Exploring the Role of Nurses in Mobile Palliative Care Teams
Specific Role of Nurse in a Mobile Palliative Care Team (EMSP): Real Autonomy or Utopia
This study looks at how nurses in mobile palliative care teams can better support patients by understanding their needs and improving their care practices.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 25 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospital, Strasbourg, France Academic / other |
| Locations | 1 site (Strasbourg) |
| Trial ID | NCT06113120 on ClinicalTrials.gov |
What this trial studies
This observational study investigates the role and autonomy of State Registered Nurses (IDE) within Mobile Palliative Care Teams (EMSP). It aims to collect and analyze the needs expressed by patients during evaluations initiated by nurses. By examining the professional practices of nurses in various palliative care settings, the study seeks to identify areas for improvement in patient care. The findings could provide insights into how nurses can better support patients in palliative care.
Who should consider this trial
Good fit: Ideal candidates for this study are State-certified nurses working in Mobile Palliative Care Teams within hospital settings.
Not a fit: Patients who are not involved in the care process or who do not consent to the reuse of their data will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the quality of care provided to patients in palliative settings by optimizing the role of nurses.
How similar studies have performed: While there is limited data on this specific focus, similar studies exploring nurse roles in palliative care have shown potential for improving patient outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion criteria: * State-certified nurse working in EMSP with intra- and extra-hospital activity in a CHRU or CHU. * Subject having given their consent for the reuse of their data for the purposes of this research Exclusion criteria: * Subject having expressed opposition to participating in the study
Where this trial is running
Strasbourg
- Service de soins Palliatifs - CHU de Strasbourg - France — Strasbourg, France (Recruiting)
Study contacts
- Study coordinator: Laurent CALVEL, MD, PhD
- Email: laurent.calvel@chru-strasbourg.fr
- Phone: 33 3 88 12 83 39
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.