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Clinical Trials/NCT02979353
NCT02979353
Completed
N/A

A Randomized Controlled Trial to Deprescribe for Older Patients With Polypharmacy Transferred From the Hospital to Skilled Nursing Facilities

Vanderbilt University Medical Center1 site in 1 country372 target enrollmentMarch 6, 2017

Overview

Phase
N/A
Intervention
Not specified
Conditions
Polypharmacy
Sponsor
Vanderbilt University Medical Center
Enrollment
372
Locations
1
Primary Endpoint
Total Number of Medications
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

This randomized, controlled trial will evaluate the effects of an intervention to reduce exposure to medications among hospitalized older adults discharged to skilled nursing facilities (SNFs). The goal of the intervention is to safely deprescribe medications, as defined by dose reductions and stopped medications, based on a combination of clinical criteria and patient preferences. The investigators will evaluate the effects of the intervention on the total number of medications prescribed to patients at hospital and SNF discharge and at home 90-days after SNF discharge along with the prevalence of eight geriatric syndromes, medication adherence, and health status.

Detailed Description

This randomized, controlled trial will evaluate the effects of an intervention to reduce exposure to medications among hospitalized older adults discharged to skilled nursing facilities (SNFs). This study will be conducted in one university-affiliated hospital and 14 area SNFs to enroll approximately 1,300 total participants across five project years. Patients discharged to SNF represent the largest segment of Medicare beneficiaries discharged to post-acute care services and are a particularly high risk group for loss of independence and other poor clinical outcomes. This investigative team recently completed a Centers for Medicare and Medicaid Services (CMS) Innovation Award, which provides strong preliminary data related to the prevalence of polypharmacy and the relationship between polypharmacy and geriatric syndromes (e.g., medications associated with falls) in this patient population. Based on these data, the investigators developed a structured deprescribing intervention protocol ("Shed-Meds") coupled with standardized screening assessments for eight geriatric syndromes to be implemented in the hospital and continued during the SNF stay. The goal of the intervention is to safely deprescribe medications, as defined by dose reductions and stopped medications, based on a combination of clinical criteria and patient preferences. This trial will evaluate the effects of this intervention on medication exposure, medication adherence, geriatric syndromes, and health status across the care transitions from hospital to SNF to home to include a 90-day follow-up period after SNF discharge. The overarching hypothesis is that reducing medications for older patients across the continuum of care will favorably impact geriatric syndromes.

Registry
clinicaltrials.gov
Start Date
March 6, 2017
End Date
May 1, 2021
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sandra Simmons

Principal Investigator

Vanderbilt University Medical Center

Eligibility Criteria

Inclusion Criteria

  • Hospitalized at Vanderbilt University Medical Center
  • Medicare-eligible
  • Discharged from VUMC to a post acute care facility
  • Has polypharmacy as defined by \> 5 medications
  • Able to self-consent or has a proxy (surrogate)
  • Speaks English (due to interview-based assessments)
  • Primary home residence within one of 9 surrounding counties (due to home visit during follow-up phase)

Exclusion Criteria

  • Resides in long-term care
  • Is currently on hospice or otherwise has a limited life expectancy (\< 6 months).
  • Enrolled in a clinical drug trial
  • Has Stage IV Cancer Diagnosis
  • Incarcerated or homeless
  • Unable to self-consent and does not have a surrogate

Outcomes

Primary Outcomes

Total Number of Medications

Time Frame: Hospital Discharge, Post-Acute Care Discharge, and 90 days after discharge from the PAC

The number of medications a participant is taking. This includes all prescribed and over-the-counter medications and both scheduled and as-needed (PRN) medications.

Secondary Outcomes

  • Total Drug Burden Index (DBI): Anticholinergic and Sedative Drug(Hospital Discharge, Post-Acute Care Discharge, and 90 days after discharge from PAC)

Study Sites (1)

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