Clinical trial registry record

Deprescribing for Older Adults After Hospital Discharge in Home Health Care

A registered study indexed because it matched monitored longevity research terms. Registry status: Completed. Registration does not establish safety or effectiveness.

Plain-language guide

Five questions to ask about this record

What this is
A clinical study registration, not a result or recommendation.
Why it may matter
The registry currently reports Completed.
Evidence
Registered phase not reported study.
Main limitation
Registration does not prove that the intervention works, is safe, or is available to you.
What changed
Registry metadata was last updated July 16, 2025.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT05630144
Last registry update
July 16, 2025
Status
Completed
Phase
Phase not reported
Sponsor
University of Rochester
Enrollment
5
Countries
United States
Match confidence
80%
Source feed
ClinicalTrials.gov
Automated source synopsis

A registered study indexed because it matched monitored longevity research terms. Registry status: Completed. Registration does not establish safety or effectiveness.

Evidence snapshot

What the source actually supports

Evidence stage
Phase not reported
Study design
NA · SINGLE GROUP · TREATMENT · NONE
Evidence population
Human clinical study registration
Participants
5
Population
ALL · 65 Years
Duration
2023-03-29 to 2025-05-30
Intervention
HomeMed
Comparator
Not reported
Outcomes measured
mean time spent on intervention — 3 months; number of participants who complete a post intervention survey about feasibility — 3 months; Percentage of participants undergoing deprescribing — 3 months; Percentage of intervention adherence indicators checked — 3 months; Percentage of patients who improve in ability to do things that are important before and after intervention — 3 months; Total number of medications used per participant — 3 months; Percentage of patients who report a reduction in medication burden — 3 months; Percentage of participants who report a reduction in medication side effect — 3 months
Reported result
No reusable finding-level result is available in this record.

Main limitationThis is a study registration. No reusable structured result is available here, so it cannot show whether the intervention worked or was safe.

Safety and approvalEligibility, adverse-event details, and clinical decisions must be checked in the official registry and with qualified clinicians. Trial registration is not regulatory approval and does not establish that an intervention is available.

Source supportStructured registry protocol metadata; no finding-level conclusion is generated.

Trial stage · Phase not reportedA trial phase describes development stage; it does not establish a positive result.
Phase 1Phase 2Phase 3Phase 4

Registration and recruitment status do not establish safety, efficacy, or regulatory approval.

Why this record appears here · 80% topic match

The title, summary, or source keywords matched one or more topics followed by immortal.life. A higher percentage means a stronger topic match; it does not rate safety, effectiveness, or study quality.

  • Deprescribing · 80%Title contains controlled topic terminology. Title supplies ageing or longevity context.

Automated source check 100% · update recency 65%. These figures help sort records; they are not medical ratings.

deprescribing
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