- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06410560
Culture is Care: Training Workshop for Care Workers (VerbaCurant) (VerbaCurant)
"Culture is Care: Training Workshop for Care Workers" Study
Study Overview
Status
Conditions
Detailed Description
The aim of this project is to identify how a medical humanities intervention can act on the empathic capacity of carers through culture. One of the aims is to introduce an additional element to overcome the problems about language, prejudices, legitimisation by stakeholders who do not yet recognise the value and importance of projects promoting the relationship between culture, wellbeing and health. "Verba Curant" is aimed at generating cultural value, with the hope that it can unite the different professional fields involved and become the heritage of the community.
The project of the Alessandria Hospital Centre in collaboration with the Holden School intends to launch a series of actions aimed at promoting the beneficial impact of culture, in particular storytelling, on the caregivers and patients of the Alessandria Hospital in order to measure how much cultural enjoyment can impact on health literacy. It is planned to define a methodological tool useful for making care workers aware of the importance of culture and dialogue with patients, as well as being able to measure their degree of literacy. The tool will be the object of a widespread training action on care workers, which will also involve all the stakeholders involved in the transmission of health information to patients.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Piedmont
-
Alessandria, Piedmont, Italy, 15121
- Azienda Ospedaliera SS Antonio e Biagio e Cesare Arrigo
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Health professionals related to the Alessandria Hospital
Exclusion Criteria:
- none
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Training workshop with hands-on laboratory
Participants will undergo a training course for a total of 12 hours: 4 FAD + 8 in the laboratory.
They will receive theoretical narrative medicine education with 4 hours of distance education and a practice course of storytelling and creative writing whit 8 hours of distance education in small groups, enabling discussion and interaction among participants.
|
Participants in training courses on creative writing and storytelling.
|
Placebo Comparator: Brief training course
Participants will undergo a training course for a total of 4 FAD hours.
They will receive theoretical narrative medicine education with 4 hours of distance education.
|
Participants in training courses on only theoretical narrative medicine.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Empatic capacity
Time Frame: Before the intervention (Baseline/T0) and immediately after the intervention (Final/T1)
|
Assessment of the empathic capacity of health workers through the Jefferson of Empathy scale in two groups (treated and controls).
|
Before the intervention (Baseline/T0) and immediately after the intervention (Final/T1)
|
Wellbeing
Time Frame: Before the intervention (Baseline/T0) and immediately after the intervention (Final/T1)
|
Assessment of the wellbeing level of health workers through the PGWBI questionnaire in two groups (treated and controls).
|
Before the intervention (Baseline/T0) and immediately after the intervention (Final/T1)
|
Collaborators and Investigators
Investigators
- Principal Investigator: Marinella Bertolotti, Biologist, Azienda Ospedaliera SS Antonio e Biagio e Cesare Arrigo
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- ASO.IRFI.21.02
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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