Ta strona została przetłumaczona automatycznie i dokładność tłumaczenia nie jest gwarantowana. Proszę odnieść się do angielska wersja za tekst źródłowy.

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

27 maja 2026 zaktualizowane przez: 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.

Przegląd badań

Status

Jeszcze nie rekrutacja

Typ studiów

Obserwacyjny

Zapisy (Szacowany)

930

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Lokalizacje studiów

    • France
      • Clermont-Ferrand, France, Francja, 63000
        • CHU de Clermont-Ferrand
        • Główny śledczy:
          • Chloé BARASIONSKI

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie dotyczy

Metoda próbkowania

Próbka bez prawdopodobieństwa

Badana populacja

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.

Opis

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.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

Kohorty i interwencje

Grupa / 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 mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
French-IIFAS for mothers [Part 1]
Ramy czasowe: 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]
Ramy czasowe: 0 day
The item scores and total scores obtained by pregnant women at the first and third trimesters of pregnancy
0 day

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Change of French-IIFAS from baseline at 7 days for mothers [Part 1]
Ramy czasowe: 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]
Ramy czasowe: 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]
Ramy czasowe: 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]
Ramy czasowe: 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]
Ramy czasowe: 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]
Ramy czasowe: 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]
Ramy czasowe: 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]
Ramy czasowe: 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]
Ramy czasowe: 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]
Ramy czasowe: 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]
Ramy czasowe: 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

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Śledczy

  • Główny śledczy: Chloé BARASINSKI, University Hospital, Clermont-Ferrand

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

27 maja 2026

Zakończenie podstawowe (Szacowany)

27 stycznia 2028

Ukończenie studiów (Szacowany)

27 stycznia 2029

Daty rejestracji na studia

Pierwszy przesłany

27 maja 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

27 maja 2026

Pierwszy wysłany (Rzeczywisty)

2 czerwca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

2 czerwca 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

27 maja 2026

Ostatnia weryfikacja

1 maja 2026

Więcej informacji

Terminy związane z tym badaniem

Dodatkowe istotne warunki MeSH

Inne numery identyfikacyjne badania

  • RNI 2025 BARASINSKI
  • ANSM (Inny identyfikator: 2025-A02220-49)

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

Subskrybuj