Supplement Study: Strength, Testosterone, Sexual Function, Quality of Life

STUDY PARTICIPANT RECRUITMENT:

Subjects will be recruited via mass advertising in the Charlotte Metropolitan area. Healthy subjects will be screened during recruitment to determine study eligibility (via email and phone). The Charlotte metropolitan area is the largest in the Carolinas, and the sixth largest metropolitan area in the Southeastern region of the United States. Male participants 40 to 70 years of age will be selected who match the listed inclusion and exclusion criteria (next page). The planned distribution of participants by racial/ethnic groups will reflect the demographics of the metropolitan area [White non-Hispanic (60%), Black non-Hispanic (24%), Hispanic (10%), and Asian or Pacific Islander non-Hispanic (3.5%)]. Those subjects who meet all of the inclusion criteria and none of the exclusion criteria will be enrolled and randomized into the study. The study duration for each subject will be 6 weeks. There will be a total of 3 visits for this study. Following recruitment, there will be a 2-week washout period for PDE5 medications. At each of the three morning visits (7:00-9:00 am), subjects will fill in the symptom log (retrospective 3-week period) and have their blood drawn to analyze serum levels of free and total testosterone, and to be tested for strength (isometric hand grip, leg/lower back, YMCA bench press) and body composition (8-point bioelectrical impedance). All subjects will be required to fast overnight for at least 9 hours prior to each visit. Subjects will also be required to abstain from all vigorous exercise and sexual activity at least 24-hours prior to each visit. Within three days prior to each lab visit, subjects will use Survey Monkey via the Internet to fill in responses to three questionnaires: CSFQ, WHO-QOL, and POMS.

RESEARCH PLAN A. V1 - Baseline Visit - Week 0 Prior to the first lab visit, subjects will be recruited according to the listed inclusion and exclusion criteria. Subjects who agree to participate in the study, will be sent the Informed Consent Document (ICD) for review and signature. Subjects will fill in the Medical Health Questionnaire (MHQ) via Survey Monkey to obtain demographic, lifestyle, and medical histories. Following recruitment, there will be a 2-week washout period for PDE5 medications. Within three days prior to the first lab visit, subjects will supply responses to the CSFQ, WHO-QOL, and POMS Questionnaires via Survey Monkey. The compensation contract will be reviewed and signed.

• Informed Consent: At the first lab visit (V1), all subjects will review the Informed Consent Document (ICD) that was previously sent via email attachment, and receive a signed copy.
• Questionnaires: Responses to the CSFQ, WHO-QOL, and POMS questionnaires sent prior to the first lab visit via Survey Monkey will be reviewed for completeness. Subjects will fill in the symptom log.
• Blood Sample: Subjects will have their blood drawn for analysis of free and total testosterone. Subjects will be asked to come in to the clinic during the early morning having fasted for at least 9 hours prior to the visit and refrained from having sexual intercourse 24 hours prior to the visit.
• Anthropometric and Strength Measures: Subjects will be measured for height and weight, and percent body fat using 8-point BIA. Handgrip and leg/lower back strength will be assessed with dynamometers (Figure 3). Subjects will also be tested for upper body strength using the YMCA bench press test (reps with 80-pound barbell set with a metronome for 30 lifts per minute).
• Randomization and Study Product Dispensing: Subjects will be assigned a randomization number, and receive a 3 week supply of the study product. The study product will be contained in supplement trays with specific dates and instructions applied. Subjects must return the supplement trays at the next two lab visits to verify compliance with the dosing regimen.

B. V2 -Mid-Study Visit (Week 3)

• Retrieval Procedures: Subjects will return their supplement tray and any unused study product.
• Intercurrent Medical History and Concomitant Medication History: Subjects will be interviewed by the clinic staff to determine whether there have been any changes in their medical history, whether they have started taking any new medications.
• Questionnaires: Responses to the CSFQ, WHO-QOL, and POMS questionnaires sent within 3-days prior to the second visit via Survey Monkey will be reviewed for completeness. Subjects will fill in the symptom log (3 week retrospective).
• Blood Sample: Subjects will have their blood drawn for analysis of free and total testosterone. Subjects will be asked to come in to the clinic during the early morning having fasted for at least 9 hours prior to the visit and refrained from having sexual intercourse and all exercise 24 hours prior to the visit.
• Anthropometric and Strength Measures: Subjects will be measured for weight, and percent body fat using 8-point BIA. Handgrip and leg/lower back strength will be assessed with dynamometers, and upper body strength with the YMCA bench press test.
• Study Product Dispensing: Subjects will receive their final 3-week supply of the study supplements. Subjects must return the supplement tray at the final lab visit to verify compliance with the dosing regimen.

C. V3 -End-of-Study Visit (Week 6)

• Retrieval Procedures: Subjects will return their supplement tray and any unused study product.
• Intercurrent Medical History and Concomitant Medication History: Subjects will be interviewed by the clinic staff to determine whether there have been any changes in their medical history, whether they have started taking any new medications.
• Questionnaires: Responses to the CSFQ, WHO-QOL, and POMS questionnaires sent within 3 days prior to the final lab visit via Survey Monkey will be reviewed for completeness. The final symptom log will be completed. The compensation contract will be reviewed.
• Blood Sample: Subjects will have their blood drawn for analysis of free and total testosterone. Subjects will be asked to come in to the clinic during the early morning having fasted for at least 9 hours prior to the visit and refrained from having sexual intercourse 24 hours prior to the visit.
• Anthropometric and Strength Measures: Subjects will be measured for height and weight, and percent body fat using 8-point BIA. Handgrip and leg/lower back strength will be assessed with dynamometers, and upper body strength with the YMCA bench press test.

D. Investigational Study Products Formula 1 - a Men's Perfect Multi Formula boosted by extra Magnesium and key vitamins and co-factors. 4 tablets.

Formula 2 - an Herbal blend - we're naming "AndroVitality" with Rhaponticum, Rhododendron caucasicum, 180 mg magnesium, 10 zinc and 2000 IU vitamin D. 4 tablets.

INSTRUCTIONS: Take 4 capsules daily, with water on an empty stomach. If the study participant reports that they get an upset stomach from ingesting the capsules, they will be allowed to consume a small snack. The investigators will store the study product in a locked cabinet in a limited access room, in accordance with the manufacturer's instructions, i.e. in a dry place and at room temperature. Purity Products will provide the ASU-NCRC Human Performance Lab with sufficient study product to complete this study. The supplements and placebo product, will be supplied to the Primary Investigator (DCN) in boxes using A, B, and C codes so that both the investigators and the subjects will be blinded regarding the type of supplement being ingested. Supplement trays will be given to each subject, and will contain labels with the following information:

• Study code number
• Patient number
• Directions of use
• Storage instructions

E. Concomitant Medication Prohibited Medications and Interventions

The following products and interventions are not permitted while the subject is in this study:

• No erectile dysfunction medications or dietary supplements containing ingredients advertised for influences on sexual function or testosterone.

F. Data Analysis and Statistical Methods Data will be entered into an Excel worksheet under the direction of the Primary Investigator (DCN) and the Research Manager. Data statistical analysis (with identifier information deleted) will be conducted by Drs. Nieman, Canu, and Broman-Fulks. The basic statistical model will be a 3 (group) x 3 (time) repeated measures ANOVA within the SPSS Generalized Linear Model (GLM). Subjects will be randomized in equal numbers to one of three groups: two supplement groups; Placebo. The blinding code will be created by Purity Products and stored in a locked cabinet, and provided to the Primary Investigator AFTER all data have been collected. The file linking ID numbers and names of study participants will be stored at uStor, the secure storage site for Appalachian State University (http://ustorcloud.appstate.edu). Analysis and interpretation of data from the CSFQ, WHO-QOL, and POMS questionnaires will be under the direction of clinical psychologists Drs. Canu and Broman-Fulks. Prior to the initiation of the study, this protocol including the informed consent form will be submitted to the ASU IRB and the trial will not start until unconditional approval is received. All guidelines from the ASU IRB for protection of personal data will be followed. The Primary Investigator will assign a subject number to each subject that will be used for identification whenever subject related data are recorded for the sponsor or reported. Subjects who are randomized, but drop out prior to completing the study will be recorded. A record of reasons why subjects drop out of the study will be maintained. After data analysis the Primary Investigator will summarize the results in a final report which accurately reflects the clinical data of this study.