- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05492162
An Intervention to Promote Health Students' Well-being (IFPDays)
An Intervention to Promote Health Students' Well-being : a Protocol of a Quasi-experimental Interventional Study in Le Havre
The lack of well-being observed among health students underscores the urgent need of implementing interventions designed to meet their specific need and improving their quality of life.
This study aims to evaluate a well-being promotion intervention among paramedic students.
This is a before/after study using a quasi-experimental design. This study aims to compare well-being, resilience, and self-esteem before and after the intervention.
Students' satisfaction will be assessed through a questionnaire.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Health students' well-being is a big issue today. We need to increase the number of interventions designed to improve quality of life and well-being among this population of students.
The investigators aim to evaluate a well-being promotion intervention among paramedic students through a before/after study using a quasi-experimental design by comparing the scores of validated scales of well-being, resilience, and self-esteem of participating students before and after the intervention.
A satisfaction questionnaire will allow to assess the content and the organization of this intervention.
The first edition will be implemented in September 2022 in Le Havre. The questionnaires will be distributed before and eight months after the intervention.
The investigators will describe the study population, then they will compare the average scores.
The results of satisfaction questionnaire will allow to improve the intervention to best meet the needs of students.
The main benefit expected from this study is the improvement of paramedic students' well-being by adopting a healthy lifestyle.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Le Havre, France, 76083
- Groupe Hospitalier Du Havre
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- age >18 years
- paramedic students enrolled at IFP Mary Thieullent in september 2022
Exclusion Criteria:
- age < 18 years
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: paramedic students
para-experimental arm
|
The intervention will be organized on both conferences and workshops. Four themes will be covered :
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Well-being
Time Frame: Month 1 and Month 8
|
Change of average scores of Warwick-Edinburgh Mental Wellbeing Scale - 14 items Scores from 14 to 70: the higher score indicates a better wellbeing
|
Month 1 and Month 8
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Resilience
Time Frame: Month 1 and Month 8
|
Change of average scores of Connor-Davidson Resilience scale - 10 items Scores from 0 to 40: the higher score indicates a strong resilience
|
Month 1 and Month 8
|
|
Self-esteem
Time Frame: Month 1 and Month 8
|
Change of average scores of Rosenberg scale - 10 items Scores from 10 to 40 : the higher score indicates a better self-esteem
|
Month 1 and Month 8
|
|
Students' Satisfaction
Time Frame: Month 1
|
Satisfaction data will be analyzed to identify the strengths and the areas for improving the intervention (qualitative and qualitative analyses)
|
Month 1
|
Collaborators and Investigators
Sponsor
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
- IFPDays
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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