Black Adolescent & Entertainment Study
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| ClinicalTrials.gov Identifier: NCT03537755 |
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Recruitment Status : Unknown
Verified May 2018 by Henry M. Jackson Foundation for the Advancement of Military Medicine.
Recruitment status was: Recruiting
First Posted : May 25, 2018
Last Update Posted : May 25, 2018
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| Condition or disease | Intervention/treatment |
|---|---|
| Obesity, Childhood | Other: Observation |
| Study Type : | Observational |
| Estimated Enrollment : | 120 participants |
| Observational Model: | Case-Only |
| Time Perspective: | Cross-Sectional |
| Official Title: | The Effect of Food Marketing and Attentional Biases on Eating Behaviors in African American Adolescent Girls |
| Actual Study Start Date : | June 6, 2017 |
| Estimated Primary Completion Date : | December 31, 2018 |
| Estimated Study Completion Date : | December 31, 2018 |
- Other: Observation
Examine thoughts and behaviors
- Total energy consumption [ Time Frame: Day 1 ]Total energy consumption from a laboratory test meal
- Macronutrient intake [ Time Frame: Day 1 ]Total energy intake from fat, sugar, and sodium
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 12 Years to 17 Years (Child) |
| Sexes Eligible for Study: | Female |
| Gender Based Eligibility: | Yes |
| Gender Eligibility Description: | Self-reported female |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Probability Sample |
Inclusion Criteria:
- Female,
- Self-identify as African American or Black,
- 12 to 17 years of age at the start of the study,
- Presence of obesity by virtue of a body mass index (BMI) ≥ 95th percentile for age and sex or non-overweight by virtue of a BMI of at least the5th percentile, but below the 85th percentile, for age and sex,118 and
- English speaking.
Exclusion Criteria:
- Reports of the presence of a major chronic medical illness: renal, hepatic, gastrointestinal, endocrinologic (e.g., Cushing syndrome, hyper- or hypothyroidism), hematological problems or pulmonary disorders (other than asthma not requiring continuous medication),
- Individuals who self-report major depressive disorder, psychoses, current substance or alcohol use disorder, or any other psychiatric disorder that, in the opinion of the investigators, would impede competence or compliance or possibly hinder completion of the study.
- Current, regular use of prescription medications that affect appetite, mood, or body weight: currently prescribed serotonin re-uptake inhibitors (SSRIs), neuroleptics, tricyclics, stimulants, or any other medication known to affect appetite, mood, or body weight. Oral contraceptive use will be permitted, provided the contraceptive has been used for at least two months before the study visit,
- Failure to provide a rating of 6 or more on at least 50% of food items on the Food Preferences Questionnaire (Appendix F); exceptions may be given for restrictions due to religious practices or food allergies, if food items can be replaced with items of equivalent macronutrient content.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03537755
| Contact: Omni Cassidy, M.S. | 301-295-0581 | BAEStudy@usuhs.edu |
| United States, Maryland | |
| Uniformed Services University of the Health Sciences | Recruiting |
| Bethesda, Maryland, United States, 20814 | |
| Responsible Party: | Henry M. Jackson Foundation for the Advancement of Military Medicine |
| ClinicalTrials.gov Identifier: | NCT03537755 |
| Other Study ID Numbers: |
1F31MD010675-01 ( U.S. NIH Grant/Contract ) |
| First Posted: | May 25, 2018 Key Record Dates |
| Last Update Posted: | May 25, 2018 |
| Last Verified: | May 2018 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Pediatric Obesity Obesity Overnutrition |
Nutrition Disorders Overweight Body Weight |

