Can a Nurse-Led program keep nursing home residents out of the hospital?

NCT ID NCT06473051

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at whether a nurse-led care model, called INTERCARE, can be successfully expanded to more nursing homes in Switzerland to reduce unplanned hospital visits for residents. Researchers will work with 40 nursing homes to see how well they follow the program and whether it is cost-effective. The goal is to improve care for older adults while avoiding unnecessary hospital stays.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 40 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jul 2024

Expected to finish

Oct 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

Children (under 18), adults (18 to 64) and older adults (65 and over)

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Study inclusion/exclusion criteria are based on level of participant: 1. LTCF Inclusion criteria: \- Located within German-speaking part of Switzerland \- ≥ 20 long-term care beds on the cantonal list of LTCFs (or a cooperation of smaller LTCFs with a total of at least 20 long-term care beds, working with the same INTERCARE nurse(s)) \- Willingness to introduce the core components of INTERCARE (formal commitment) \- Willingness to provide routine resident assessment data (Resident Assessment Instrument-nursing home version (RAI-NH) or BESA system) Exclusion criteria: \- LTCFs located in the Italian- or French-speaking part of Switzerland. \- LTCFs who have previously worked with a nurse-led model similar to the INTERCARE/INTERSCALE research intervention 2. INTERCARE nurse Inclusion criteria: \- Working contract or affiliation with the LTCF \- Educational background as an RN with ≥ 3 years' experience working with older persons \- Assigned role of INTERCARE nurse Exclusion criteria: \- No contract with the LTCF 3. Other care staff Inclusion criteria: * All care staff who work directly with residents (e.g., care workers, physiotherapists and activity staff) of different educational backgrounds (e.g., RNs, LPNs, nurse aides) working in the LTCF at least 8h/week for ≥ 3 months * Other therapeutic personnel involved in 8h/week or more in treatments/direct contact with residents Exclusion criteria: \- Non-health care professionals (e.g., administration) 4. General Practitioners (GPs) Inclusion criteria: * All GP's who treat at least 5 residents in the LTCF at the time of data collection Exclusion criteria: \- Temporary substitute GPs 5. Residents Inclusion criteria: \- All residents present at the LTCF during the study duration with long-term care and billed according to the health insurance law Exclusion criteria: \- Residents who opt out of participating in the study

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Institute of Nursing Science

    Basel, 4057, Switzerland