"Improved Mother Infant Feeding Interaction (MI-FI) at 12 Months With Very Early Parent Training" (MI-FI)
5 de junio de 2017 actualizado por: Rambam Health Care Campus
"Improved Mother Infant Feeding Interaction (MI-FI) at 12 Months With Very Early Parent
Rise in childhood obesity and poor eating habits and eating problems is apparent over the last decades.
Parents are at lose what the correct way to tackle these problems may be.
This study examined whether professional behavioral and nutritional training of first time mothers improves feeding relationship and infants eating habits at 12 months.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Descripción detallada
From 166 first time mother-infant recruited, 128 completed the trail.
Intervention group, mother-infant dyads got a month long weekly based training in small workshop groups about nutrition, feeding and parenting when infants were 4-6 months old.
training was given by a highly experience pediatric dietitian and social worker.
Thereafter, internet-based support continued until infants reached 12 months.
The control group received customary support via municipal mother-child health clinics.
Mealtime interactions were videotaped at home setting at 12 months and were evaluated using the Chatoor feeding scale by blinded (to group) viewers.
Tipo de estudio
Intervencionista
Inscripción (Actual)
166
Fase
- No aplica
Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
23 años a 35 años (Adulto)
Acepta Voluntarios Saludables
Sí
Géneros elegibles para el estudio
Femenino
Descripción
Inclusion Criteria:
- normal and healthy pregnancy
- full term delivery of infants
- infants with a normal birth weight and no health problems
- Mothers recruited had at least a high school education
- mothers lived near to or in the city (important for video taping)
Exclusion Criteria:
- Mothers with mental illness in the present or the past (such as schizophrenia, depression or an eating disorder)
- infants with chronic diseases that required specific diets (such as milk allergy) or gastrointestinal diseases (celiac disease, type 1 diabetes, Crohn's disease etc.)
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: intervention group
First time mothers, when infants were ages 4-6 months old, took part in a training program in small group setting (10-12 mother-infants).
the program continued for a month, with 4 weekly meetings.
group coordinators were a highly experienced pediatric dietitian, and a social worker.
Training topics addressed were infant healthy nutrition and growth, feeding skills, obesity and emotional feeding prevention, parenting.
Thereafter, mothers were encouraged to stay in contact with the trainers, till infants reached age 12 months and data was collected using video taping of mealtime feeding interactions at home setting environment.
Mother Infant Feeding Interaction very early training
|
weekly training meetings on 4 topics:
|
|
Sin intervención: control group
Control group first time mothers were recruited when infants were around 11-12 months of age for data collection of mealtime feeding interactions taping at home setting environment.
They received during this year the official support and training given in municipality care centers.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Chatoor feeding scale
Periodo de tiempo: 12 months
|
the Chatoor observational scale for Mother-Infant interaction during feeding was purchased from the Chatoor Center.
The Scale consists of 46 mother and infant behavior modes which are rated throughout the feeding session.
Five subscale scores are derived: 1) Dyadic Reciprocity, 2) Dyadic Conflict, 3) Talk and Distraction, 4) Struggle for Control, and 5) Maternal Non-Contingency.
The CFS has been demonstrated to discriminate between infants with and without feeding disorders and can be used with infants and toddlers ranging from 1 month to 3 years of age (Chatoor et al, 1997).
|
12 months
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
eating habitts
Periodo de tiempo: 12 months
|
Self reported questionnaires of Golan et al checking eating habits and obesogenic environment at home
|
12 months
|
Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Investigadores
- Investigador principal: Ron Shaoul, MD, Pediatric Gastroenterology Unit, Ruth Rappaport Children's Hospital Rambam Health Care Campus, Haifa, Israel, Rappaport Faculty of Medicine;
Publicaciones y enlaces útiles
La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.
Publicaciones Generales
- Redsell SA, Edmonds B, Swift JA, Siriwardena AN, Weng S, Nathan D, Glazebrook C. Systematic review of randomised controlled trials of interventions that aim to reduce the risk, either directly or indirectly, of overweight and obesity in infancy and early childhood. Matern Child Nutr. 2016 Jan;12(1):24-38. doi: 10.1111/mcn.12184. Epub 2015 Apr 20.
- Ammaniti M, Lucarelli L, Cimino S, D'Olimpio F, Chatoor I. Feeding disorders of infancy: a longitudinal study to middle childhood. Int J Eat Disord. 2012 Mar;45(2):272-80. doi: 10.1002/eat.20925. Epub 2011 Apr 14.
- Bryant-Waugh R, Markham L, Kreipe RE, Walsh BT. Feeding and eating disorders in childhood. Int J Eat Disord. 2010 Mar;43(2):98-111. doi: 10.1002/eat.20795.
- Meadows N. Assessment and management of feeding difficulties in infants. Community Pract. 2015 Feb;88(2):45-7. No abstract available.
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Actual)
25 de octubre de 2011
Finalización primaria (Actual)
21 de julio de 2013
Finalización del estudio (Actual)
21 de julio de 2013
Fechas de registro del estudio
Enviado por primera vez
16 de marzo de 2017
Primero enviado que cumplió con los criterios de control de calidad
16 de marzo de 2017
Publicado por primera vez (Actual)
22 de marzo de 2017
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
7 de junio de 2017
Última actualización enviada que cumplió con los criterios de control de calidad
5 de junio de 2017
Última verificación
1 de junio de 2017
Más información
Términos relacionados con este estudio
Otros números de identificación del estudio
- 0156-11-RMB
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
INDECISO
Descripción del plan IPD
The investigators plan to publish results of the research project in peer reviewed journals.
However, individual data collected, such as video taping of family meals will not be shared.
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .