PostPartum2ndP: Postpartum Experience by the Second Parent

Sponsor

Université de Reims Champagne-Ardenne (Other)

Overall Status

Not yet recruiting

CT.gov ID

NCT06152159

Collaborator

(none)

100

Enrollment

Locations

Anticipated Duration (Months)

Patients Per Site

Patients Per Site Per Month

Study Details

Study Description

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.

Condition or Disease	Intervention/Treatment	Phase
Postpartum Experience	Other: data collection

Detailed Description

The main objective is to describe the postpartum experience of the second parent.

Study Design

Study Type:

Observational

Anticipated Enrollment :

100 participants

Observational Model:

Case-Only

Time Perspective:

Cross-Sectional

Official Title:

Postpartum Experience by the Second Parent

Anticipated Study Start Date :

Dec 1, 2023

Anticipated Primary Completion Date :

Feb 1, 2024

Anticipated Study Completion Date :

May 1, 2024

Arms and Interventions

Arm	Intervention/Treatment
The second parent of a child The second parent of a child born since minimum 3 months and maximum 6 months.	Other: data collection Data collection

Arm

Intervention/Treatment

The second parent of a child

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

Other: data collection

Data collection

Outcome Measures

Primary Outcome Measures

Experience of the postpartum by the second parent [Day 0]
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

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

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

Exclusion Criteria:

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

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Ufr Medecine Urca	Reims		France	51100
2	Université de Reims Champagne Ardenne	Reims		France	51100

Sponsors and Collaborators

Université de Reims Champagne-Ardenne

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Université de Reims Champagne-Ardenne

ClinicalTrials.gov Identifier:

NCT06152159

Other Study ID Numbers:

2023_RIPH_018_PostPartum-2ndP

First Posted:

Nov 30, 2023

Last Update Posted:

Nov 30, 2023

Last Verified:

Nov 1, 2023

Individual Participant Data (IPD) Sharing Statement:

Undecided

Plan to Share IPD:

Undecided

Studies a U.S. FDA-regulated Drug Product:

Studies a U.S. FDA-regulated Device Product:

Keywords provided by Université de Reims Champagne-Ardenne

postpartum experience

second parent

Study Results

No Results Posted as of Nov 30, 2023