- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02681874
Smart and Secure Children Program for Preschool Obesity (SSC)
Feasibility Study of the Modified-Smart and Secure Children Program in Primary Care
Many behavioral interventions designed to improve dietary patterns for ethnic and racial/minority preschoolers have produced modest outcomes. A limitation of these interventions include a failure to address key factors associated with dietary patterns for these children, such as parental stress levels. Therefore, the identification of intervention models that target these factors and are effective, acceptable, and feasible among parents of young minority children is important.
Subjects will be asked to take part in this study because they are the parents of a child that receives care at a Texas Children's Pediatrics (TCP) clinic where the study is being done and their child's body mass index has been at or above the 85th percentile.
The purpose of this pilot study is to assess the ease and acceptance of providing an intervention for parents of children ages 2-5 years in the pediatric primary care clinic. The purpose is to also assess how well the intervention works in improving the child's dietary patterns.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Thirty (30) subjects will be enrolled across three (3) TCP clinics where the study will take place. Two types of participants will be recruited for this study: parent participants who will receive the intervention and interventionist participants who will deliver the intervention.
Data collected for this study includes 4 types: parent-report questionnaires, parent saliva samples, parent-report of children's 24-hour food recall, and audio-recordings of intervention sessions. Parent-report questionnaires will assess family demographic information, parental stress, depression, and well-being as well as parental feeding practices and child dietary food patterns.
Procedures for Parent Participants:
Parents will be randomized to the intervention (Group A-15 parents) or control condition (Group B-15 parents). Parents who are randomized to the intervention group will then participate in the 10-session SSC program that is co-led by a trained parent interventionist. Sessions will be audio-recorded to allow intervention fidelity checks. Parents who are randomized to the control condition will receive the SSC written handouts, which is enhanced standard of care for parents who are seen in primary care.
If subjects are assigned to Group A, they will participate in ten intervention sessions that are conducted in the TCP clinic. During each session, subjects will be provided with information about specific skills to improve their child's emotional health and dietary patterns and their own stress levels.
If subjects are assigned to Group B, they will receive written handouts about children's dietary patterns and parent stress levels. They will be instructed to write goals and document goal progress. This care plan is the standard practice and is presently implemented in the site's TCP clinics.
After ten weeks, regardless of the group the subjects were assigned to, they will again complete an interview about their child's dietary food patterns and questionnaires about their own emotions/opinions of their parenting and child feeding practices. The subjects will also be asked to collect their saliva at four time points on a single day at home.
Procedures for Interventionist Participants:
Six interventionist participants will be recruited. Those who indicate interest will meet with the PI or a research staff member to obtain consent. They will then receive 40-hours of training in the intervention provided by study staff. Intervention participants will deliver one or more group intervention, which has 10 sessions.
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Texas
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Houston, Texas, Estados Unidos, 77030
- Texas Children's Hospital
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Houston, Texas, Estados Unidos, 77030
- Texas Children's Pediatric Associates (TCPA)
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria for Parent Participants:
- Non-Latino African American or Latino parents/primary caregivers (defined as primary guardian, which may include legal guardians and foster parents) of a child patient (ages 2-5 years) at Texas Children's Pediatrics (TCP) Community Care medical practices (Gulfgate, Cullen, and Corinthian Pointe)
- Parents of children with a body mass index (BMI) of greater than 85th and less than 95th percentile (overweight) and greater than 95th percentile (obese)
- English as the primary household language
Inclusion Criteria for Interventionist Participants:
- Non-Latino African American or Latino, 18 years or older, having a GED/high school diploma, and parent of a young child
Exclusion Criteria for Parent Participants:
- Parents of children with any type of food allergy, parents of children receiving current intervention for weight
- Parents of children with weight-related medical conditions (e.g., Prader-Willi Syndrome)
- Parents of children who are taking medication (e.g.,stimulant) associated with appetite
Exclusion Criteria for Parent Participants:
- None
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
---|---|
Experimental: Group A (Treatment Arm)
The Smart and Secure Children (SSC) program is a 10-week manualized intervention that uses a written validated curriculum.
The program is group-based and co-led by peer leaders (Parent Leaders).
Sessions are 90 minutes.
Groups consist of a maximum of five parents.
Parent Leaders facilitate conversations on the SSC program content by sharing real life application, experiences, and solutions.
Parent Leaders receive a week-long leadership training to deliver the program and will be supervised by the PI who is a licensed clinical psychologist.
|
The Smart and Secure Children (SSC) program is a 10-week manualized intervention that uses a written validated curriculum.
The program is group-based and co-led by peer leaders (Parent Leaders).
Parent Leaders facilitate conversations on the SSC program content by sharing real life application, experiences, and solutions.
|
Comparador activo: Group B (Control Arm)
Parents in the control condition will receive the Smart and Secure Children (SSC) program's written handouts.
Handouts include didactic curriculum content and instruct parents to write goals and document goal progress.
|
The handouts are a part of the SSC program that include didactic curriculum content and instruct parents to write goals and document goal progress.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Increase in Healthy Food Dietary Patterns
Periodo de tiempo: 5 months
|
24-hour recalls conducted with parents will be used to assess children's intake of vegetables, fruits, whole grains, and low/non-fat dairy
|
5 months
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Decrease in Parental Stress
Periodo de tiempo: 5 months
|
Parent perceived general stress will be assessed using the Perceived Stress Scale.
|
5 months
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Decrease in Parental Stress
Periodo de tiempo: 5 months
|
Parent perceived parenting stress will be assessed using the Parenting Stress Index-Short Form.
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5 months
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Decrease in Parental Stress
Periodo de tiempo: 5 months
|
Diurnal cortisol rhythm levels will be determined by obtaining samples of parents' saliva.
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5 months
|
Parental Mental Health Improvement
Periodo de tiempo: 5 months
|
The Center for Epidemiological Depression Studies Scale will be used to determine parental depressive symptoms.
|
5 months
|
Parental Mental Health Improvement
Periodo de tiempo: 5 months
|
The Mental Health Continuum-Short Form will be used to measure parents' positive mental health symptoms.
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5 months
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Improvement in Parental Feeding Behaviors
Periodo de tiempo: 5 months
|
Parental feeding behaviors will be assessed using The Child Feeding Questionnaire.
|
5 months
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Ashley Butler, Ph.D, Baylor College of Medicine
Publicaciones y enlaces útiles
Enlaces Útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- H-37460
- 46486-I (Otro número de subvención/financiamiento: Texas Children's Hospital Pediatric Pilot Award)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
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. .
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