Raleigh, NCNCT06072547Now EnrollingIRB Ready

Cigarette Smoking Behavior Clinical Trial in Raleigh, NC

Access cutting-edge cigarette smoking behavior treatment through this clinical trial at a research site in Raleigh. Study-provided care at no cost to qualified participants.

Sponsored by Altria Client Services LLC

Quick Self-Assessment

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Expert Care in Raleigh

Access cigarette smoking behavior specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related cigarette smoking behavior treatment provided free

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Check if you qualify for this cigarette smoking behavior clinical trial in Raleigh, NC

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

Why Participate?

  • No-Cost Study Care

  • Local to Raleigh

    Convenient for NC 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 Raleigh site if eligible
  4. 4Begin participation

About This Cigarette Smoking Behavior Study in Raleigh

The goal of this clinical trial is to learn about the role of flavored on!® nicotine pouch products (the research products), an oral tobacco-leaf-free product, in the replacement of cigarettes with the use of the research products among adults who smoke cigarettes. The main question it aims to answer is whether flavored (vs. non-flavored) research products generate greater reduction of cigarette smoking among adults who smoke cigarettes. Participants will be provided with research products to use for 6 weeks. Researchers will compare the reduction in cigarette smoking between participants with access to a complete flavor profile of research products and participants with access to only the Original (non-flavored) variety of research product to see if reduction in cigarette smoking is greater among those with access to flavored research products.

Sponsor: Altria Client Services LLC

Who Can Participate

Inclusion Criteria

Has signed the Informed Consent Form (ICF) and is able to read and understand the information provided in the ICF.
Healthy adults who smoke cigarettes and are 22 to 65 years of age (inclusive) at screening.
Smokes an average of at least 5 cigarettes per day for the last 12 months.
Does not intend to use an FDA-approved treatment for nicotine dependence within the next 60 days (as assessed at screening).
Interested in replacing combustible cigarettes with a smoke-free tobacco product.
Willing and able to comply with the requirements of the study.
Owns a smart phone with text message and data capabilities compatible with necessary surveys.

Exclusion Criteria

Participant enrollment numbers met (in sub-group or entire study).
Participant, or their first-degree relative (e.g., parent, sibling, child, spouse) or household member, is a current or former employee of the tobacco or e-vapor industry.
Participant, or their first-degree relative (e.g., parent, sibling, child, spouse) or household member is a named party or class representative in litigation involving a tobacco or e-vapor company.
Participant, or their first-degree relative (e.g., parent, sibling, child, spouse), or household member, is a current or former employee of a marketing consultant, market research firm, advertising or promotions agency, television or radio station, magazine or newspaper, government regulatory agency or public policy advocacy group, or law firm or legal department of a company.
Participant self-reports being "in poor health."
Participants of childbearing potential (CBP) who have a positive pregnancy test (as assessed at screening) or are nursing or planning to become pregnant during their participation.
Participant has an allergy/sensitivity to menthol or menthol-containing products or phenylalanine.
Participant has any other self-reported health restrictions.
Participant self-reports cardiovascular disease, cancer, diabetes, or is being treated for high blood pressure.
Participant self-reports periodontal disease, gum disease or bleeding, open mouth sores or ulcers.
Participant self-reports as wanting to stop using tobacco products in the next 60 days.
Participant has participated in one tobacco research study in the past 30 days OR a tobacco research study lasting two weeks or longer in the past 90 days.
Participant is unable to read, speak or understand English.
Participants who ever used at least a pack of nicotine pouch products or currently uses nicotine pouch products.
Participant who smokes marijuana more than once a week.
Heterosexually active participants of CBP (not sterilized by tubal ligation, oophorectomy, hysterectomy, or other surgical methods, or post-menopausal) that do not agree to practice medically appropriate methods of birth control (or remain abstinent) during the course of the trial and for 30 days after the last use of the research product. Medically acceptable methods of birth control include: vasectomy, vaginal diaphragm with spermicide, intrauterine device, hormonal birth control (oral, injected, patch, or implanted), condom with spermicide, or sponge with spermicide.
Taking psychoactive medications (e.g., antipsychotics or mood stabilizers).
Cannot participate in the study for any reason (e.g., medical, psychiatric, and or social reason) as judged by the Investigator or designated medical staff based on all available information from the screening period.

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 Raleigh?

Yes, this clinical trial (NCT06072547) has an active research site in Raleigh, NC 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.

Cigarette Smoking Behavior Treatment Options in Raleigh, NC

If you're searching for cigarette smoking behavior treatment options in Raleigh, NC, this clinical trial (NCT06072547) 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 Raleigh research site is actively enrolling participants for this clinical trial. You'll receive care from experienced cigarette smoking behavior 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 cigarette smoking behavior clinical trials near you to find additional studies recruiting in your area.

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