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A Geriatric Mobile Team for Nursing Home Residents: a Feasibility Pilot Study

A Geriatric Mobile Team for Nursing Home Residents: an Exploratory, Prospective, Single-Center, Non-Randomized, Non-Interventional Feasibility Pilot Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06873919
Acronym
GerMoT
Enrollment
200
Registered
2025-03-13
Start date
2025-03-05
Completion date
2026-02-28
Last updated
2025-03-13

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

Conditions

Geriatric Assessment, Nursing Home Resident

Brief summary

Nursing home (NH) residents have complex healthcare needs. Barriers to collaboration hinder the delivery of high-quality care in nursing homes. To bridge the gap between hospital-based and NH-based care, various innovative approaches have been proposed, including geriatric mobile teams. In Belgium, geriatric expertise has long been confined to hospital settings. Until recently, no specific organization existed for outpatient geriatric assessment, particularly for NH residents. In April 2024, the National Institute for Health and Disability Insurance (INAMI) introduced a new reimbursement code for geriatric consultations in NHs, promoting the development of extramural geriatric activities. However, evidence on the effectiveness of mobile geriatric teams remains limited, particularly regarding hospitalization prevention. The geriatrics department of CHU UCL Namur is implementing a one-year pilot project involving a mobile team composed of a geriatrician and a nurse to conduct geriatric assessments in the three nursing homes. This non-randomized pilot project aims to establish a new standard of care for residents selected by their general practitioner, leveraging the new reimbursement code. The project is accompanied by a clinical study assessing the feasibility, effectiveness, and acceptability of this intervention. Prospectively collected data will also help define key indicators for a future large-scale study focused on cost-effectiveness.

Interventions

OTHERGeriatric assessment

The tertiary hospital's geriatrics department is implementing a one-year mobile team composed of a geriatrician and a nurse to conduct geriatric assessments (Anamnesis and heteroanamnesis - Clinical examination - Medication review - Proposed management plan provided to the general practionner, who independently decides which recommendations to implement) in three nursing homes. This non-randomized pilot project aims to establish a new standard of care for residents selected by their primary care physician. The project is accompanied by a clinical study designed to assess the feasibility, effectiveness, and acceptability of this intervention. Prospectively collected data will also help define key indicators for a future large-scale study focusing on cost-effectiveness.

Sponsors

CHU UCL Namur
CollaboratorUNKNOWN
Université Catholique de Louvain
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Patients aged over 70 years * Presenting with one or more of the following conditions: * Difficulties in establishing an advance care planning * Medical complexity (multiple specialists, repeated hospitalizations) * Polypharmacy * Recurrent falls * Unmanageable behavioral disorders * Weight loss * Memory impairment

Exclusion criteria

* Patients with an unstable medical condition requiring urgent care * Patients under 70 years old * Patients whose condition requires examinations or treatments available only in a hospital setting

Design outcomes

Primary

MeasureTime frame
FeasabilityImmediately after the initial consultation, with follow-up assessments at 3, 6, 9, and up to 12 months post-inclusion.

Secondary

MeasureTime frame
AcceptabilityImmediately after the initial consultation, with follow-up assessments at 3, 6, 9, and up to 12 months post-inclusion
Determine the outcomes for a future full evaluation study.Immediately after the initial consultation, with follow-up assessments at 3, 6, 9, and up to 12 months post-inclusion

Countries

Belgium

Contacts

Primary ContactMarie de Saint-Hubert
marie.desainthubert@chuuclnamur.uclouvain.be+3281424027

Outcome results

None listed

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