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The MuSt-PC: a Feasibility Study on Intent to Use a Tool With Regard to Symptom Management

Recruiting
Conditions
Palliative Medicine
Interventions
Other: Survey
Registration Number
NCT06110624
Lead Sponsor
University Medical Center Groningen
Brief Summary

A study on the intent to use a tool (MuSt-PC) to manage symptoms of patients in a palliative care trajectory.

Detailed Description

A survey study will be conducted to evaluate if GHCPs have the Intention to Use (IU) MuSt- PC in daily practice. GHCPs are recruited via the connections of the seven Centers of Expertise in Palliative Care. To invite them to participate in the study, the GHCPs are approached directly via e-mail or telephone. Participating GHCPs will be educated on how to use MuSt-PC (educational materials and instruction webinar). GHCPs will be asked to use the CDSS for five individual patients. Every time after using MuSt-PC they will be asked to answer additional questions about their experience with using MuSt-PC in that specific instance. After using MuSt-PC for five patients, they are requested to fill out a comprehensive questionnaire about their overall experiences with using the CDSS.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
20
Inclusion Criteria

Residents (in Dutch: Arts In Opleiding tot Specialist (AIOS) or Arts Niet In Opleiding tot Specialist (ANIOS)), medical specialists and nurse practitioners working in the following disciplines are invited to participate:

  • General practice

  • Nursing home

  • Hospital:

    • Clinical geriatrics
    • Medical oncology
    • Radiation oncology
    • Pulmonology
    • Cardiology
Exclusion Criteria

HCPs who were formally trained in palliative care ("kaderopleiding palliatieve zorg", "Masteropleiding Palliative Medicine for Health Care Professionals at Cardiff University" or "post-HBO opleiding palliatieve zorg") and/or who have been or are currently a consultant of a palliative care consultation team are considered specialists in palliative care, are excluded from participation.

GHCPs (e.g. nurses) who cannot independently decide about CDSS recommendation adherence, including drug interventions, are excluded from participation.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Arm 1SurveyA targeted sample of healthcare providers (HCPs) who are not specialized in palliative care (GHCPs) constitutes the study population.
Primary Outcome Measures
NameTimeMethod
Questions evaluating Intention to Use (IU)after 5 times use of the MuSt-PC tool within 3 months

Questions evaluating Intention to Use (IU) (7-point Likert scales)

Secondary Outcome Measures
NameTimeMethod
Suggestions to improve the MuSt-PC CDSSafter 5 times of the MuSt-PC tool within 3 months

Suggestions to improve the MuSt-PC CDSS (open-ended question).

Questions evaluating other modified TAM domainsafter 5 times use of the MuSt-PC tool within 3 months

Questions evaluating other modified TAM domains: Perceived Usefulness, Perceived Ease-of-Use, Attitude, Compatibility, Subjective norm, Facilitators, Habit (7-point Likert Scales).

Perceived benefits and disadvantages of using MuSt-PCafter 5 times use within 3 months

Perceived benefits and disadvantages of using MuSt-PC (open-ended questions).

Most useful elements of MuSt-PC will be evaluated with a multiple-choice question.after 5 times use within 3 months

Most useful elements of MuSt-PC will be evaluated with a multiple-choice question. (multiple answers allowed) Frequency and percentage of total respondents who chose the multiple choice answer possibilities will be evaluated

Mean scores of HCPs adherence to CDSS recommendationsafter 5 times use of the MuSt-PC tool within 3 months

Mean scores (5-point Likert scale) of HCPs adherence to CDSS recommendations (each time using MuSt-PC)

An overview of the content of questions of participating GHCPs regarding MuSt-PC use.after 5 times use within 3 months

An overview of the content of questions of participating GHCPs regarding MuSt-PC use. Questions will be analyzed qualitatively; coding will be done independently by two researchers. In case of disagreement, consensus will be achieved through discussion. Coding will result in categorization of question subject. Categorizations are ranked from most prevalent to least prevalent question subject (proportion of respondents).

Trial Locations

Locations (2)

University Medical Center Groningen

🇳🇱

Groningen, Netherlands

LUMC

🇳🇱

Leiden, Netherlands

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