Weight Loss
Conditions
Brief summary
Determine the effects of an 8-week weight loss intervention.
Detailed description
The purpose of this study is three-fold: 1) Determine whether an 8-week, patient-centered, weight loss intervention can be successfully implemented in overweight, college-age females for promotion of weight loss and prevention of weight regain at 8-weeks, three months, and six months follow-up; 2) Determine the effects of the intervention on established markers of calorie restriction, energy expenditure and body composition; 3) Determine the effects of a liquid meal on physiological and subjective markers of hunger and satiety from pre- to post- 8wk intervention in the intervention group vs control group.
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
* Females age 18-25years * Body Mass Index 25.0 to 29.9 kg/m2 (overweight) * Agree to receive frequent contacts from investigators and communicate with program staff for up to 6 months * Willing to measure blood glucose via finger prick test three to eight times per day for two weeks * Able to give written informed consent * Able to comply with study procedures
Exclusion criteria
* Unable or unwilling to give informed consent * Travel plans that do not permit participation * Pregnant or planning on becoming pregnant during the 6 months of participation in the study * Weight loss or gain exceeding 5% of body weight in the past 3 months * Current participation in a weight loss program * Diagnosis of mental disorder or chronic disease * History of eating disorder such as anorexia nervosa, bulimia nervosa, or binge eating disorder (unless approved by program staff) * History of surgery or procedure that could affect swallowing or digestion * Any person who is on a medically prescribed diet * Any current supplement use other than a daily multivitamin * Any current metabolic medication use other than birth control * Any bleeding disorders or blood clotting problems * Anyone who has donated blood or plasma in the last 20 days * Any tobacco or illicit drug users * Anyone who has allergies to any of the components of the liquid meal
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Body weight | 18 months |
Countries
United States