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Clinical Trials/NCT02114879
NCT02114879CompletedNot Applicable

Enhanced Medical Rehabilitation in Older Adults

Washington University School of Medicine3 sites in 1 country229 target enrollmentStarted: July 29, 2014Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
229
Locations
3
Primary Endpoint
Change in Barthel Index Score

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
65 Years to — (Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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.

Arms & Interventions

Standard of Care Rehabilitation

Active Comparator

Intervention: Standard of Care Rehabilitation (Behavioral)

Enhanced Medical Rehabilitation

Experimental

Intervention: Enhanced Medical Rehabilitation (Behavioral)

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

  • 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)
  • Discharge Disposition(Discharge, an average of 24 days after baseline.)
  • 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)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Eric Lenze

Professor of Psychiatry

Washington University School of Medicine

Study Sites (3)

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