- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03781856
La Vida Buena Childhood Obesity Program
La Vida Buena (The Good Life) Evaluation: A Quasi Experimental Intervention of a Community Health Worker Led Family-based Childhood Obesity Program for Hispanic Children 5-8 Years of Age on the US-Mexico Border
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
La Vida Buena is a Mariposa project to educate children and families about healthy eating and exercise habits. The Health providers at Mariposa Nogales and Rio Rico clinics will refer children between 5-8 years old who are overweight or obese and their parents. Each child must participate with a parent or adult caregiver who is at least 18 years old. Before the program begins, the participant will attend an informational consent/registration session where they will be asked to sign a consent form for themselves and their child if they want to participate. The study will ask for certain information from each participant in order to determine if the program is working. Each family will respond to a questionnaire at three points: at the beginning of the program, three months after beginning the program, and six months after beginning the program, for a total of six months.
The questionnaire will include questions about fruit, vegetable and carbohydrate consumption, family behavior and habits regarding eating and exercise, moderate and vigorous physical activity, sedentary behavior, local foods and environment factors that impact the family. In addition, the child's weight will be measured at each time point.
Participation in La Vida Buena will take 6 months. At the Nogales site, participants will be invited to a series of weekly classes over the course of 8 weeks that are being offered by the Mariposa clinic related to child healthy weight, exercise and nutrition. At the Rio Rico site, participants will be offered one face to face educational session about child healthy weight with Mariposa staff. Participants will be scheduled for BMI measurements and questionnaires three months after initiating the program, as well as six months after initiating the La Vida Buena Program.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Arizona
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Nogales, Arizona, United States, 85621
- Mariposa Community Health Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 5 to 8 years of age
- Above the 85th percentile for obesity
- Accompanied by a parent or legal guardian.
Exclusion Criteria:
- Not between the ages of 5 and 8
- Not above the 85th percentile for obesity.
- Not accompanied by a parent or legal guardian.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: La Vida Buena Program
Administered in a group setting over the course of 8 weeks in a community setting.
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The intervention is series of interactive one hour weekly classes over the course of 8 weeks related to child healthy weight, exercise and nutrition.
Facilitated by community health workers, the classes are interactive and play-based and designed to engage both the child and accompanying parent or guardian in activities.
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|
Active Comparator: Brief educational session
Administered one on one or in a group setting in a one-hour session at the clinic
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A one hour session about nutrition and physical activity to address obesity facilitated by a community health worker
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
BMI
Time Frame: baseline to 6 months follow up
|
Weight and height measured at baseline, post intervention and 6 months.
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baseline to 6 months follow up
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Physical activity
Time Frame: baseline to 6 months follow up
|
Increased physical activity as measured by the International Physical Activity Questionnaire - Short Form
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baseline to 6 months follow up
|
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Fruit and vegetable consumption
Time Frame: baseline to 6 months follow up
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As measured by self reported servings per day or week with higher values considered to be a better outcome
|
baseline to 6 months follow up
|
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Simple carbohydrate consumption
Time Frame: baseline to 6 months follow up
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As measured by self report servings per day or week with lower values considered to be a better outcome
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baseline to 6 months follow up
|
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Family healthy habits
Time Frame: baseline to 6 months follow up
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As measured by the Family Nutrition and Physical Activity Tool designed to capture healthy family habits.
The adapted scale includes 16 items that are score from 1 to 4 that measure physical activity, sport participation, television viewing and video games for their negative influence on child hood obesity.
Total score ranges from 16 to 64 points, with an increased score being associated with positive outcomes.
There is not threshold or cutoff for the scale.
|
baseline to 6 months follow up
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Maia Ingram, University of Arizona
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
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
- 1710977008
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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