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New Decision-Support tool aims to ease suffering for palliative care patients

NCT ID NCT06107946

What the study statuses mean

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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
Running, but no longer taking on new participants.
Completed This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This pilot study tested a clinical decision-support system called MuSt-PC, designed to help doctors and nurses manage multiple symptoms in patients receiving palliative care. 44 adults with life-limiting illnesses and at least two moderate-to-severe symptoms participated. The study focused on whether patients could complete the required questionnaires and how well they followed the system's advice.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
clinical decision support system (MuSt-PC)
What this could lead to
If successful, this tool could help doctors better manage multiple symptoms in palliative care, potentially improving patients' quality of life.
What could go wrong
This is a very small pilot study (44 patients) focused on feasibility, not effectiveness. The tool may not work in larger or more diverse groups.

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

44 people

The number who actually took part.

Started

Apr 2024

Finished

Feb 2025

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

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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.

Inclusion Criteria: * Patients identified as in a palliative care trajectory (based on a negative answer to the surprise question "Would I be surprised if this patiënt died in the next 12 months?") * All primary diseases (cancer, non-cancer (e.g. COPD, haart failure, frailty) * Patients should have at least two symptoms on the Utrecht Symptom Diary with a numeric rating score of 4 or higher * Life expectancy of at least 4 weeks * Able to fill out Dutch questionnaires * Informed consent Exclusion Criteria: * Patients who are unable or unwilling to self-assess their symptoms at baseline.

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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

  • LUMC

    Leiden, Netherlands

  • University Medical Center Groningen

    Groningen, Netherlands

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