RECRUITING

Comparison of Community Reintegration Interventions When Using a Simulated Environment

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Simulated Environments for Community ReintegrationInpatient Rehabilitation UnitCommunity ReintegrationSimulated Environment

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The investigators believe that rehabilitation specialists will use community reintegration treatments more if a simulated environment is available.

Official Title

Comparison of Community Reintegration Interventions Relative to the Institution of a Simulated Environment in Inpatient Rehabilitation and Pilot Study of the Impact of Simulated Environment on Functional Outcomes

Quick Facts

Study Start:2023-07-05
Study Completion:2025-07-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06646939

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 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.
  2. * Medical records of patients admitted to the IRU from April 2
  3. * Patients admitted to the Inpatient Rehabilitation Unit (IRU) of at least 18 years of age and older
  4. * Patients who can read and provide informed consent in English.
  5. * Patients who will be discharged to home after inpatient rehabilitation.
  6. * Patients who are ambulatory with a minimal QI score of 3 on "Walk 10 feet".
  7. * Patients who utilized the simulated environment during their inpatient stay.
  8. * Patients who score 8 or greater on the BIMS on initial evaluation.
  1. * 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.
  2. * Patients who are less than 18 years of age.
  3. * Patients who are not ambulatory due to medical reasons.
  4. * Patients who cannot read and provide informed consent in English.
  5. * Patients who were discharged to acute care, skilled nursing facility or long-term care facility after their inpatient rehabilitation stay.
  6. * Patients who did not use the simulated environment during their inpatient stay.
  7. * Patients who score 7 or lower on the BIMS on initial evaluation.

Contacts and Locations

Study Contact

Amy Meyer, DPT
CONTACT
646-832-6431
amm9045@nyp.org
Caitlin Burke, DPT
CONTACT
cab9172@nyp.org

Principal Investigator

Nasim Chowdhury, MD
PRINCIPAL_INVESTIGATOR
Weill Medical College of Cornell University

Study Locations (Sites)

NewYork Presbyterian Hospital Baker Pavilion
New York, New York, 10065
United States

Collaborators and Investigators

Sponsor: Weill Medical College of Cornell University

  • Nasim Chowdhury, MD, PRINCIPAL_INVESTIGATOR, Weill Medical College of Cornell University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-07-05
Study Completion Date2025-07-01

Study Record Updates

Study Start Date2023-07-05
Study Completion Date2025-07-01

Terms related to this study

Keywords Provided by Researchers

  • Inpatient Rehabilitation Unit
  • Community Reintegration
  • Simulated Environment

Additional Relevant MeSH Terms

  • Simulated Environments for Community Reintegration