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Effect of South Beach Diet (SBD™) Using SBD™ Products Compared to a Calorie-Restricted Diet in Women

M

Mondelez International

Status

Completed

Conditions

Overweight

Treatments

Behavioral: Calorie restricted diet with South Beach Diet™ Products
Behavioral: South Beach Diet™
Behavioral: Calorie Restricted Diet
Behavioral: South Beach Diet™ with South Beach Diet™ Products

Study type

Interventional

Funder types

Industry

Identifiers

NCT00932516
07SWHK-NONDIABETIC

Details and patient eligibility

About

The purpose of this study is to examine the effectiveness of the South Beach Diet™ and South Beach Diet™ products compared to a traditional calorie restricted diet.

Enrollment

248 patients

Sex

Female

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Female age 18 to 55 years
  2. Females of childbearing potential must agree to use a medically approved method of birth control and have a negative urine pregnancy test result
  3. Healthy as determined by laboratory results and medical history
  4. Waist circumference > 87 cm
  5. Stable weight defined as < 4.5 kg gained or lost in past 3 months
  6. Agreement to maintain current level of physical activity throughout the study
  7. Ability to comprehend and complete the questionnaires and forms
  8. Agreement to comply with study procedures, test article consumption and has access to a microwave oven
  9. Voluntary, written, informed consent to participate in the study

Exclusion criteria

  1. Pregnant, breastfeeding, or planning to become pregnant during the course of the trial
  2. Use of prescription or over the counter products known to effect weight including but not limited to the following: megestrol acetate; somatropin; sibutramine; orlistat; paroxetine; dextroamphetamine; methylphenidate; atomoxetine; quetiapine; olanzepine; risperidone, within 4 weeks of randomization and during the trial
  3. Alcohol use > 2 standard alcoholic drinks per day
  4. Significant cardiac history defined as a history of myocardial infarction (MI); coronary angioplasty or bypass graft(s); valvular disease or repair; unstable angina pectoris; transient ischemic attack (TIA); cerebrovascular accidents (CVA); congestive heart failure; or coronary artery disease (CAD)
  5. History of or current diagnosis of any cancer (except for successfully treated basal cell carcinoma) diagnosed less than 5 years prior to screening Subjects with cancer in full remission for more than 5 years are acceptable
  6. Uncontrolled hypertension defined as untreated systolic blood pressure > 160 mmHg and/or diastolic blood pressure > 100 mmHg
  7. Diabetes mellitus Type I or Type II
  8. Unstable renal and/or liver disease
  9. History of alcohol or drug abuse within the past year
  10. Unstable psychiatric disorder requiring hospitalization within the past 6 months
  11. Immunocompromised individuals such as subjects that have undergone organ transplantation or subjects diagnosed with human immunodeficiency virus (HIV)
  12. History of hemoglobinopathies such as sickle cell anemia or thalassemia, sideroblastic anemia
  13. Participation in another clinical research trial within 30 days prior to randomization and during the trial
  14. Significant abnormal liver function as defined as AST and/or ALT > 2 x ULN, and/or bilirubin > 2 x ULN
  15. Serum creatinine > 125 umol/L
  16. Anemia of any etiology defined as hemoglobin < 110 g/L
  17. Uncontrolled and/or untreated thyroid disorder
  18. Unstable medications (Dosage must be stable for 90 days prior to randomization)
  19. History of food allergies or sensitivities including lactose intolerance
  20. Vegetarians
  21. Cognitively impaired and/or unable to give informed consent
  22. Any other condition which in the Investigator's opinion may adversely affect the subject's ability to complete the study or its measures or which may pose significant risk to the subject

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

248 participants in 4 patient groups

South Beach Diet™ with SBD™ Products
Active Comparator group
Treatment:
Behavioral: South Beach Diet™ with South Beach Diet™ Products
South Beach Diet™ alone
Active Comparator group
Treatment:
Behavioral: South Beach Diet™
Calorie restricted diet w/ SBD™ Products
Active Comparator group
Treatment:
Behavioral: Calorie restricted diet with South Beach Diet™ Products
Calorie Restricted Diet alone
Active Comparator group
Treatment:
Behavioral: Calorie Restricted Diet

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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