Type of Study:

Interventional

Study Design:

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Outcome Measure:

BMI change at 6 month post assessment

Outcome Description:

Postpartum adolescents in the intervention group who are at risk for overweight (85th-94th percentile BMI) or are overweight (equal to or greater than the 95th percentile) at baseline will have a change in BMI with a lower absolute BMI at 6 month post assessment than those in the control group

Outcome Time Frame:

Baseline and 6 month post assessment

Safety Issue:

No

Principal Investigator

Debra Haire-Joshu, PhD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Washington University in St. Louis

Authority:

United States: Institutional Review Board

Study ID:

201105325

NCT ID:

NCT01617486

Start Date:

January 2007

Completion Date:

May 2009

Related Keywords:

• Obesity
• Obesity