New EU study aims to boost resilience in millions of unpaid caregivers
NCT ID NCT07708649
First seen Jul 16, 2026 · Last updated Jul 17, 2026 · Updated 1 time
Summary
This study tests digital education and peer-support programs designed to improve resilience and mental wellbeing in informal carers and long-term care workers. Researchers will roll out these programs in five European countries and measure their effects on mental health and care partnerships. The goal is to identify practices that can be adopted across different healthcare systems to better support those who care for others.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- digital educational program and peer-to-peer support program
- What this could lead to
- If successful, this could point toward scalable ways to improve mental wellbeing and resilience among the millions of unpaid caregivers and long-term care workers across Europe.
- What could go wrong
- This is an implementation study, not a controlled drug trial, so results may vary by local context and may not be generalizable. The interventions are still being developed, and the study does not test a single standardized treatment.
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
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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
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About 450 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2027
An estimate. Start dates often move.
- Expected to finish
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Sep 2027
An estimate. End dates often move.
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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.
Inclusion criteria for recruiting participants will be... For informal caregivers: o currently providing - or having provided within the last 6 months - unpaid care or support to a family member, partner, or friend receiving long-term care services; For long-term care workers: * employed in a long-term care setting at one of the participating research sites; * directly involved in care provision or implementation of the new practices under study; For care recipients: * currently receiving care from long-term care workers and/or informal caregivers; * requiring support with everyday personal care and/or more complex daily tasks due to ageing, chronic illness, disability or frailty; * living in the community or in a long-term care setting included in the study; \- for other stakeholders: * involved directly or indirectly in the planning, management, or implementation of the newly adopted practices at the research site; For all participants: * aged 18 years or older; * able to provide informed consent; * sufficient proficiency in the local language to complete the questionnaire and/or participate in an interview; The exclusion criteria for recruiting participants will be... * having a (permanent or temporary) psychiatric disorder or mental illness which makes the person unable to understand instructions and participate in the study activities; * experiencing circumstances that would make participation unduly burdensome (e.g., acute stress or illness); * providing care for fewer than the minimum number of hours required for inclusion; the threshold will be defined per country in a context-sensitive way, reflecting national differences and the characteristics of the implemented practices and their target populations; * only being involved in the provision or receiving of short-term or acute care (i.e., not long-term care);
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
5 sites in 5 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hochschule Zittau/Görlitz
Zittau, Germany
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INRCA
Ancona, Italy
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Linneaus University
Kalmar, Sweden
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University of Ljubljana
Ljubljana, Slovenia
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Vrije Universiteit Amsterdam
Amsterdam, Netherlands
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