- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04252677
Health Literacy and Obesogenic Behaviors (HL-Squared)
Health Literacy as a Vehicle to Reduce Obesogenic Behaviors Among Adolescents: A Pilot Intervention
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The rates of pediatric obesity (~19%) and diabetes (0.24%) in the US are alarming and behaviors implicated in obesity and type 2 diabetes are highly prevalent. Approximately 69% and 73% of adolescents consume less than two fruits and vegetables daily respectively, while 53% engage in insufficient physical activity. These behaviors magnify adolescents' immediate and long-term risks for obesity and obesity-related chronic illnesses, as well as complicate the treatment of obesity-related chronic illnesses. Children and adolescents who are obese are four times more likely to be diagnosed with type 2 diabetes than normal weight children, with serious short and long-term consequences impacting quality of life. Reduced life expectancy is the future of America's youth if behavioral changes are not implemented to improve health and reduce the obesity burden. Reversing current national trends in obesity and type 2 diabetes require novel and sustainable prevention strategies to address children and adolescents' obesogenic behaviors.
Adolescence is marked by increased autonomy in decision-making, yet data suggest that adolescents are not equipped with all the skills to make effective health-related behavioral decisions. While health knowledge works in conjunction with motivation and behavioral skills to predict behavior, most existing adolescent interventions target these variables in isolation with modest success. Researchers have argued that health literacy (HL) - the ability to access, understand, and use health information to make informed health decisions - is a precursor to health knowledge and is necessary for translating health knowledge into behavior. Low HL among adults is associated with poor ability to interpret health messages, and results in reduced preventive health behaviors. Further, parent and adolescent HL is negatively related to adolescents' obesity status. Thus, while research on adding HL to existing behavior interventions to improve adolescents' obesity prevention behaviors is lacking, it is expected that the inclusion of HL into existing interventions will increase intervention effectiveness and positive behavior outcomes.
The long-term goal of this line of research is to reduce the incidence of obesity in adolescents and by extension reduce the risk for obesity-related chronic illnesses using interventions that address individual and contextual factors related to long-term health decision-making and behavior change. The goal of the proposed study is to examine the effect of adding a HL component to an obesity prevention intervention that addresses adolescents' obesogenic behavior-related health knowledge, motivation, and behavioral skills. The central hypothesis is adolescents receiving HL training as part of an obesity prevention intervention will have higher rates of prevention behaviors than those in the obesity prevention only condition. Study goals will be achieved through the following specific aims:
Aim 1: Modify successful components of existing obesity prevention interventions into an interactive digital platform with and without HL for acceptability and usability in adolescents.
Approach: Use successful components of existing interventions, our completed preliminary research, and our research teams' expertise to develop an interactive digital intervention including HL, and obesogenic behavior-related health knowledge, motivation, and behavioral skills. Assess and modify the intervention for usability and acceptability among 14-16-year-olds through an iterative process.
Aim 2: Determine if the addition of HL training to an interactive digital obesity prevention intervention will improve adolescents' obesity prevention behaviors over the obesity intervention alone.
Hypothesis: Adolescents in the obesity prevention plus HL intervention will have higher rates of obesity prevention behaviors at posttest and follow-up compared to the obesity prevention only group.
Approach: Conduct a two-arm randomized controlled trial (RCT) intervention (obesity prevention only, obesity prevention/HL) and estimate the intervention's effects on obesogenic behaviors. Adolescents (n = 36; 14-16-year-olds) will be randomly assigned to each condition (18/condition). Conduct pretest, posttest, and 1- month assessments of HL, obesogenic behaviors, and obesogenic behavior-related motivation, behavioral skills, and knowledge.
Outcomes: Intervention completion will result in effect size estimates of improvements in obesity prevention behaviors, health knowledge, motivation, and behavioral skills for both groups with greater improvements for the HL group at posttest and follow-up. The obesity prevention/HL intervention group will also have higher HL at posttest and follow-up. Retention, recruitment, completion and treatment fidelity rates will be established.
Innovation & Impact: This study incorporates HL, an understudied but potentially critical factor in adolescents' health behaviors. The intervention will be developed and implemented in a digital format which will increase reach and impact. This is the first study examining the effect of including HL in adolescents' obesity prevention interventions. This study sets the groundwork for a full scale, RCT to assess the benefit of HL training added to an obesity prevention intervention to address adolescents' obesogenic behaviors.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
New York
-
New York, New York, United States, 10027
- CUNY Graduate School of Public Health and Health Policy
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Adolescents 13-16 years old at time of enrollment (may turn age 17 during the study
- Must have parental consent
- All weight classifications
Exclusion Criteria:
- Adolescents younger than 13 years or older than 16 years at time of enrollment
- No parental consent
- Medical conditions preventing engagement in physical activity
- Medical conditions resulting in extremely restricted diets (e.g., ketogenic diet)
- Already participating in an intervention related to healthy eating, physical activity and/or obesity prevention or treatment
Study Plan
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 |
|---|---|
|
Active Comparator: Vaping and Obesity Prevention Only
Obesity prevention and vaping
|
This intervention includes content specific to obesity behaviors-related health information, motivation, and behavioral skills.
|
|
Experimental: Health Literacy and Obesity Prevention
Obesity prevention and health literacy (HL).
|
This intervention includes content specific to obesity behaviors-related health information, motivation, and behavioral skills.
This intervention includes content specific to improving health literacy.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Improvement in Participants' Healthy Eating Behaviors as Assessed by the Dietary Screener Questionnaire and the National Youth Physical Activity and Nutrition Study
Time Frame: 5 months
|
Percent of participants improved healthy eating (e.g., fruits and vegetables) behaviors
|
5 months
|
|
Reductions in Participants' Unhealthy Eating Behaviors as Assessed by the Dietary Screener Questionnaire and the National Youth Physical Activity and Nutrition Study
Time Frame: 5 months
|
Percent of participants reduce unhealthy eating (sugary and salty foods, junk foods) behaviors
|
5 months
|
|
Improvements in Participants' Physical Activity as Assessed by the Youth Activity Profile
Time Frame: 5 months
|
Percent of participants increase number of days with 60 minutes of more of physical activity
|
5 months
|
|
Improvements in Participants' Physical Activity as Assessed by the Godin and Shephard Leisure-Time Physical Activity Questionnaire
Time Frame: 5 months
|
Percent of participants in weekly leisure activity score
|
5 months
|
|
Reductions in Participants' Sedentary Activity as Assessed by the Youth Activity Profile
Time Frame: 5 months
|
Percent of participants with increase in number of days with less than 2 hours of sedentary behaviors
|
5 months
|
|
Reduction in Participants' Sugar-sweetened Beverage Consumption as Measured by the Dietary Screener Questionnaire and the National Youth Physical Activity and Nutrition Study
Time Frame: 5 months
|
Percent of participants with reduced sugar-sweetened beverage intake
|
5 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Participants' Functional Health Literacy Will be Assessed Using the Assessments of Adolescent Health Literacy Scales
Time Frame: 5 months
|
Percentage of participants with maintenance (at max score) or improvement in objective measure of reading and numeracy skills for health
|
5 months
|
|
Participants' Interactive Health Literacy Assessed Using the Assessments of Adolescent Health Literacy Scales
Time Frame: 5 months
|
Percentage of participants with maintenance at max score or improvement in objective assessment of interactive health literacy
|
5 months
|
|
Participants' Critical Health Literacy Will be Assessed Using the Assesments of Adolescent Health Literacy Scales
Time Frame: 5 months
|
Percentage of participants with maintenance or improvement in objective measure of social skills and critical thinking for health
|
5 months
|
|
Participants' Media Health Literacy Will be Measured Using the Adolescent Media Health Literacy Scale and eHeals
Time Frame: 5 months
|
Percentage of participants with maintenance or improvement in objective measure of media literacy for health
|
5 months
|
|
Participants' Overall Health Literacy Will be Assessed Using the Assessments of Adolescent Health Literacy Scales
Time Frame: 5 months
|
Percentage of participants with maintenance or improvement in objective measure of three core components of health literacy (functional, interactive, critical)
|
5 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Sasha A Fleary, PhD, City University of New York
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
Keywords
Additional Relevant MeSH Terms
- Nutrition Disorders
- Overnutrition
- Body Weight
- Overweight
- Pathological Conditions, Signs and Symptoms
- Nutritional and Metabolic Diseases
- Signs and Symptoms
- Obesity
- Pediatric Obesity
- Motor Activity
- Health Behavior
- Behavior
- Health Services
- Health Care Facilities Workforce and Services
- Preventive Health Services
- Health Education
- Consumer Health Information
- Health Literacy
Other Study ID Numbers
- HLSQUARED01
- R21DK117345 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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