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Completed

NCT Number: NCT06107946

The MuSt-PC: a Pilot Study to Assess Symptom Burden of Co-occuring Symptoms

In this pilot study, physicians and nurse practitioners working in different care settings will use MuSt-PC, for adult patients with any life-limiting iilness, for whom the Surprise question is answered negatively: if the HCP answers "no" to the question "Would I be surprised if this patiënt died in the next 12 months?''. In total, at least 20 eligible patients will be recruited and asked to perform all study assessments.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Medical Center Groningen, Groningen, Netherlands

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About this study

In this pilot study, physicians and nurse practitioners working in different care settings will use MuSt-PC, for adult patients with any life-limiting iilness, for whom the Surprise question is answered negatively: if the HCP answers "no" to the question "Would I be surprised if this patiënt died in the next 12 months?''. In total, at least 20 eligible patients will be recruited and asked to perform all study assessments.

After a baseline screening assessment, all eligible patients with at least 2 simultaneously occurring symptoms with a numeric rating score £4 on the 11 point scale on the Utrecht Symptom Diary, will be asked to fiil out the Utrecht Symptom Diary during two weeks.

In the first week twice daily (morning and evening), in the second week once daily (evening).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

USD questionnaire

Other

After a baseline screening symptom assessment, all eligible patients with at least 2 simultaneously occurring symptoms with a numeric rating score ≥4 on the 11 point scale on the Utrecht Symptom Diary, will be asked to fill out the Utrecht Symptom Diary during two weeks. In the first week twice daily (morning and evening), in the second week once daily (evening).

Primary outcomes

  1. Ability and willingness of patients to complete follow-up assessments

    Time frame: after 2 weeks

    the percentage of patients who completed all questionnaires during follow-up

Secondary outcomes

  1. Recruitment of patients; the number of patients that consented and those that declined participation, as well as number of eligible patients.

    Time frame: after 2 weeks

    % of patients

  2. Adherence to advice by patients provided based on the MuSt-PC CDSS

    Time frame: after 2 weeks

    % of patients

  3. Patient impressions of the MuSt-PC CDSS

    Time frame: after 2 weeks

    10 questions with a 4-point Likert scale

  4. Time until symptom burden decreases after the use of the MuSt-PC CDSS based on the filled out Utrecht Symptom Diaries (days)

    Time frame: after 2 weeks

    in days

  5. Feedback about the follow-up assessments within this pilot

    Time frame: after 2 weeks

    open questions

Sponsors and collaborators

Lead sponsor

University Medical Center Groningen

Other

Collaborators

  • Leiden University Medical Center

Registry information

Official study title

The MuSt-PC: A Multidimensional Strategy to Improve Quality of Life of Patients With Multiple Symptoms and Palliative Care Needs - Pilot Study to Assess the Efficacy of a Clinical Decision Support System

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Oct 30, 2023
Registry last updated
Nov 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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