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 range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
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