Work-related Stress Among Recently Graduated Midwives Practicing in the Delivery Room (Stress-SF)

December 2, 2022 updated by: Université de Reims Champagne-Ardenne

At work, stress results of an imbalance between the worker's hopes and the reality of working conditions.

Midwives are exposed to emergency situations (newborn distress, neonatal resuscitation, foetal abnormal heart rythm, delivery hemorrhage, …), which can cause stress and sometimes lead to burnout.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

the aim of the study is to describe Work-related stress among recently graduated midwives practicing in the delivery room

Study Type

Observational

Enrollment (Anticipated)

500

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

  • France
      • Reims, France, 51100
        • Recruiting
        • Université de Reims Champagne Ardenne
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Midwives graduated for less than three years practicing in the delivery room

Description

Inclusion Criteria:

  • Midwives graduated for less than three years in France Practicing in the delivery room Whatever the duration of exercise in the delivery room Agreeing to participate in the study

Exclusion Criteria:

  • No Agreeing to participate in the study

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Only
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
group "recently graduated midwives practicing in the delivery room"
Midwives graduated for less than three years and practicing in the delivery room
Other: data collection
Work-related stress evaluation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Work-related stress
Time Frame: Day 0
Work-related stress evaluated using Perceived Stress Scale (PPS10). PPS10 includes 10 items evaluating the degree to which an individual has perceived life as unpredictable, uncontrollable and overloading over the previous month. Each item is coded from 1 to 4 points: never, almost never, sometimes, fairly often and very often. The overall score ranges from 0 to 40 points.
Day 0

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Université de Reims Champagne-Ardenne

Investigators

  • Principal Investigator: Le Tarnec Louise Anne, Dr, Université de Reims Champagne-Ardenne

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2022

Primary Completion (Anticipated)

February 1, 2023

Study Completion (Anticipated)

April 1, 2023

Study Registration Dates

First Submitted

December 2, 2022

First Submitted That Met QC Criteria

December 2, 2022

First Posted (Estimate)

December 13, 2022

Study Record Updates

Last Update Posted (Estimate)

December 13, 2022

Last Update Submitted That Met QC Criteria

December 2, 2022

Last Verified

December 1, 2022

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2022_RIPH_009_Stress-SF

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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