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Research Study of Nutritional Methods to Reduce Body Fat Percentages in Overweight and Obese Populations

Comparison of Body Fat Reduction in Overweight and Obese Subjects Utilizing Personalized Low-Fat Meal Plans vs. Non-Personalized Low-Fat Meal Plans.

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00487344
Enrollment
32
Registered
2007-06-18
Start date
2007-06-30
Completion date
2007-11-30
Last updated
2007-07-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

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Brief summary

The purpose of this study is to compare the use of personalized low-fat meal plans vs. non-personalized low-fat meal plans and the results in body fat reduction in overweight and obese subjects 25 to 45 years of age. Compensation to Eligible Participants: 1. FREE Nutritional Services will be provided to eligible participants, which normally have a business value of between $165.00 and $195.00. 2. Each eligible participant will receive compensation for mileage directly related to this study up to 35 miles at the 2007 IRS Business Mileage Reimbursement Rate for medical purposes of $0.20 per mile. This compensation will be provided to each eligible participant in the form of a complimentary Wal-mart Gift Card in the amount of $7.00, contingent upon his or her completion in the study.

Detailed description

Study Rationale: This experiment on the effect that the use of personalized low-fat meal plans has on body fat reduction is important for several reasons. First, the details of this research study may equip the public with knowledge to select quality nutrition programs for weight loss responsibly. Second, it may encourage the wellness and fitness community to reconsider the practice of providing clientele with non-personalized meal plans for weight loss, which are not usually designed by accredited dietetic professionals. Third, this study may benefit dietetic professionals by opening the lines of communication between the wellness community and the dietetic community regarding standards of care, and protecting the public by dispelling harmful and erroneous nutrition advice.

Interventions

PROCEDURENon-Personalized Meal Planning
PROCEDUREPersonalized Meal Planning and Dietetic Consultation

Sponsors

Central FITT, Inc
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE

Eligibility

Sex/Gender
ALL
Age
25 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Between 25 to 45 years of age * Classified as overweight or obese with body mass index (BMI) measurement between 25 and 50 * Limited to minor chronic health

Exclusion criteria

* Individuals with the following health conditions: * Food allergies * Food intolerances * Cancer * Debilitating joint conditions such as Degenerative Joint Disease (DJD) and Degenerative Disk Disease (DDD) * Diabetes Mellitus receiving insulin therapy * Kidney problems * Menopause * Polycystic ovarian syndrome (PCOS) * Currently pregnant or breast feeding * Using diuretics, chromium, and/or diet pills * Participants must: * Live in the following Oklahoma Counties: * Canadian, Cleveland, Logan, Lincoln, Oklahoma, and Pottawatomie * Will to travel to Edmond and Oklahoma City, Oklahoma

Design outcomes

Primary

MeasureTime frame
Pre and Post-Bioelectrical Impedance Body Fat Analysis2 months

Countries

United States

Contacts

Primary ContactStacy D Buzan, MS
oktrial@yahoo.com405-503-2759
Backup ContactMichael Buzan, MS
centralfitt@sbcglobal.net405-503-2758

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026