRU from January 1, 2015 through December 31, 2019 will be queried for number of minutes billed for Community Integration.
* Medical records of patients admitted to the IRU from April 2
* Patients admitted to the Inpatient Rehabilitation Unit (IRU) of at least 18 years of age and older
* Patients who can read and provide informed consent in English.
* Patients who will be discharged to home after inpatient rehabilitation.
* Patients who are ambulatory with a minimal QI score of 3 on "Walk 10 feet".
* Patients who utilized the simulated environment during their inpatient stay.
* Patients who score 8 or greater on the BIMS on initial evaluation.
Exclusion Criteria:
* The investigators will exclude medical records of patients admitted to the IRU from January 1, 2020 through December 31, 2021 because of the COVID restrictions that were in place.
* Patients who are less than 18 years of age.
* Patients who are not ambulatory due to medical reasons.
* Patients who cannot read and provide informed consent in English.
* Patients who were discharged to acute care, skilled nursing facility or long-term care facility after their inpatient rehabilitation stay.
* Patients who did not use the simulated environment during their inpatient stay.
* Patients who score 7 or lower on the BIMS on initial evaluation.
What they're measuring
1
Utilization of community reintegration, as measured by number of 15-minute units billed
Timeframe: Duration of IRU stay, an average of 11 days
Trial details
NCT IDNCT06646939
SponsorWeill Medical College of Cornell University