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Clinical Trials/NCT07634757
NCT07634757Not yet recruitingNot Applicable

Mobile Geriatric Unit (MGU) to Reduce Hospitalisations in Nursing Home Residents: A Prospective Observational Before-After Study

Universität des Saarlandes1 site in 1 country4,907 target enrollmentStarted: September 1, 2026Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
4,907
Locations
1

Study Overview

Brief Summary

This prospective observational before-after study evaluates the impact of a Mobile Geriatric Unit (MGU) on hospitalisation rates among nursing home residents. The study includes a 12-month control phase with usual care followed by a 12-month intervention phase during which the MGU is implemented. The MGU provides advanced on-site diagnostics and telemedicine-supported specialist consultation within nursing homes.

Detailed Description

This prospective observational before-after study evaluates the impact of a Mobile Geriatric Unit (MGU) on hospitalisation rates among nursing home residents in Saarland, Germany. The study includes a 12-month control phase with usual care followed by a 12-month intervention phase with MGU implementation in 46 nursing homes.

The MGU provides on-site advanced diagnostics (CT, X-ray, ultrasound, ECG, EEG, and laboratory testing) supported by telemedicine consultation with hospital specialists. A physician and radiology technician perform diagnostics in the nursing home, with results communicated to the general practitioner for treatment decisions within 48 hours.

Usual care involves hospital referral and in-hospital diagnostics. The intervention aims to reduce avoidable hospital admissions by providing diagnostics and specialist input directly in the nursing home.

The primary outcome is hospital admissions per person-year. Secondary outcomes include mortality, functional and cognitive status, quality of life (EQ-5D-5L), complications, healthcare costs, and 30-day hospitalisation-free survival.

Eligible participants are nursing home residents with consent or proxy consent; those requiring immediate hospitalisation are excluded.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Residents of participating nursing homes
  • Informed consent from participant or legal representative

Exclusion Criteria

  • Acute life-threatening conditions requiring immediate hospitalisation

Arms & Interventions

Control Phase (Usual Care)

Usual care including general practitioner (GP) referral, hospital transport, and in-hospital diagnostics and treatment.

Intervention Phase (MGU)

On-site diagnostic evaluation using the Mobile Geriatric Unit with broad diagnostic capabilities followed by teleconsultation and further treatment by the general practitioner.

Intervention: Mobile Geriatric Unit (MGU) (Other)

Outcomes

Primary Outcomes

Not specified

Secondary Outcomes

  • Quality of life (EQ-5D-5L)(Day 180)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Klaus Faßbender

Principal Investigator

Universität des Saarlandes

Study Sites (1)

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