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Effect of Revival Soy on Weight Loss and Skin, Hair, and Nails in Premenopausal Women

Primary Purpose

Skin Aging, Weight Loss

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Revival Soy Dietary Supplement
Sponsored by
Physicians Pharmaceuticals, Inc.
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Skin Aging focused on measuring Soy, Dermatology, Skin, Hair, Finger Nails, Weight Loss, Body Mass Index, Photoaging of Skin, Skin Wrinkling

Eligibility Criteria

25 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Females Age: 25-45 years. BMI between 30 - 40 kg/m2. Motivated to lose weight. Subjects must be in general good health as determined from a medical history. Subjects must have mild to moderate photoaging. Subjects must use a shampoo from the approved list without change for the entire duration of the study. Must not be consuming soy supplements or other soy products currently. Must not be pregnant (negative pregnancy test at screening) and agree not to become pregnant during the course of the study. Subjects must read and sign the informed consent form after the nature of the study has been fully explained. Exclusion Criteria: Subjects with known allergies or sensitivities to ingredients contained in the dietary supplement. Subjects who are required to spend excessive time in the sun (i.e. lifeguards, other outdoor workers). Subjects who are currently participating or have participated within the last 4 weeks in any other clinical study (i.e., dermal patch, use tests, investigational drug or devices, etc.). Subjects viewed by the investigator as not being able to complete the study. Subjects who are unwilling to leave all of their current skin care products unchanged for the 6 months of the study. Subjects who are unwilling to leave all of their current nail care products unchanged for the 6 months of the study. Subjects who are unwilling to leave all of their current oral medications unchanged for the 6 months of the study. Subjects who have experienced large variations in body weight during the previous 3 months Subjects currently using other weight loss medications or supplements. Subjects who had surgical intervention for the treatment of obesity.

Sites / Locations

  • Dermatology Consulting Services

Outcomes

Primary Outcome Measures

Investigator assessed appearance of skin (roughness, wrinkling, dyspigmentation, and redness) at baseline and after 3 and 6 months
Investigator assessed appearance of hair (roughness, dullness, lack of manageability, and scalp flaking) at baseline and after 3 and 6 months
Investigator assessed appearance of finger nails (roughness, ridging, flaking, and splitting) at baseline and after 3 and 6 months.

Secondary Outcome Measures

Body weight at monthly intervals
Body mass index (BMI) at the baseline and study completion
Subject-perceived changes in appearance of skin, hair, and finger nails at baseline and after 3 and 6 months

Full Information

First Posted
July 13, 2006
Last Updated
July 20, 2009
Sponsor
Physicians Pharmaceuticals, Inc.
Collaborators
Dermatology Consulting Services, High Point NC
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1. Study Identification

Unique Protocol Identification Number
NCT00352157
Brief Title
Effect of Revival Soy on Weight Loss and Skin, Hair, and Nails in Premenopausal Women
Official Title
Effect of Revival Soy on Weight Loss and Appearance of Skin, Hair, and Nails in High BMI Premenopausal Women
Study Type
Interventional

2. Study Status

Record Verification Date
July 2009
Overall Recruitment Status
Completed
Study Start Date
July 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
March 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Physicians Pharmaceuticals, Inc.
Collaborators
Dermatology Consulting Services, High Point NC

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine if dietary consumption of Revival Soy can improve the appearance of the skin, hair, and finger nails and support weight loss in overweight, premenopausal women.
Detailed Description
The researchers hypothesize that supplementation of Revival® Soy products to overweight premenopausal women as part of a soy-based meal replacement diet plan will: Improve the health and appearance of the skin by normalizing skin pigmentation and reducing wrinkles, Improve the health and appearance of hair by enhancing sheen and ease of combing, and Improve the health and appearance of nails by enhancing shine, flexibility, and strength. Stimulate a loss in weight and a reduction in the Body Mass Index (BMI), For this study, obese (BMI = 30-40 kg/m2) premenopausal women (25-45 years of age) with mild to moderate photoaging (n=40) will receive either a Revival® soy shake (20 grams soy protein with 160 mg total isoflavones; n=20) or a placebo shake (20 grams of milk protein with 0 mg isoflavones; n=20) daily for 6 months. The subjects will be asked to come into the office for a total of seven visits, at baseline and at monthly intervals for 6 months. At baseline, month 3, and month 6, the subjects will be asked to complete a questionnaire in order to provide self-reported improvements related to hair, skin, and nail health. Following completion of the questionnaire, the investigator and the dermatology clinic staff will examine the subjects to assess the health and appearance of their skin, hair, and nails at baseline, month 3, and month 6. After acceptance into the study, a registered dietitian will instruct the study subjects in the use of a low-energy (1,200 - 1,500 kcal/day) diet that incorporates 2 soy-based daily meal replacements (shakes, ~500 kcal), a minimum of 5 daily servings of fruits and vegetables (~300 kcal), and one entrée (~400 - 500 kcal). Subjects will be required to keep a dietary food intake record of all food and supplement use during the trial. Anthropometric data (height, body weight, waist circumference and hip circumference) will be collected at baseline and at monthly intervals.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Skin Aging, Weight Loss
Keywords
Soy, Dermatology, Skin, Hair, Finger Nails, Weight Loss, Body Mass Index, Photoaging of Skin, Skin Wrinkling

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Single
Allocation
Randomized
Enrollment
40 (false)

8. Arms, Groups, and Interventions

Intervention Type
Behavioral
Intervention Name(s)
Revival Soy Dietary Supplement
Primary Outcome Measure Information:
Title
Investigator assessed appearance of skin (roughness, wrinkling, dyspigmentation, and redness) at baseline and after 3 and 6 months
Title
Investigator assessed appearance of hair (roughness, dullness, lack of manageability, and scalp flaking) at baseline and after 3 and 6 months
Title
Investigator assessed appearance of finger nails (roughness, ridging, flaking, and splitting) at baseline and after 3 and 6 months.
Secondary Outcome Measure Information:
Title
Body weight at monthly intervals
Title
Body mass index (BMI) at the baseline and study completion
Title
Subject-perceived changes in appearance of skin, hair, and finger nails at baseline and after 3 and 6 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Females Age: 25-45 years. BMI between 30 - 40 kg/m2. Motivated to lose weight. Subjects must be in general good health as determined from a medical history. Subjects must have mild to moderate photoaging. Subjects must use a shampoo from the approved list without change for the entire duration of the study. Must not be consuming soy supplements or other soy products currently. Must not be pregnant (negative pregnancy test at screening) and agree not to become pregnant during the course of the study. Subjects must read and sign the informed consent form after the nature of the study has been fully explained. Exclusion Criteria: Subjects with known allergies or sensitivities to ingredients contained in the dietary supplement. Subjects who are required to spend excessive time in the sun (i.e. lifeguards, other outdoor workers). Subjects who are currently participating or have participated within the last 4 weeks in any other clinical study (i.e., dermal patch, use tests, investigational drug or devices, etc.). Subjects viewed by the investigator as not being able to complete the study. Subjects who are unwilling to leave all of their current skin care products unchanged for the 6 months of the study. Subjects who are unwilling to leave all of their current nail care products unchanged for the 6 months of the study. Subjects who are unwilling to leave all of their current oral medications unchanged for the 6 months of the study. Subjects who have experienced large variations in body weight during the previous 3 months Subjects currently using other weight loss medications or supplements. Subjects who had surgical intervention for the treatment of obesity.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zoe D Draelos, M.D.
Organizational Affiliation
Dermatology Consulting Services, High Point NC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dermatology Consulting Services
City
High Point
State/Province
North Carolina
ZIP/Postal Code
27262
Country
United States

12. IPD Sharing Statement

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Effect of Revival Soy on Weight Loss and Skin, Hair, and Nails in Premenopausal Women

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