OPTIFAST
Othermedically-supervised weight management program
NCT Number: NCT02635698
Compare percent change in loss of body weight between the OPTIFAST program and a food-based energy-deficit program
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Notify Me18 year–70 year
All sexes
Interventional
Not applicable
Alaska Premier Health, Anchorage, Alaska, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
medically-supervised weight management program
low-energy, low-fat diet
Time frame: 26 weeks
Percent change in body weight between Initial Visit/Baseline and 26 weeks
Time frame: 52 weeks
Percent change in body weight between Initial Visit/Baseline and 52 weeks
Time frame: 52 weeks
Percentage of subjects meeting short- and long-term weight loss goals
Time frame: 52 weeks
change in BMI in kg/m^2 from baseline to 52 weeks
Time frame: 52 weeks
Change in 10-year cardiovascular risk score (% likelihood to develop CVD in 10 years)
Société des Produits Nestlé (SPN)
Industry
Opti-WIN: Effectiveness of the Optifast Program Compared With a Reduced-energy Food Based Diet Plan on Body Weight
Acronym: Opti-WIN
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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