Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID06594263

Cross-cultural Adaptation and Validation of the French Version of the PAPA Questionnaire Assessing Fathers' Psychological Experience Before and After Birth

Led by University Hospital, Clermont-Ferrand · Updated on 2025-08-14

340

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to adapt and validate a French version of the Perinatal Assessment of Paternal Affectivity (PAPA) questionnaire, designed to screen for mental health challenges in fathers during the pre- and postnatal periods. The study addresses the need for a gender-sensitive tool to detect paternal symptoms like anxiety, depression, stress, irritability, and other psychological difficulties, which may differ from those traditionally seen in mothers. Researchers seek to provide a simple, effective way to identify paternal psychological distress in French-speaking populations. The study involves cross-cultural adaptation of the PAPA questionnaire into French, following international guidelines. Male partners of pregnant women or new mothers will complete the questionnaire online either during the third trimester of pregnancy or eight weeks after childbirth. The PAPA assesses eight key areas of mental health symptoms with a 4-point scale, plus additional questions on the fathers' feelings about parenthood. A test-retest reliability check will be performed by having participants complete the questionnaire a second time 10 days after the first. Participants will provide informed consent, and women will not complete questionnaires but their medical and demographic data will be collected. The study will collect data on paternal mental health through questionnaires completed online, along with socio-demographic and medical data from both partners. Researchers will evaluate the reliability of the French-PAPA tool and compare it with other measures like anxiety, depression, and stress scales. The study is observational and participation lasts from the prenatal or postnatal questionnaire completion through the follow-up 10 days later.

CONDITIONS

Brief Title

Validation of the French Version of the Perinatal Assessment of Paternal Affectivity (PAPA)

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Woman and her male partner aged 18 years or older
  • Both partners understand, speak, and read French
  • Both partners voluntarily agree to participate and provide informed consent
Not Eligible

You will not qualify if you...

  • Woman without a male partner
  • Woman admitted to intensive care after giving birth
  • Couple whose newborn died around the time of birth
  • Couple with a medical abortion or fetal death in current pregnancy
  • Woman or male partner refusing to participate
  • Woman or male partner not speaking French
  • Woman or male partner unable to answer questionnaires
  • Woman or male partner under legal guardianship, deprived of liberty, or in custody

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Baseline on one day

Male partners complete the French-PAPA questionnaire and other related assessments online to evaluate psychological experience before or after birth.

1 online questionnaire completion

Diagnostic Evaluation

Duration - 10 days after baseline

Male partners complete the French-PAPA questionnaire a second time online 10 days after the first completion to assess test-retest reliability.

1 online questionnaire completion

Trial Site Locations

Total: 1 location

1

CHU Clermont-Ferrand

Clermont-Ferrand, France

Actively Recruiting

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Research Team

L

Lise Laclautre

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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