NCT07015112

Brief Summary

The goal of this clinical trial is to learn if a multi-professional (conducted by geriatricians, clinical pharmacists, nurses) medication revision, centered on patients' goals and characteristics, can improve treatment adequacy in older adults admitted to an intermediate care hospital. The main question it aims to answer is: does this approach reduce the average number of medications taken per patient? Researchers will compare this multi-professional patient-centered revision to the usual standard of care (treatment revision conducted by a clinical pharmacist) to see if the patient-centered revision works in improving treatment adequacy. Participants admitted to an intermediate care hospital will undergo a comprehensive assessment by a geriatrician, and a medication revision (conducted by a multidisciplinary team or a clinical-pharmacist alone). They will also be asked to fulfill some questionnaires on their health status and attitudes. Any possible adverse events to the medications will be recorded at discharge. Participants will be contacted again three months after discharge to check for any readmission or death.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
300

participants targeted

Target at P75+ for not_applicable

Timeline
1mo left

Started Jan 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress97%
Jan 2024Jun 2026

Study Start

First participant enrolled

January 4, 2024

Completed
1.4 years until next milestone

First Submitted

Initial submission to the registry

June 1, 2025

Completed
10 days until next milestone

First Posted

Study publicly available on registry

June 11, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2025

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Expected
Last Updated

June 11, 2025

Status Verified

June 1, 2025

Enrollment Period

1.9 years

First QC Date

June 1, 2025

Last Update Submit

June 10, 2025

Conditions

Keywords

polypharmacyfrailtyadverse drug eventdeprescribing

Outcome Measures

Primary Outcomes (1)

  • Number of drugs

    Median number of drugs per patient

    Baseline and after discharge, an average of 30 days

Study Arms (2)

Control (usual care)

NO INTERVENTION

Control arm will receive usual standard of care

Intervention (patient-centered medication review)

EXPERIMENTAL

Intervention arm will receive a multidisciplinary patient-centered medication review

Other: Patient-centered multidisciplinary treatment review

Interventions

Patient-centered multidisciplinary treatment review is defined as a medication review conducted by a multidisciplinary team (geriatrician, clinical pharmacist, nurse) according to a patient-centered methodology, based on person-centered evaluation of both personal and clinical insights, diagnostic-centered evaluation (based on current guidelines), and drug-centered evaluation (based on adequacy)

Intervention (patient-centered medication review)

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)

You may qualify if:

  • older adults (65+ years)
  • ≥ 3 or more chronic conditions requiring medical therapy
  • able to speak Spanish
  • capacity to provide informed consent or have a surrogate able to consent on their behalf

You may not qualify if:

  • unable to provide informed consent
  • anticipated length of hospital stay \< 72h
  • estimated life expectancy \< 3 months
  • homeless
  • already enrolled in a drug trial

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Parc Sanitari Pere Virgili

Barcelona, Barcelona, 08023, Spain

RECRUITING

MeSH Terms

Conditions

FrailtyDrug-Related Side Effects and Adverse Reactions

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and SymptomsChemically-Induced Disorders

Central Study Contacts

Ana M de Andrés Lázaro, Pharmacist. PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Stepped-wedge
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 1, 2025

First Posted

June 11, 2025

Study Start

January 4, 2024

Primary Completion

December 1, 2025

Study Completion (Estimated)

June 1, 2026

Last Updated

June 11, 2025

Record last verified: 2025-06

Locations