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A Prospective Cohort Study of Clinical and Process Outcomes of Older Adults That Transition Through the Geriatric Emergency Medicine Unit(GEM-U)

A Prospective Cohort Study of the Clinical and Process Outcomes of Older Adults That Transition Through the Geriatric Emergency Medicine Unit (GEM-U)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07237334
Enrollment
150
Registered
2025-11-19
Start date
2025-02-10
Completion date
2026-03-30
Last updated
2025-11-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Frailty

Keywords

Comprehensive Geriatric Assessment

Brief summary

This study will characterise the patients using the Geriatric Emergency Medicine Unit, a unit which provides specialist care for patients aged 75 years and older attending the emergency department. It will examine how this specialist care impacts their health in terms of a number of different outcomes, such as; function, quality of life and health care usage; for example admission to the acute hospital.

Detailed description

The emergency department is a particularly challenging and busy environment, particularly for older adults living with frailty. It is widely acknowledged throughout the literature and national healthcare strategy that these older adults require holistic, person centred care that targets the intricacies of multifaceted, complex health issues. The geriatric emergency medicine unit (GEM-U) aims to provide such care through the framework of comprehensive geriatric assessment, with in-put from a team of healthcare disciplines. The main aim of this study is to look at how this specialist care impacts patient outcomes, such as acute admission. Clinical and process outcomes of participants will be examined using patient reported outcome measures, which will include; 1. Global measure of function (Barthel Index) 2. Delirium screen (4AT +/- Delirium Rating Scale)\* 3. Frailty status (Clinical Frailty Scale) 4. Nutritional status (Mini Nutritional Assesment) 5. Quality of life (EuroQoL-5D-5L). 6. Patient satisfaction (PSQ-18). Participants will be followed at 30 days and 6 months post recruitment. All participants will give fully informed consent. The STrengthening the Reporting of OBservational studies in Epidemiology (STROBE) standardised reporting guidelines will be followed in the conduct and reporting of this research. Data will be statistically analysed

Interventions

None listed

Sponsors

University of Limerick
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
75 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Older adults aged ≥75 years * Manchester Triage System category 2-5 * Screen positive for risk of adverse outcomes after ED visit (≥ 2 on ISAR screening tool) * Presenting with a medical condition * Reviewed by the Older Persons Integrated Care Team

Exclusion criteria

* Patients presenting with a non-medical issue including major trauma or hip fracture * Patients presenting with acute stroke or transient ischaemic attack * Patients more appropriate to another alternative pathway e.g. deep vein thrombosis pathway, low risk chest pain pathway * Patients with acute coronary syndrome or unstable arrthymia * Patients requiring care in the resuscitation room * Patients with head injury (unless appropriate assessment and management has been fully completed by ED team) * Patients with possible spinal injury (unless appropriate assessment and management has been fully completed by ED/orthopaedic team) * Patients with low Glasgow Coma Scale * Other exclusions at the discretion of the Older Persons Integrated Care team depending on team capacity and expertise *

Design outcomes

Primary

MeasureTime frameDescription
Our primary outcome is incidence of hospital admission at index GEM-U presentationPatients are followed at 30 days and 6 monthsPatients who attend GEM-U and have an acute hospital admission at this time

Secondary

MeasureTime frameDescription
MortalityPatients are followed at 30 days and 6 monthsMortality
Unscheduled ED revisitPatients are followed at 30 days and 6 monthsPatients who attend the ED department again during the follow up period
Unscheduled hospital visit(s)Patients are followed at 30 days and 6 monthsPatients who have unplanned hospital admission (i.e. not elective procedure) during follow up period
Nursing home admissionPatients are followed at 30 days and 6 monthsPatients now living in a nursing home
Healthcare utilization (GP visit, out-patient geriatric services, PHN visit, HSCP services)Patients are followed at 30 days and 6 monthsUse of primary care and community care services

Countries

Ireland

Contacts

Primary ContactIda M Carroll, MSc
09006791@studentmail.ul.ie0860638269
Backup ContactRose Galvin
rose.galvin@UL.ie0868463842

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026