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

27. května 2026 aktualizováno: 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.

Přehled studie

Postavení

Zatím nenabíráme

Typ studie

Pozorovací

Zápis (Odhadovaný)

930

Kontakty a umístění

Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.

Studijní kontakt

Studijní místa

    • France
      • Clermont-Ferrand, France, Francie, 63000
        • CHU de Clermont-Ferrand
        • Vrchní vyšetřovatel:
          • Chloé BARASIONSKI

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

  • Dospělý
  • Starší dospělý

Přijímá zdravé dobrovolníky

N/A

Metoda odběru vzorků

Vzorek nepravděpodobnosti

Studijní populace

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.

Popis

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.

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

Kohorty a intervence

Skupina / kohorta
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

Co je měření studie?

Primární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
French-IIFAS for mothers [Part 1]
Časové okno: 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]
Časové okno: 0 day
The item scores and total scores obtained by pregnant women at the first and third trimesters of pregnancy
0 day

Sekundární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Change of French-IIFAS from baseline at 7 days for mothers [Part 1]
Časové okno: 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]
Časové okno: 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]
Časové okno: 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]
Časové okno: 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]
Časové okno: 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]
Časové okno: 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]
Časové okno: 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]
Časové okno: 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]
Časové okno: 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]
Časové okno: 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]
Časové okno: 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

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Vyšetřovatelé

  • Vrchní vyšetřovatel: Chloé BARASINSKI, University Hospital, Clermont-Ferrand

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia (Odhadovaný)

27. května 2026

Primární dokončení (Odhadovaný)

27. ledna 2028

Dokončení studie (Odhadovaný)

27. ledna 2029

Termíny zápisu do studia

První předloženo

27. května 2026

První předloženo, které splnilo kritéria kontroly kvality

27. května 2026

První zveřejněno (Aktuální)

2. června 2026

Aktualizace studijních záznamů

Poslední zveřejněná aktualizace (Aktuální)

2. června 2026

Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality

27. května 2026

Naposledy ověřeno

1. května 2026

Více informací

Termíny související s touto studií

Další relevantní podmínky MeSH

Další identifikační čísla studie

  • RNI 2025 BARASINSKI
  • ANSM (Jiný identifikátor: 2025-A02921-48)

Informace o lécích a zařízeních, studijní dokumenty

Studuje lékový produkt regulovaný americkým FDA

Ne

Studuje produkt zařízení regulovaný americkým úřadem FDA

Ne

Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .

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