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Deprescribing for Older Adults After Hospital Discharge in Home Health Care

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University of Rochester

Status

Completed

Conditions

Polypharmacy

Treatments

Behavioral: HomeMed

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05630144
R24AG064025 (U.S. NIH Grant/Contract)
STUDY00007846

Details and patient eligibility

About

The purpose of this study is to examine the feasibility of providing a medication optimization program to improve patient health outcomes during the transition from hospital to home. This is because the period after hospital discharge is critical to long-term recovery, overall quality of life, and prevention of future hospitalizations.

Enrollment

5 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Patient Inclusion Criteria:

  • 65 years of age and older
  • currently hospitalized or having been hospitalized in the previous 2 weeks
  • having a discharge disposition of home with a referral to receive HHC services from URMHC, or currently receiving HHC services from URMHC
  • taking more than 10 regular medications daily
  • having a primary care provider who is in the URMC system
  • Ability to self-consent
  • English-speaking

Patient Exclusion Criteria:

  • end-of-life prognosis in the following 6 months
  • currently receiving hospice care, end-of-life care, or palliative care
  • conditions that impact the receipt of the intervention, such as severe cognitive impairment that interferes with the subject's ability to communicate with interventionists;
  • substantial difficulties in hearing, vision, and verbal expression that disable the participant from communicating effectively while receiving the HomeMed intervention

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

5 participants in 1 patient group

All Participants
Experimental group
Treatment:
Behavioral: HomeMed

Trial contacts and locations

1

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Central trial contact

Jinjiao Wang, PhD

Data sourced from clinicaltrials.gov

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