Recruiting

Observational Study

Sponsor:

Henry M. Jackson Foundation for the Advancement of Military Medicine

Code:

NCT03537755

Conditions

Obesity, Childhood

Eligibility Criteria

Sex: Female

Age: 12 - 17

Healthy Volunteers: Accepted

Interventions

Observation

Study Details

Brief summary:

The study is being conducted to obtain adolescent girls' thoughts and opinions on relationship and communication styles are shown on television.

Conditions

Obesity, Childhood

Study ID

NCT03537755

Start date

Jun 6, 2017

Status verified date

May, 2018

Completion date

Dec 31, 2018

Anticipated

Primary completion date

Dec 31, 2018

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Female

Age: 12 - 17

Healthy Volunteers: Accepted

Inclusion Criteria:

1. Female,
2. Self-identify as African American or Black,
3. 12 to 17 years of age at the start of the study,
4. 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
5. English speaking.

Exclusion Criteria:

1. 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),
2. 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.
3. 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,
4. 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.

Study Design

Enrollment

120 participants

Anticipated

Interventions and Outcome Measures

Interventions

Observation

Examine thoughts and behaviors

Primary outcome measure

  • Total energy consumption [ Time Frame: Day 1 ]
  • Macronutrient intake [ Time Frame: Day 1 ]

Central Contacts and Locations

Central contacts

Locations

Uniformed Services University of the Health Sciences

Recruiting

Bethesda, Maryland, United States, 20814

More Information

Sponsor

Henry M. Jackson Foundation for the Advancement of Military Medicine

Last update posted

May 25, 2018

Last verified

May, 2018

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Henry M. Jackson Foundation for the Advancement of Military Medicine on 2018-05-25.