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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01087346
Other study ID # 100076
Secondary ID 10-HG-0076
Status Completed
Phase N/A
First received
Last updated
Start date November 19, 2010
Est. completion date July 12, 2019

Study information

Verified date February 15, 2024
Source National Institutes of Health Clinical Center (CC)
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Summary: - A few studies have explored the effects of providing parents with health information about their children. However, more information is needed about the relationship between awareness of health information and changes in behavior. This study will investigate the impact of health information on choices that parents make about food for their children. - Mothers and fathers with a biological child between the ages of 3-7 years old may be eligible for this study. Participants are recruited from the Washington, DC metropolitan area. - In this study, before visiting the research center, participants will answer online questionnaires about their children's health and eating habits and their own health and eating habits. - At the research center, participants will use a virtual reality model of a buffet to make food choices for their children. Participants will be introduced to the computer-based virtual buffet scenario as a training session to prepare for using the buffet during the experimental context. While in the virtual environment, participants wear a virtual reality helmet that allows them to see the virtual buffet scenario. - After the training session, participants will watch an interactive computer presentation about a health topic. - Participants will then visit the virtual buffet scenario again for the formal session, and will choose a virtual lunch meal for their child as before. - At the end of their visit, participants will complete post-test questionnaires about their experiences during the experiment and other research-related information. - Participants will be asked to complete a follow-up questionnaire online a week after their visit - The total time for the study visit is approximately 90 minutes. The participants children will not be asked to take part in the study. Eligibility: - Men and Women at least 18 years of age who have a biological child between the ages of 3 and 7 who has no major diet-related health conditions, developmental delays, or disabilities. You may not take part in the study if you have a history of seizures and/or are pregnant.


Description:

Purpose This study will investigate the impact of health information on choices that parents make about food for their children. Participants will use a virtual reality model of a buffet to make food choices. Mothers and fathers with a biological child between the ages of 3-7 years old may be eligible for this study. Participants are recruited from the Washington, DC metropolitan area. Study participants will complete THREE sets of surveys and one task. Participants will complete a web-based survey before coming in for a study appointment. When participants arrive for their appointment, they will watch an interactive presentation on health information. Next, participants will interact in a virtual reality environment and will be asked to select virtual lunch for their child from a buffet. While in the virtual environment, a participant wears a head-mounted virtual reality headset that allows him/her to see elements of the environment. Participants will complete an additional computer-based survey. Finally, participants will be asked to complete an online questionnaire a week following their visit. The total time for the study visit is approximately 90 minutes. The participants children will not be asked to take part in the study. Detailed Description This study will investigate issues around the impact of health information on choices that parents make about food for their children. Participants will perform tasks that include completing computer-based surveys, watching an interactive computer-based presentation about health information, participating in a virtual reality model by selecting virtual lunch for their children from a buffet, and completing a computed-based exit survey. As part of the study, participants will wear a virtual reality helmet and be immersed in a buffet where they will select virtual lunch for their child. For this study, we are only recruiting men and women that have a biological child between the ages of 3-7 years old. You may not take part in the study if you have a history of seizures and/or are pregnant.


Recruitment information / eligibility

Status Completed
Enrollment 1148
Est. completion date July 12, 2019
Est. primary completion date July 12, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility - INCLUSION CRITERIA : Study 1: All participants will be healthy adult women over the age of 18 (though in practice the age range is likely to be constrained naturally by the required age of the index child). 1. having a self-reported body mass index of greater than or equal to 25 2. having some amount of familiarity with their family health history 3. having a biological child between the ages of 4 and 5 inclusive, who lives in the same household at least 1 day out of the past 30 days, and who has no major food allergies or diet-related health conditions, developmental delays, or disabilities 4. having the ability to read and write in English 5. being able to come to the NIH Clinical Center for one visit EXCLUSION CRITERIA: 1. having a vestibular or seizure disorder; 2. having a high propensity for motion sickness; 3. known pregnancy; (4) uncorrected low vision or hearing; (5) inability to complete tasks in the virtual environment; (6) past or current history of eating disorder; (7) NHGRI employees Study 2: INCLUSION CRITERIA: All participants will be healthy adults over the age of 18 (though in practice the age range is likely to be constrained naturally by the required age of the index child). 1. having a self-perception of being overweight 2. having a biological child between the ages of 3 and 7 inclusive (of any weight), who has no food allergies to buffet items (e.g., dairy, wheat, fruit) or diet-related health conditions, developmental delays, or disabilities that would severely limit food choices on the virtual buffet and who does not have a vegan or gluten-free diet 3. self-reporting that the parent is responsible for feeding to the child to criterion 4. having the ability to read and write in English 5. being able to come to the NIH Clinical Center for one visit EXCLUSION CRITERIA: 1. having a vestibular or seizure disorder 2. having a high propensity for motion sickness 3. known pregnancy 4. uncorrected low vision or hearing 5. inability to complete tasks in the virtual environment 6. past or current history of eating disorder 7. NHGRI employees 8. having another household member or another biological parent of their index child having participated in the study 9. women who report being pregnant

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Reading Information
Reading information about risk factors for obesity among children

Locations

Country Name City State
United States National Institutes of Health Clinical Center Bethesda Maryland

Sponsors (1)

Lead Sponsor Collaborator
National Human Genome Research Institute (NHGRI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary The number of calories selected for participant's index child in a virtual buffet food selection task The number of calories selected for participant's index child in a virtual buffet food selection task 1 visit
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