Obesity Clinical Trial
Official title:
Mood and Behavior Changes Among Overweight Adolescent Females
Verified date | November 2016 |
Source | University of Kentucky |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Observational |
The specific aims of this study are to document the co-existence of depression, low
self-esteem, and high-risk behaviors among overweight and at-risk for overweight female
adolescents; and decrease the prevalence of high-risk behaviors by improving depressive
symptoms/signs and self-esteem through weight management intervention strategies that
encourage long-term mental and physical well being. The proposed research will test the
following hypotheses:
- Overweight and at-risk for overweight female adolescents have poor self-esteem that may
mask depression and mediate high-risk behaviors; and
- Improved weight perception decreases participation in high-risk behavior secondary to
improved self-esteem and depression.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | September 2006 |
Est. primary completion date | September 2006 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 10 Years to 14 Years |
Eligibility |
Inclusion Criteria: - Girls 10 through 14 years of age who are in good general health and have a BMI in the 85th to 95th percentile or greater than the 95th percentile - Availability of a parent or guardian to ensure the child attends all monthly clinic visits and who will be available to attend the monthly educational sessions if the child is assigned to the intervention group Exclusion Criteria: - Cardiac or pulmonary conditions such as cystic fibrosis, congenital heart disease, or other conditions that would impair ability to do fitness testing - Physical challenges such as deformities that would impair ability to perform physical activities - Use of medications such as corticosteroids, seizure medication, or other central nervous system (CNS) medications that would interfere with daily physical activity |
N/A
Country | Name | City | State |
---|---|---|---|
United States | University of Kentucky | Lexington | Kentucky |
Lead Sponsor | Collaborator |
---|---|
University of Kentucky |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Decreased body mass index; increased physical activity | |||
Secondary | Improved self-esteem; improved depression scale score; decreased risk-taking behavior |
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