- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01156402
Childhood Obesity Prevention Program for Hispanics
May 5, 2016 updated by: Meharry Medical College
Culturally-Appropriate Childhood Obesity Prevention Program for Hispanic Families
The purpose of this study is to evaluate the efficacy of a culturally-appropriate childhood obesity intervention with Hispanic families.
The program aims at preventing childhood obesity by targeting parents to address nutrition, physical activity, and sedentary behaviors in their children.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Childhood obesity has been ranked as a critical public health threat in the U.S. due to the increasing prevalence of obesity among children over the past three decades.
Childhood obesity poses both intermediate and long-term health risks, as well as considerable economic costs.
While this epidemic affects all socioeconomic levels, certain racial/ethnic groups are disproportionately affected, including Hispanics.The long-term goal of the current research is to contribute to the reduction of racial/ethnic disparities in obesity and obesity-related outcomes among Hispanics by testing a childhood obesity prevention program that has been culturally tailored for the Hispanic population through a participatory process.
This developmental community-based participatory research (CBPR) project is a collaborative community-academic partnership between Meharry Medical College (MMC), Tennessee State University-Center for Health Research (TSU-CHR), and a grassroots community-based organization called Progreso Community Center (PCC).
The Childhood Obesity Study is designed to evaluate two programs for Hispanic children ages 5 to 7 and their parents.
One program focuses on nutrition and physical activity (based on NIH's "We Can!" program), and a parallel program focuses on oral health (developed by TSU's Dental Hygiene Program).
Upon enrollment in the Study, parents and children will respond to an initial interview involving body measurement and questionnaire.
Families will be given physical activity monitor to be worn for 7 days and randomly assigned to one of two groups.
The families assigned to the Nutrition and Physical Activity Program will attend eight (8) bi-weekly classes (one every two weeks for four months) dealing with nutrition and physical activity.
In the Oral Health Program families will attend 4 monthly classes (once a month for four months).
These sessions deal with ways to take care of children's teeth and oral health.
In addition, these families will have the opportunity to sign up for a free dental cleaning and assessment at the Dental Hygiene Clinic at Tennessee State University.
Study Type
Interventional
Enrollment (Actual)
319
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Tennessee
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Nashville, Tennessee, United States, 37208
- Meharry Medical College
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Nashville, Tennessee, United States, 37203
- Vanderbilt University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
5 years to 8 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
Children:
- 5-7 year-old female or male of Hispanic origin (identified by parent)
- resident of Davidson County or adjacent counties
- ≥25th percentile of age- and sex-specific BMI (CDC growth charts) or one parent/caregiver with BMI ≥ 25 kg/m2
- More than one child may enroll per family
Parents:
- Hispanic origin (self-identified)
- Spanish speaker
- adult age 18 or older
- parent of at least one eligible child
- Only one parent per family may enroll as a study participant and respond to questionnaires
Exclusion Criteria:
Children:
- BMI ≥ 35 kg/m2
- Medical conditions affecting growth
- Conditions limiting participation in the interventions or measurements
- Taking medications affecting growth
- No consent or inability to understand informed consent
- Incomplete or missed baseline assessments
- Plan to move from geographic area within the next 12 months.
Parents:
- No exclusions
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Active Intervention: Obesity Prevention
|
The active intervention was adapted from the We Can! parent intervention to be culturally-appropriate for Hispanic families of children ages 5-7.
The tailored intervention is based on Social Cognitive Theory and Behavioral Choice Theory to provide parents and children with cognitive and behavioral skills to enable change in the target behaviors, and to encourage them to practice using these skills to strengthen their perceived competence in using these behaviors effectively.
|
|
Experimental: Alternative Intervention/control: Oral Health
|
The active intervention was adapted from the We Can! parent intervention to be culturally-appropriate for Hispanic families of children ages 5-7.
The tailored intervention is based on Social Cognitive Theory and Behavioral Choice Theory to provide parents and children with cognitive and behavioral skills to enable change in the target behaviors, and to encourage them to practice using these skills to strengthen their perceived competence in using these behaviors effectively.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Body Mass Index (BMI)-for-age percentile
Time Frame: one year
|
one year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Child eating behaviors
Time Frame: One year
|
One year
|
|
Child physical activity (accelerometers)
Time Frame: One year
|
One year
|
|
Parenting strategies
Time Frame: One year
|
One year
|
|
parent physical activity
Time Frame: one year
|
one year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2010
Primary Completion (Actual)
November 1, 2013
Study Completion (Actual)
May 1, 2016
Study Registration Dates
First Submitted
June 14, 2010
First Submitted That Met QC Criteria
July 1, 2010
First Posted (Estimate)
July 2, 2010
Study Record Updates
Last Update Posted (Estimate)
May 6, 2016
Last Update Submitted That Met QC Criteria
May 5, 2016
Last Verified
May 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 030425PC062 03 (Meharry IRB)
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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