Research Study of Nutritional Methods to Reduce Body Fat Percentages in Overweight and Obese Populations
The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified May 2007 by Central FITT, Inc.
Recruitment status was: Recruiting
Information provided by:
Central FITT, Inc
First received: June 15, 2007
Last updated: July 2, 2007
Last verified: May 2007
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:
- FREE Nutritional Services will be provided to eligible participants, which normally have a business value of between $165.00 and $195.00.
- 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.
Procedure: Non-Personalized Meal Planning
Procedure: Personalized Meal Planning and Dietetic Consultation
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind
Primary Purpose: Health Services Research
||Comparison of Body Fat Reduction in Overweight and Obese Subjects Utilizing Personalized Low-Fat Meal Plans vs. Non-Personalized Low-Fat Meal Plans.
Primary Outcome Measures:
- Pre and Post-Bioelectrical Impedance Body Fat Analysis [ Time Frame: 2 months ]
| Estimated Enrollment:
| Study Start Date:
| Estimated Study Completion Date:
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.
|Ages Eligible for Study:
||25 Years to 45 Years (Adult)
|Genders Eligible for Study:
|Accepts Healthy Volunteers:
- 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
- Individuals with the following health conditions:
- Food allergies
- Food intolerances
- Debilitating joint conditions such as Degenerative Joint Disease (DJD) and Degenerative Disk Disease (DDD)
- Diabetes Mellitus receiving insulin therapy
- Kidney problems
- 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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study.
To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below.
For general information, see Learn About Clinical Studies.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00487344
|Central FITT Inc
|Edmond, Oklahoma, United States, 73013 |
Central FITT, Inc
||Judith Brooks, Phd
||Eastern Michigan University CHHS Thesis Committee
||Anahita Mistry, PhD
||Eastern Michigan University-CHHS Thesis Committee
History of Changes
|Other Study ID Numbers:
|Study First Received:
||June 15, 2007
||July 2, 2007
||United States: Institutional Review Board
Keywords provided by Central FITT, Inc:
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on December 02, 2016
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