The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jun. 17, 1997

Filed:

Jun. 06, 1995
Applicant:
Inventors:

Allen Chait, Seattle, WA (US);

Dan Hatton, Portland, OR (US);

R Brian Haynes, Dundas, CA;

Chor San Khoo, Mt. Laurel, NJ (US);

Penny Kris-Etherton, State College, PA (US);

R David Macnair, King of Prussia, PA (US);

David McCarron, Portland, OR (US);

Jill Metz, Portland, OR (US);

Suzanne Oparil, Birmingham, AL (US);

Xavier Pi-Sunyer, New York, NY (US);

Larry Resnick, West Bloomfield, MI (US);

Judith S Stern, Lafayette, CA (US);

Paula J Ziegler, Cherry Hill, NJ (US);

Assignee:

Campbell Soup Company, Camden, NJ (US);

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
A61K / ;
U.S. Cl.
CPC ...
424439 ; 424400 ;
Abstract

The invention is a method for determining the effectiveness of a diet program for administration to a patient having at least one diet-responsive condition. The method includes the steps of selecting a plurality of patients, each having at least one diet-responsive condition; identifying at least one quantifiable indicator of each of the diet-responsive conditions and measuring the at least one indicator for each of the patient during a four week baseline period; and monitoring each of the patients during the baseline period to determine a baseline quality of life. The plurality of patient are divided randomly between a first group and a second group. The diet program is administered to each of the patients in the first group during a ten week intervention period and each of the patient in the second group is maintained on a control diet with known beneficial effects on the at least one diet-responsive condition during the intervention period. The at least one indicator of each of the conditions is monitored for each of the patient after the intervention period.


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