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French Cross-cultural Adaptation of the Iowa Infant Feeding Attitude Scale (IIFAS) (FRENCH IIFAS)

27 maggio 2026 aggiornato da: BARASINSKI Chloé, University Hospital, Clermont-Ferrand

French Cross-cultural Adaptation of the Iowa Infant Feeding Attitude Scale (IIFAS) and Assessments of Parental Representations of Infant Feeding During Pregnancy in the Auvergne Perinatal Network.

Our study will consist of two parts:

  • Part 1: Cross-cultural adaptation of the Iowa Infant Feeding Attitude Scale (IIFAS) among postpartum mothers and co-parents in France and assessment of its psychometric properties
  • Part 2: Assessment of cultural representations of infant feeding practices during pregnancy.

The goal of this repeated cross-sectional study is to cross-culturally adapt and evaluate the psychometric properties of the French version of the IIFAS among postpartum mothers in France.

In the part 1 of the study, the main questions it aims to answer are:

  • Evaluation of the psychometric properties of the French version of the Iowa Infant Feeding Attitude Scale (IIFAS) among postpartum mothers in France
  • Evaluation of the psychometric properties of the French version of the Iowa Infant Feeding Attitude Scale (IIFAS) among postpartum co-parents in France

Participants will be asked :

  • to complete the study questionnaires, including the French version of the IIFAS questionnaire.
  • to complete the French version of the IIFAS questionnaire a second time 7 days after their initial completion.
  • to answer 1 to 4 questions about the infant's current feeding regimen 8 weeks after giving birth.

In the part 2, the goal of this descriptive cross-sectional study is to assess cultural representations of infant feeding practices during pregnancy among pregnant women in France during the first and the third trimesters.

In the part 2 of the study, the main questions it aims to answer are:

  • To describe cultural perceptions of infant feeding practices among mothers in France during the first and third trimesters of pregnancy.
  • To describe the cultural perceptions of infant feeding practices among co-parents in France during the first and third trimesters of pregnancy.
  • To compare the cultural perceptions of infant feeding practices among mothers according to the trimester of pregnancy.
  • To analyze the impact of different factors (age, education level, occupation, number of children, geographic origin, socioeconomic status, having been breastfed oneself, having personal experience with breastfeeding, plans to return to work, etc.) on mothers' cultural perceptions of infant feeding practices during the first and third trimesters of pregnancy.
  • To compare co-parents' cultural perceptions of infant feeding methods according to the trimester of pregnancy.
  • To analyze the impact of different factors (age, education level, occupation, number of children, geographic origin, socioeconomic status, having been breastfed oneself, having a child who was previously breastfed, etc.) on co-parents' cultural perceptions of infant feeding methods during the first and third trimesters of pregnancy.
  • To compare the cultural perceptions of infant feeding practices between mothers and co-parents during the first and third trimesters of pregnancy.

Participants will be asked to complete the study questionnaires, including the French version of the IIFAS questionnaire.

Panoramica dello studio

Stato

Non ancora reclutamento

Tipo di studio

Osservativo

Iscrizione (Stimato)

930

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • France
      • Clermont-Ferrand, France, Francia, 63000
        • CHU de Clermont-Ferrand
        • Investigatore principale:
          • Chloé BARASIONSKI

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

N/A

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

For part 1, Our target population will consist of new parents during their stay in the maternity ward at one of the Auvergne Perinatal Network maternity participating in the study.

For part 2, our target population will be expectant parents during pregnancy who are receiving care within the Auvergne Perinatal Network. Participation by both parents is not required for this study.

Descrizione

Part 1

Inclusion Criteria:

  • Adult women hospitalized for postpartum care in one of the 10 maternity hospitals of the Auvergne perinatal network participating in the project, and/or adult co-parents whose partner is hospitalized in one of the 10 RSPA maternity hospitals participating in the project,
  • Mothers and/or co-parents of a singleton child born alive at term (≥37 weeks' gestation) and hospitalized in the maternity ward,
  • Mothers and/or co-parents of a child less than 6 days old,
  • Mothers and/or co-parents affiliated to a social security scheme,
  • Mothers and/or co-parents capable of reading and understanding French.

Non-inclusion Criteria:

  • Mothers and/or co-parents of a child hospitalized outside the maternity ward,
  • Mothers and/or co-parents who are adults with legal incapacity (under guardianship, conservatorship, or judicial protection),
  • Mothers and/or co-parents who refuse to participate in the study,
  • Mothers with a contraindication to AM and/or co-parents whose spouse has a contraindication to AM,
  • Mothers and/or co-parents of a child with a medical condition or malformation that affects their feeding.

Part 2 during 1st trimester :

Inclusion Criteria:

  • Pregnant adult women who are being cared for by healthcare professional belonging the Auvergne perinatal network and/or their co-parents of legal age, during the first trimester of pregnancy (before 16 weeks and 0 days of gestation),
  • Pregnant women and/or co-parents affiliated to a social security scheme,
  • Pregnant women and/or co-parents who can read and understand French.

Non-inclusion criteria :

  • Pregnant women and/or co-parents in the second trimester of pregnancy (between 16 weeks 0 days and 28 weeks 6 days of gestation),
  • Pregnant women and/or co-parents who are legally incapacitated adults (under guardianship, conservatorship, or judicial protection),
  • Pregnant women and/or co-parents who refuse to participate in the study,
  • Pregnant women with a contraindication to breastfeeding and/or co-parents whose partner has a contraindication to breastfeeding,
  • Pregnant women with a multiple pregnancy and/or co-parents being monitored for a multiple pregnancy.

Part 2 during 3rd trimester :

Inclusion Criteria:

  • Pregnant adult women who are being cared for by healthcare professional belonging the Auvergne perinatal network and/or their co-parents of legal age, during the third trimester of pregnancy (after 28 weeks and 6 days of gestation),
  • Pregnant women and/or co-parents affiliated to a social security scheme,
  • Pregnant women and/or co-parents who can read and understand French.

Non-inclusion criteria :

  • Pregnant women and/or co-parents in the second trimester of pregnancy (between 16 weeks 0 days and 28 weeks 6 days of gestation),
  • Pregnant women and/or co-parents who are legally incapacitated adults (under guardianship, conservatorship, or judicial protection),
  • Pregnant women and/or co-parents who refuse to participate in the study,
  • Pregnant women with a contraindication to breastfeeding and/or co-parents whose partner has a contraindication to breastfeeding,
  • Women and/or co-parents of a child with a medical condition or malformation affecting the child's feeding,
  • Pregnant women with a multiple pregnancy and/or co-parents being monitored for a multiple pregnancy.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

Coorti e interventi

Gruppo / Coorte
Part 1 : Cross-cultural adaptation
196 mothers and 196 co-parents
Part 2 : Cultural representations during 1st trimester
155 pregnant women and 155 co-parents in the first : 310 people in all
Part 2 : Cultural representations during 3rd trimester
155 pregnant women and 155 co-parents in the third trimester of pregnancy: 310 people in all

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
French-IIFAS for mothers [Part 1]
Lasso di tempo: 0 day
Psychometric properties (acceptability, floor effect, internal validity, internal consistency, construct validity) of the French version of the Iowa Infant Feeding Attitude Scale (IIFAS) among postpartum mothers in France
0 day
French-IIFAS scores for pregnant women [Part 2 1st trimester] [Part 2 3rd trimester]
Lasso di tempo: 0 day
The item scores and total scores obtained by pregnant women at the first and third trimesters of pregnancy
0 day

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change of French-IIFAS from baseline at 7 days for mothers [Part 1]
Lasso di tempo: 7 days
Test-retest reliability of the French version of the IIFAS questionnaire among mothers
7 days
Predictive value of French-IIFAS among mothers [Part 1]
Lasso di tempo: 0 day, 8 weeks
Predictive value of the score French-IIFAS questionnaire with the infant's feeding method at 8 weeks postpartum among mothers
0 day, 8 weeks
French-IIFAS for co-parents [Part 1]
Lasso di tempo: 0 day
Psychometric properties Psychometric properties (acceptability, floor effect, internal validity, internal consistency, construct validity) of the French version of the Iowa Infant Feeding Attitude Scale (IIFAS) among postpartum coparents in France
0 day
Change of French-IIFAS from baseline at 7 days for coparents [Part 1]
Lasso di tempo: 0 day, 7 days
Test-retest reliability of the French version of the IIFAS questionnaire among coparents
0 day, 7 days
Predictive value of French-IIFAS among coparents [Part 1]
Lasso di tempo: 0 day, 8 weeks
Predictive value of the score French-IIFAS questionnaire with the infant's feeding method at 8 weeks postpartum among coparents
0 day, 8 weeks
French-IIFAS scores for co-parents [Part 2 1st trimester] [Part 2 3rd trimester]
Lasso di tempo: 0 day
The item scores and total scores obtained by co-parents at the first and third trimesters of pregnancy
0 day
Differences in French-IIFAS scores for pregnant women between the first and third trimesters of pregnancy [Part 2 1st trimester] [Part 2 3rd trimester]
Lasso di tempo: 0 day
The item scores and total French-IIFAS questionnaire scores obtained by pregnant women will be compared between the first and third trimesters
0 day
Differences in French-IIFAS scores for co-parents between the first and third trimesters of pregnancy [Part 2 1st trimester] [Part 2 3rd trimester]
Lasso di tempo: 0 day
The item scores and total French-IIFAS questionnaire scores obtained by the co-parents will be compared between the first and third trimesters
0 day
Background, socio-demographic and medical characteristics of pregnant women [Part 2 1st trimester] [Part 2 3rd trimester]
Lasso di tempo: 0 day
Age, educational level, occupation, number of children, marital status, geographic origin, socioeconomic status, having been breastfed oneself, having personal experience with breastfeeding, having a child who has already been breastfed, optimal duration of breastfeeding, influence of the infant's feeding method on the couple's lifestyle, parent-child relationship, women's body image, plans to return to work after childbirth, intended feeding method.
0 day
Background, socio-demographic and medical characteristics of co-parents [Part 2 1st trimester] [Part 2 3rd trimester]
Lasso di tempo: 0 day
Age, educational level, occupation, number of children, marital status, geographic origin, socioeconomic status, having been breastfed oneself, having personal experience with breastfeeding, having a child who has already been breastfed, optimal duration of breastfeeding, influence of the infant's feeding method on the couple's lifestyle, parent-child relationship, women's body image, plans to return to work after childbirth, intended feeding method.
0 day
Differences in scores between mothers and co-parents [Part 2 1st trimester] [Part 2 3rd trimester]
Lasso di tempo: 0 day
Item scores and the total score on the IIFAS questionnaire will be compared between mothers and co-parents during the first and third trimesters of pregnancy
0 day

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Chloé BARASINSKI, University Hospital, Clermont-Ferrand

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

27 maggio 2026

Completamento primario (Stimato)

27 gennaio 2028

Completamento dello studio (Stimato)

27 gennaio 2029

Date di iscrizione allo studio

Primo inviato

27 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

27 maggio 2026

Primo Inserito (Effettivo)

2 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

2 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

27 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • RNI 2025 BARASINSKI
  • ANSM (Altro identificatore: 2025-A02921-48)

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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