IFPDays: An Intervention to Promote Health Students' Well-being

Sponsor
Groupe Hospitalier du Havre (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05492162
Collaborator
(none)
150
1
16

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: well-being promotion intervention
N/A

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 Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
before/after study using a quasi-experimental designbefore/after study using a quasi-experimental design
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
An Intervention to Promote Health Students' Well-being : a Protocol of a Quasi-experimental Interventional Study in Le Havre
Anticipated Study Start Date :
Sep 1, 2022
Anticipated Primary Completion Date :
Jul 31, 2023
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Other: paramedic students

para-experimental arm

Other: well-being promotion intervention
The intervention will be organized on both conferences and workshops. Four themes will be covered : Well-being (Workshops) Smoking prevention (Conference) Balanced diet (Workshop) Optimal organization for daily healthy living (Conference)

Outcome Measures

Primary Outcome Measures

  1. Well-being [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

Secondary Outcome Measures

  1. Resilience [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

  2. Self-esteem [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

  3. Students' Satisfaction [Month 1]

    Satisfaction data will be analyzed to identify the strengths and the areas for improving the intervention (qualitative and qualitative analyses)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • age >18 years

  • paramedic students enrolled at IFP Mary Thieullent in september 2022

Exclusion Criteria:
  • age < 18 years

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Groupe Hospitalier du Havre

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Groupe Hospitalier du Havre
ClinicalTrials.gov Identifier:
NCT05492162
Other Study ID Numbers:
  • IFPDays
First Posted:
Aug 8, 2022
Last Update Posted:
Aug 8, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Groupe Hospitalier du Havre

Study Results

No Results Posted as of Aug 8, 2022