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Clinical Trials/NCT02114879
NCT02114879
Completed
N/A

Enhanced Medical Rehabilitation in Older Adults

Washington University School of Medicine3 sites in 1 country229 target enrollmentJuly 29, 2014

Overview

Phase
N/A
Intervention
Not specified
Conditions
Disabling Medical Events
Sponsor
Washington University School of Medicine
Enrollment
229
Locations
3
Primary Endpoint
Change in Barthel Index Score
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study is to provide evidence that Enhanced Medical Rehabilitation is an effective treatment for older adults after disabling medical events.

Detailed Description

The intervention involves physical and occupational therapy for patients who have been admitted to a skilled nursing facility for therapy following a disabling medical event. Participants in this study will be randomly assigned to receive either Enhanced or standard of care therapy, meaning they will either receive their PT (Physical Therapy)\& OT(Occupational Therapy) from therapists who have been specially trained in the study intervention or from therapists with normal training. Participants will be assessed at baseline, 30, 60, and 90 days after baseline, and at the date of their discharge from the skilled nursing facility.

Registry
clinicaltrials.gov
Start Date
July 29, 2014
End Date
July 13, 2018
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Eric Lenze

Professor of Psychiatry

Washington University School of Medicine

Eligibility Criteria

Inclusion Criteria

  • 65 and older
  • Admitted to a skilled nursing facility for post-acute care from PT and OT for 2 weeks or more.

Exclusion Criteria

  • Language, visual or hearing barriers to participation
  • Medical illness preventing study participation or accurate data collection
  • Moderate-severe dementia (demonstrated by chart diagnosis and/or short blessed score greater than 13)
  • Progressive neurological condition such that recovery of function is not feasible
  • Patient did not have the ability to walk prior to hospitalization (e.g. paraplegic)
  • Schizophrenia or other chronic or current psychotic disorder.

Outcomes

Primary Outcomes

Change in Barthel Index Score

Time Frame: Baseline and Discharge, an average of 24 days.

Barthel Index scores range from 0 to 100, with higher scores indicating greater levels of function.

Secondary Outcomes

  • Discharge Disposition(Discharge, an average of 24 days after baseline.)
  • Gait Speed (Determined by 4 or 10 Meter Walk Test)(Discharge, an average of 24 days after baseline.)
  • Self-reported Barthel Index(30, 60, and 90 Days Post Admission to the SNF)
  • Distance Ambulated in 6-Minute Walk Test(Discharge, an average of 24 days after baseline.)
  • Rehospitalizations(Days 30, 60, and 90 post admission to a SNF as well as at Discharge)

Study Sites (3)

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