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Dietary Messages for Obesity
N/A
Waitlist Available
Led By Hollie Raynor, PhD, RD
Research Sponsored by The University of Tennessee, Knoxville
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Have a parent aged > 21 years with a BMI > 25
Children between ages 6-12 years
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline and 6 months
Awards & highlights
No Placebo-Only Group
Summary
This trial is looking at the effects of 3 different types of dietary messages on what parents and their children eat, and how it impacts their health.
Who is the study for?
This trial is for families with a child aged 6-12 within a healthy weight range and an overweight parent willing to attend meetings. Both must speak English and not plan to move during the study.
What is being tested?
The study tests three diet messages: increasing fruits and vegetables, reducing snack foods, or doing both. It aims to see how these messages affect what families eat and their health.
What are the potential side effects?
There are no direct side effects from participating in this dietary intervention trial; however, changes in diet may lead to temporary digestive adjustments.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My parent is over 21 years old and has a BMI over 25.
Select...
My child is between 6 and 12 years old.
Select...
My BMI is between the 5th and 85th percentile for my age and sex.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline and 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline and 6 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in Dietary intake
Secondary study objectives
Change in Anthropometrics
Change in Eating Pathology
Change in Obesogenic Home Food Availability
+3 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
3Treatment groups
Experimental Treatment
Group I: Increase ConditionExperimental Treatment1 Intervention
A parent and child will be encouraged to increase fruits and vegetables. Children will be encouraged to consume 1 cup/day and 1.5 cups/day of whole fruit, and 1.5 cups/day and 2 cups/day of vegetables for children aged 6 to 8 years and 9 to 12 years, respectively. Children will gradually work towards these goals. Parents will also work towards F\&V goals, with 2 cups/day of whole fruit and 2.5 cups/day of vegetables.
Group II: Increase + Decrease ConditionExperimental Treatment1 Intervention
Families will be encouraged to increase fruits and vegetables and decrease snack foods.
Group III: Decrease ConditionExperimental Treatment1 Intervention
In the Decrease Snack Foods condition participants will reduce intake of SFs (i.e., candy, cookies, cakes, ice cream, chips, nuts) to \< 3 servings/week (for children aged 6 to 12 years, the solid fats and added sugar energy limit is 840 kcals/week and the DECREASE goal will help with meeting this limit). Children and parents will gradually work towards meeting these goals and self-monitor these behaviors.
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Who is running the clinical trial?
The University of Tennessee, KnoxvilleLead Sponsor
86 Previous Clinical Trials
18,847 Total Patients Enrolled
18 Trials studying Obesity
7,392 Patients Enrolled for Obesity
Hollie Raynor, PhD, RDPrincipal InvestigatorUniversity of Tennessee
1 Previous Clinical Trials
20 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- My parent is over 21 years old and has a BMI over 25.My child is between 6 and 12 years old.My BMI is between the 5th and 85th percentile for my age and sex.My overweight/obese parent is willing to attend intervention meetings with me.
Research Study Groups:
This trial has the following groups:- Group 1: Increase Condition
- Group 2: Increase + Decrease Condition
- Group 3: Decrease Condition
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.