- ICH GCP
- US Clinical Trials Registry
- Clinical Trial 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.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
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.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Texas
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Houston, Texas, United States, 77030
- Texas Children's Hospital
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Houston, Texas, United States, 77030
- Texas Children's Pediatric Associates (TCPA)
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
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.
|
Active Comparator: 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.
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The handouts are a part of the SSC program that include didactic curriculum content and instruct parents to write goals and document goal progress.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Increase in Healthy Food Dietary Patterns
Time Frame: 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
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5 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Decrease in Parental Stress
Time Frame: 5 months
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Parent perceived general stress will be assessed using the Perceived Stress Scale.
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5 months
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Decrease in Parental Stress
Time Frame: 5 months
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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
Time Frame: 5 months
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Diurnal cortisol rhythm levels will be determined by obtaining samples of parents' saliva.
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5 months
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Parental Mental Health Improvement
Time Frame: 5 months
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The Center for Epidemiological Depression Studies Scale will be used to determine parental depressive symptoms.
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5 months
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Parental Mental Health Improvement
Time Frame: 5 months
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The Mental Health Continuum-Short Form will be used to measure parents' positive mental health symptoms.
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5 months
|
Improvement in Parental Feeding Behaviors
Time Frame: 5 months
|
Parental feeding behaviors will be assessed using The Child Feeding Questionnaire.
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5 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Ashley Butler, Ph.D, Baylor College of Medicine
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- H-37460
- 46486-I (Other Grant/Funding Number: Texas Children's Hospital Pediatric Pilot Award)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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