RECRUITING

Clinical Research Evaluating Smoking Cessation With E-Cigarettes and Nicotine Therapy

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Conditions

Smoking CessationObesity and Obesity-related Medical Conditionsobesityelectronic cigarettesharm reduction

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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 project will investigate the effects of alternative nicotine products on smoking, weight gain, and related outcomes.

Official Title

Clinical Research Evaluating Smoking Cessation With E-Cigarettes and Nicotine Therapy

Quick Facts

Study Start:2025-04-01
Study Completion:2027-08-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06948058

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * body mass index (BMI) ≥ 30 kg/m2 (i.e., obese)
  2. * smoked ≥ 5 cigarettes/day during the past year
  3. * 21 or older (due to minimum legal age EC restrictions)
  4. * exhaled breath carbon monoxide (CO) level \> 6 ppm at Baseline (BL) (to confirm self-reported smoking)
  5. * willing to use EC or NRT for 8 weeks
  6. * access to a Bluetooth-enabled smartphone/tablet (to permit remote measurement of CO and other outcome variables)
  1. * received smoking cessation treatment of any kind in the past 30 days (actively quitting smoking),
  2. * currently using EC or NRT more than 2 days/week (this may affect responses to study-supplied products)
  3. * hospitalized for mental illness in past 30 days
  4. * heart-related event (e.g., heart attack, severe angina) in past 30 days
  5. * residing with another person currently enrolled in the study
  6. * pregnant, nursing, or planning to become pregnant in the next 6 months
  7. * medical contraindication for study or product use (e.g., allergy to adhesives)
  8. * taken prescription weight loss medication in the last 30 days

Contacts and Locations

Study Contact

CRESCENT Study Research Staff
CONTACT
401-203-5339
CRESCENT@brown.edu

Study Locations (Sites)

Brown University
Providence, Rhode Island, 02912
United States

Collaborators and Investigators

Sponsor: Brown University

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 Date2025-04-01
Study Completion Date2027-08-31

Study Record Updates

Study Start Date2025-04-01
Study Completion Date2027-08-31

Terms related to this study

Keywords Provided by Researchers

  • obesity
  • electronic cigarettes
  • harm reduction

Additional Relevant MeSH Terms

  • Smoking Cessation
  • Obesity and Obesity-related Medical Conditions