New tool aims to ease burden on caregivers of terminally ill patients
NCT ID NCT07193433
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This pilot study tests a tool called CSNAT-I that helps healthcare workers identify and address the needs of family caregivers looking after palliative cancer patients at home. Sixty caregivers in Hong Kong will be randomly assigned to receive the tool or usual care. The study will measure whether the tool reduces caregiver burden and distress, and whether it is practical to use in real-world settings.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Carer Support Needs Assessment Tool Intervention (CSNAT-I)
- What this could lead to
- If it works, this could provide a simple, structured way for healthcare workers to better support family caregivers, reducing their stress and improving their quality of life.
- What could go wrong
- This is a very small pilot study (60 participants) testing feasibility, not a large trial. The tool may not show clear benefits or may be difficult to implement in daily practice.
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 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2025
An estimate. Start dates often move.
- Expected to finish
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May 2026
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 * adults ≥18 years old; * family members taking a primary role in patient care at home as nominated by the palliative cancer patient; * ability to communicate in Chinese. Exclusion Criteria: * paid caregivers; * unable to complete the questionnaire due to mental impairment determined by physicians.
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Genom att skicka in godkänner du våra Användarvillkor
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 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.
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