A Prospective Study Investigating the Effects of a Novel Weight Management Program

Overweight Clinical Trial

Official title:

A Prospective, Randomized, Blinded, Controlled Study Investigating the Effects of a Novel Body Weight Management Program Over 90-days and Weight Maintenance at One Year.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01875354
• Other study ID #: 13-PHX-01-NU-02
• Status: Completed
• Phase: N/A
• First received: June 5, 2013
• Last updated: April 3, 2017
• Start date: May 2013
• Est. completion date: November 2014

Study information

• Verified date: April 2017
• Source: Pharmanex
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to assess the safety and efficacy of a weight management program composed of dietary supplements and a reduced calorie eating program.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 141
• Est. completion date: November 2014
• Est. primary completion date: November 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Male or female 18-65 years of age at the time of informed consent

2. The ability to read, speak and understand the English language in order to complete the required paper informed consent, assessments and diary

3. Access to email and to a digital camera or camera phone

4. Willing and able to provide written informed consent

5. Willing and able to comply with the study restrictions, procedures and assessments and attend regularly scheduled clinic visits

6. Willing and able to accommodate being contacted by the study staff for telephone call visits, follow-up contacts, and study visit reminders

7. BMI is equal to or greater than 25 and less than or equal to 40 kg/m2

8. Use of effective method of contraception by females of childbearing potential 30-days before the screening visit and agree to continue to practice that acceptable method of contraception for the duration of her participation in the study

9. A resting normotensive blood pressure, as defined as a systolic blood pressure between 150-90 mmHg and a diastolic blood pressure of between 95-50 mmHg, at screening visit 1(A)

10. Willing to fast for at least 8 hours prior to the study procedures being performed that require fasting measurements

11. Willing and able to follow eating program and able to consume the study supplied Supplements, Placebos and shakes (which include whey and/or egg protein) on a daily basis. Subjects that are lactose intolerant will be considered ineligible

12. Only one member per household eligible to participate in the study

Exclusion Criteria:

1. A subject that has any Axis I Psychiatric disorders according to the DSM-IV criteria that would prevent the subject from being able to comply with study requirements and/or taking anti-psychotic medication

2. Diagnosed with insomnia and is chronically using prescribed or OTC insomnia medications

3. A self-reported chronic condition that may affect subject safety

4. An HbA1c of greater than or equal to 7.0%

5. Renal insufficiency as defined by a laboratory Glomerular Filtration Rate of less than 50 mL/min/1.73 m2

6. Chronically using glucocorticoid steroids

7. Currently pregnant, planning to become pregnant during the course of the study or is breastfeeding

8. Use of antihypertensive medication(s) for less than 90 days prior to screening

9. Diagnosed with any thyroid disorder or has a clinically significant out of range laboratory value (i.e. TSH, T3 Free, and/or T4 Free) value measured at screening

10. Known allergy or intolerance to any of the ingredients contained in the Novel Supplements, placebos or shakes (cow milk proteins)

11. Planned surgical procedure during the 365 day course of the study

12. Currently participating in another clinical research study or have done so within 30 days prior to the screening visit

13. Diagnosis of milk or egg intolerance

14. Participating in another weight loss program or using another weight loss product. Subjects may enroll if they are willing to stop the weight loss program they are currently on and/or washout of the product they are using. The appropriate washout will be reviewed with the investigator or medically qualified designee on a case by case basis

15. Fasting LDL-C greater than 190 mg/dL or triglycerides greater than 400 mg/dL.

16. Unwilling to discontinue consumption of green or black tea or green or black tea extracts beginning at the screening visit and after signing of the informed consent

17. Unwilling to discontinue use of over-the-counter and/or prescribed vitamin supplements except for: multivitamins, calcium, fish oil, vitamin C, vitamin D, vitamin E, zinc or iron

18. Plans to have plastic or reconstructive surgery or any other procedure that, in the opinion of the investigator, could influence body composition, at any time during the year long study

19. Unable to lay supine for at least 30 minutes

20. Cognitive impairment that would limit ability to understand or follow diet instructions and/or comply with the study protocol

Related Conditions & MeSH terms

• Overweight

Intervention

Dietary Supplement:
• Dietary Supplements and TR90 Eating Plan
Supplements to maintain muscle, assist in utilization of body fat, curb appetite, support positive willpower along with TR90 Eating plan. TR90 Eating Plan will consist of approximately 30 g high quality protein along with fruit, vegetables and complex carbohydrates
• Placebo and Low Fat Eating Plan

Locations

Country	Name	City	State
United States	Utah State University	Logan	Utah

Sponsors (2)

Lead Sponsor	Collaborator
Pharmanex	Utah State University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Determine the effect of a novel weight management program on body fat mass over 90 days.	Evaluate changes in body measurements (weight and BMI; arm, waist, hip, thigh, claf, and ankle circumferences) and body composition (fat mass, fat free mass, % body fat) by Dual Energy X-ray Absorptiometry (DEXA) scanner.	Days 0 and 90
Secondary	Determine the safety of novel weight management program (CBC, Comp. metabolic, lipid panel, heart rate, blood pressure and adverse events)		Throughout 1 year
Secondary	Evaluate changes in body measurements (weight and BMI; arm, waist, hip, thigh, claf, and ankle circumferences) and body composition (fat mass, fat free mass, % body fat) by Dual Energy X-ray Absorptiometry (DEXA) scanner.		throughout 1 year
Secondary	Determine subjective measurements of hunger and appetite from standardized questionnaires (IWQOL Hunger/Appetite and overall wellbeing)		Throughout 1 year
Secondary	Determine skin carotenoid (Biophotonic Scanner) measurement changes.	Biophotonic Scanner utilizes raman spectroscopy to determine skin carotenoid concentrations.	Throughout 1 year
Secondary	Evaluate the changes in metabolism and appetite hormone levels from the baseline visit to day 90.	Leptin, Insulin, Adiponectin, Pancreatic Polypeptide, gLP1, C-peptide, Glucagon, Resistin and HbA1c	Days 0 and 90
Secondary	Evaluate the changes in inflammatory markers from the baseline visit to day 90.	hsCRP, IL-6 and TNF Receptors 60 and 80	Days 0 and 90
Secondary	Evaluate the changes in gene expression from the baseline visit to day 90.	Full gene arrays will be made on peripheral blood mononuclear cells. The gene expression changes will be made at baseline and day 90. There will also be a comparison back to proteins (i.e. hormones and inflammatory markers).	Day 0 and 90
Secondary	Evaluate resting energy expenditure and substrate utilization from baseline to days 90, 180, and 365.	Resting metabolic rate (RMR)and substrate utilization (R-values to determine wheather subjects are utilizing more fats or carbohydrates to meet energy demands) will be measured by CPET Quark.	Days 0, 90, 80, and 365