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Completed

NCT Number: NCT02635698

Effectiveness of the Optifast Program Compared With a Reduced-energy Food Based Diet Plan on Body Weight

Compare percent change in loss of body weight between the OPTIFAST program and a food-based energy-deficit program

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Alaska Premier Health, Anchorage, Alaska, United States

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Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult males and females between 18 and 70 years
  • Obese (BMI > 30 kg/m2 and 55 kg/m2)
  • Non-smokers or smoking cessation > 6 months
  • < 14 alcoholic beverages per week
  • Willing and able to give informed consent

Exclusion criteria

  • Active participation in any weight loss program within previous 3 months
  • Weight changes of > 5% body weight within previous 3 months
  • Participated in an Optifast program within prior 5 years
  • Prior bariatric surgery or liposuction
  • Use of any medication prescribed for weight loss in the past 3 months
  • Current major disease or GI disease that is poorly controlled (Crohn's, ulcerative colitis)
  • Type 1 DM
  • Current ESRD
  • Current COPD
  • Any major or active hepatic disease requiring inpatient or outpatient treatment
  • History of acute pancreatitis in the past year
  • Active cancer treatment in the past 2 years other than non-malignant skin cancers
  • Uncontrolled hypertension (Blood pressure 160/100 or greater)
  • Hemoglobin A1c > 10%
  • Recent CV event in past 6 months
  • Pregnancy, childbirth, or nursing within prior 6 months
  • Eating Attitudes Test (EAT-26) > 30
  • Current major depressive disorder with Center for Epidemiological Studies Depression Scale-Revised (CESD-R) score > 16
  • Schizophrenia, history of bipolar disorder
  • Recent hospitalization for psychiatric illness in past 6 months
  • Dependence on alcohol or sedative-hypnotic drugs
  • Intolerance or allergy to Optifast product
  • Unable to read/speak English
  • Orthopedic limitation preventing participation in regular physical activity
  • Untreated thyroid disease, abnormal TSH, non on stable dose of hormone replacement for hyperthyroidism
  • Major surgery defined as any surgical procedure that might require prolonged convalescence or limit participation in the program in any way
  • Inability to complete the 7-day run-in satisfactorily

Treatment and study plan

OPTIFAST

Other

medically-supervised weight management program

Food-Based

Other

low-energy, low-fat diet

Primary outcomes

  1. Percent weight change

    Time frame: 26 weeks

    Percent change in body weight between Initial Visit/Baseline and 26 weeks

  2. Percent weight change

    Time frame: 52 weeks

    Percent change in body weight between Initial Visit/Baseline and 52 weeks

Secondary outcomes

  1. Ability to meet weight goals

    Time frame: 52 weeks

    Percentage of subjects meeting short- and long-term weight loss goals

  2. Change in anthropometrics

    Time frame: 52 weeks

    change in BMI in kg/m^2 from baseline to 52 weeks

  3. Change in cardiometabolic outcomes

    Time frame: 52 weeks

    Change in 10-year cardiovascular risk score (% likelihood to develop CVD in 10 years)

Sponsors and collaborators

Lead sponsor

Société des Produits Nestlé (SPN)

Industry

Collaborators

  • TKL Research, Inc.

Registry information

Official study title

Opti-WIN: Effectiveness of the Optifast Program Compared With a Reduced-energy Food Based Diet Plan on Body Weight

Acronym: Opti-WIN

Important dates

Study start
2015
Primary completion
2017
Study completion
2017
First posted
Dec 21, 2015
Registry last updated
Nov 13, 2017

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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