- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07427550
Palliative Care and The Terminally Ill Adults (End of Life) Bill
The Potential Impact of the Terminally Ill Adults (End of Life) Bill on the Professional Identity of Palliative Care Staff
The current study aims to investigate the potential impact of the proposed Assisted Dying (Terminally Ill Adults (2024) Bill on Palliative care workers. Palliative care professionals across the Humber Health Partnership will be interviewed using semi-structured interview questions, with the intention of exploring the way they make sense of the potential implementation of the bill, particularly in relation to their professional identity. The research will be carried out in line with guidance for Interpretative Phenomenological Analysis (Smith, Flowers & Larkin, 2021), a research methodology which aims to explore how people make sense of their experience, often in response to a particular event.
It is hoped that the study will contribute to the ongoing discussions regarding how the bill should be implemented and offer potential insights into ways that hospitals may best support staff during the passing of the bill into law. The study will be sponsored by Hull University Teaching Hospitals Trust (HUTH).
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Dr Matthew Morning, PDCounsPsy
- Phone Number: 01482461060
- Email: matthew.morning1@nhs.net
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Palliative care staff, including Palliative nurses, Doctors and Consultants.
- Registered with the appropriate professional registration body
- Must have been in qualified position and working in palliative care for at least 6 months
- Must have worked with palliative patients in the last three months
- Fluency in English
Exclusion Criteria:
- No direct contact with patients
- Must be in a directly caring role within the team (does not include administrative or housekeeping staff).
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Palliative Care Professionals
Palliative Care Professionals working in a hospital trust in the north of England
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Experiential themes
Time Frame: Taken at the point of interview, two weeks after recruitment.
|
Thematic representations of participant's experiential accounts.
|
Taken at the point of interview, two weeks after recruitment.
|
Collaborators and Investigators
Investigators
- Principal Investigator: Dr Matthew Morning, PDCounsPsych, Hull University Teaching Hospitals Trust
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 354875
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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