NCT06152159

Brief Summary

Many studies have been performed on mothers and their postnatal experiences. Unfortunately, studies about the second parent are very rare. Second parent is yet an essential figure in the parent-child triad and a real support for the mother. The postpartum period is a time of intense restructuring and upheaval, both physically and psychologically. Studies have shown that almost 13% of fathers suffer from depression.

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
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Dec 2023

Shorter than P25 for all trials

Geographic Reach
1 country

2 active sites

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

November 21, 2023

Completed
9 days until next milestone

First Posted

Study publicly available on registry

November 30, 2023

Completed
1 day until next milestone

Study Start

First participant enrolled

December 1, 2023

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2024

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2024

Completed
Last Updated

November 30, 2023

Status Verified

November 1, 2023

Enrollment Period

2 months

First QC Date

November 21, 2023

Last Update Submit

November 21, 2023

Conditions

Postpartum Experience

Keywords

postpartum experiencesecond parent

Outcome Measures

Primary Outcomes (1)

  • Experience of the postpartum by the second parent

    This experience of the postpartum by the second parent will be evaluated by a Likert scale with 5 proposals: Very good experience/ Good experience/ Lived/neutral/ Bad experience/ Very bad experience

    Day 0

Study Arms (1)

The second parent of a child

The second parent of a child born since minimum 3 months and maximum 6 months.

Other: data collection

Interventions

data collectionOTHER

Data collection

The second parent of a child

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The second parent of a child born since minimum 3 months and maximum 6 months.

You may qualify if:

  • Males and females
  • Second parent of a child born living for at least 3 months and at most 6 months
  • Major
  • Agreeing to participate in the study

You may not qualify if:

  • Minors
  • Protected by law (guardianship, curatorship, safeguarding of justice)
  • Not agreeing to participate in this study
  • Parents of stillborn children
  • Refusing to participate in the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Ufr Medecine Urca

Reims, 51100, France

Location

Université de Reims Champagne Ardenne

Reims, 51100, France

Location

MeSH Terms

Interventions

Data Collection

Intervention Hierarchy (Ancestors)

Epidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Central Study Contacts

Barbe Coralie, DR

CONTACT

0326913665coralie.barbe@univ-reims.fr

Parisot Céline

CONTACT

06.24.98.62.80celine.parisot@ch-epernay.fr

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 21, 2023

First Posted

November 30, 2023

Study Start

December 1, 2023

Primary Completion

February 1, 2024

Study Completion

May 1, 2024

Last Updated

November 30, 2023

Record last verified: 2023-11

Locations

FR(2)