RECRUITING

Perceptions of E-Cigarettes and Synthetic Cooling Agents, The ICE Study

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study evaluates how synthetic cooling additives like WS-3 and WS-23 impact e-cigarette perceptions, use behavior, and toxicant exposure.

Official Title

The ICE Study: Perceptions of E-Cigarettes and Synthetic Cooling Agents (R01)

Quick Facts

Study Start:2024-05-08
Study Completion:2028-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06208202

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:21 Years to 29 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Aged 21-29 years
  2. * Current exclusive e-cigarette (EC) user (defined as ≥ weekly use over the past 3 months)
  3. * Willing to provide informed consent and abstain from using their EC at least 12 hours prior to the four lab sessions
  4. * Read and speak English
  1. * Recently COVID-19+ (defined as positive test in the past 30 days) or a recent COVID-19 hospitalization (defined as a hospitalization within the past 6 months)
  2. * Unstable or significant psychiatric conditions (past and stable conditions will be allowed)
  3. * History of cardiac event or distress within the past 3 months
  4. * Are currently pregnant, planning to become pregnant, or breastfeeding (will be verified with urine pregnancy test)
  5. * Have suffered from any serious lung disease or infection (e.g. , tuberculosis, cystic fibrosis, or lung cancer) in the past 30 days
  6. * Have hemophilia or another type of bleeding disorder
  7. * Are blind, severely visually impaired, deaf, hard of hearing, or have a severe motor disability

Contacts and Locations

Study Contact

The Ohio State Comprehensive Cancer Center
CONTACT
800-293-5066
OSUCCCClinicaltrials@osumc.edu

Principal Investigator

Alayna P Tackett, PhD
PRINCIPAL_INVESTIGATOR
Ohio State University Comprehensive Cancer Center

Study Locations (Sites)

Ohio State University Comprehensive Cancer Center
Columbus, Ohio, 43210
United States

Collaborators and Investigators

Sponsor: Ohio State University Comprehensive Cancer Center

  • Alayna P Tackett, PhD, PRINCIPAL_INVESTIGATOR, Ohio State University Comprehensive Cancer Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-05-08
Study Completion Date2028-06

Study Record Updates

Study Start Date2024-05-08
Study Completion Date2028-06

Terms related to this study

Additional Relevant MeSH Terms

  • Abuse Tobacco
  • Exposure