Addison, ILNCT07428889Now EnrollingIRB Ready

Healthy Adult Clinical Trial in Addison, IL

Access cutting-edge healthy adult treatment through this clinical trial at a research site in Addison. Study-provided care at no cost to qualified participants.

Sponsored by Shaklee Corporation

Quick Self-Assessment

See if you qualify for this Addison location

Preparing your pre-screening questions…

Expert Care in Addison

Access healthy adult specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related healthy adult treatment provided free

Apply for This Addison Location

Check if you qualify for this healthy adult clinical trial in Addison, IL

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Addison

    Convenient for IL residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Addison site if eligible
  4. 4Begin participation

About This Healthy Adult Study in Addison

The objective of this study is to evaluate nicotinamide adenine dinucleotide (NAD+) in response to a proprietary nutritional supplement in generally healthy adults, compared to placebo.

Sponsor: Shaklee Corporation

Who Can Participate

Inclusion Criteria

Males and females, ≥45 to ≤65 years of age
BMI ≥18.5 and \<30.0 kg/m2
Ambulatory and currently free of injury or other physical impairment that hinders mobility.
Willing to use personal smart phone with operating system (Android version 12.0 or newer; iOS version 16 or newer).
Willingness to maintain current skin care regimen and avoid any skin-related medical procedures.
Willing to adhere to all study procedures, including lifestyle considerations and sign forms providing informed consent to participate in the study and authorization to release relevant protected health information to the Clinical Investigator.

Exclusion Criteria

Is currently following, or planning to be on, a weight loss regimen.
Weight loss or gain \>4.5 kg.
History of gastrointestinal surgery for weight reducing purposes.
History of an eating disorder (e.g., anorexia nervosa or bulimia nervosa, binge eating) at the discretion of the Clinical Investigator.
History of neurologic disorder that could produce cognitive deterioration.
History of bouts of delirium, confusion, repeated minor head injury or a single injury.
History of unconventional sleep patterns or a diagnosed sleep disorder.
History of any infective or inflammatory brain disease.
Use of tobacco/nicotine products.
Use of hemp/marijuana products.
Unstable use of any prescription medication.
Unstable use (initiation or change in dose) of hormonal contraceptives or therapy.
Use of any dietary supplements (orally or infused), other than a conventional once daily multi-vitamin.
Use of medication(s) or dietary supplement(s) known to affect absorption.
Recent history of or strong potential for alcohol or substance abuse.
Exposed to any non-registered drug product.
A score of \<7 on the Vein Access Scale Assessment.
History or presence, on the basis of the medical history or screening labs, of clinically important cardiac, renal, hepatic, endocrine (including diabetes mellitus), pulmonary, gastrointestinal, biliary, pancreatic, or neurological disorders.
Uncontrolled hypertension.
Known allergy to any ingredients contained in the study product.
Any signs or symptoms of active infection of clinical relevance.
History or presence of cancer in the prior 2 years, except for non-melanoma skin cancer.
History of any major trauma or major surgical event.
Female who is pregnant, planning to be pregnant during the study period, lactating, or is of childbearing potential with unstable use of sex hormones for contraception.
An employee or representative who has a financial interest in Sponsor organization.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Addison?

Yes, this clinical trial (NCT07428889) has an active research site in Addison, IL that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Healthy Adult Treatment Options in Addison, IL

If you're searching for healthy adult treatment options in Addison, IL, this clinical trial (NCT07428889) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Addison research site is actively enrolling participants for this clinical trial. You'll receive care from experienced healthy adult specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all healthy adult clinical trials near you to find additional studies recruiting in your area.

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