NCT04338594

Brief Summary

Professional constraints can have major causes on personal and couple life. In particular, some professions with major professional constraints that can be particularly impacted, such as doctors and healthcare workers. The main objective was to demonstrate the impact of work on the desire and the fact to have children

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
10,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2020

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 4, 2020

Completed
4 days until next milestone

First Posted

Study publicly available on registry

April 8, 2020

Completed
23 days until next milestone

Study Start

First participant enrolled

May 1, 2020

Completed
5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2025

Completed
Last Updated

April 8, 2020

Status Verified

March 1, 2020

Enrollment Period

5 years

First QC Date

April 4, 2020

Last Update Submit

April 4, 2020

Conditions

Parenthood Status

Keywords

ParenthoodWorkchild

Outcome Measures

Primary Outcomes (1)

  • parenthood

    The desire to have a child and the parenting management will be assessed by questionnaires

    Day 1

Secondary Outcomes (2)

  • Sociodemographic characteristics

    Day 1

  • occupation perception

    Day 1

Eligibility Criteria

Age16 Years+
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Workers or retirees

You may qualify if:

  • All volunteers
  • Workers or retirees

You may not qualify if:

  • none

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University hospital, Clermont-Ferrand

Clermont-Ferrand, 63000, France

Location

Central Study Contacts

Lise Laclautre

CONTACT

0473754963promo_interne_drci@chu-clermontferrand.fr

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Target Duration
1 Day
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 4, 2020

First Posted

April 8, 2020

Study Start

May 1, 2020

Primary Completion

May 1, 2025

Study Completion

May 1, 2025

Last Updated

April 8, 2020

Record last verified: 2020-03

Locations

FR(1)