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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00067600
Date of registration: 25/08/2003
Primary sponsor: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Public title: Improving Bone Health in Adolescent Girls: The Youth Osteoporosis and Understanding Total Health (YOUTH) Study
Scientific title: Lifestyle Changes to Increase Bone Density in Teen Girls
Date of first enrolment: August 2000
Target sample size: 228
Recruitment status: Active, not recruiting
URL:  http://clinicaltrials.gov/show/NCT00067600
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Prevention  
Countries of recruitment
United States
Contacts
Name:   Lynn L DeBar, PhD, MPH
Address: 
Telephone:
Email:
Affiliation:  Kaiser Permanente
Key inclusion & exclusion criteria

Inclusion Criteria

- High school freshman or sophomore

- Body mass index (BMI) from 16 through 23

- Member of Kaiser Permanente Northwest Health Plan

- Parent or guardian willing to participate

Exclusion Criteria

- Co-morbidity requiring a specific diet

- Medication which contraindicates consuming a high-fiber diet

- Life-threatening disease or other condition that would interfere with study
participation

- Current or past medically or self-diagnosed eating disorder

- Current behaviors consistent with eating-related disorder

- Pregnancy

- Diagnosis of psychological disorder or difficulty within the past year



Age minimum: 14 Years
Age maximum: 16 Years
Gender: Female
Health Condition(s) or Problem(s) studied
Osteoporosis
Intervention(s)
Behavioral: Diet with increased fruits, vegetables, and calcium
Behavioral: Increased high impact activity and resistance training
Primary Outcome(s)
Secondary Outcome(s)
Secondary ID(s)
R01HD37744
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
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