RECRUITING

Smoking Cessation Program in the Construction Sector

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

The main objective of this study is to identify the optimal adaptive smoking cessation program for the construction sector in terms of effectiveness, cost-effectiveness, and potential implementation.

Official Title

Expanding the Role of the Safety Manager to Implement a Workplace Smoking Cessation Program in the Construction Sector

Quick Facts

Study Start:2024-04-10
Study Completion:2027-02-28
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06098144

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:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * ≥ 18 years
  2. * Involved in decision making
  3. * Willing to participate in the implementation development and evaluation
  4. * ≥ 18 years
  5. * Be a safety manager
  6. * No plans to leave the company within the next year
  7. * Bilingual
  8. * Willing to receive training in smoking cessation treatment
  9. * Willing to deliver the smoking cessation treatment to workers
  10. * Be a construction worker
  11. * ≥ 18 years
  12. * Have smoked on average 5 or more cigarettes daily for the past year
  13. * Willing to make a serious quit attempt in the next 30 days
  14. * Planning to stay in the company for the next 6 months
  15. * Own a telephone and plan to keep it active for the next 12 months
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Taghrid Asfar, MD
CONTACT
305-243-3826
tasfar@miami.edu
Alejandra Casas, BS
CONTACT
305-243-0362
axc623@miami.edu

Principal Investigator

Taghrid Asfar, MD
PRINCIPAL_INVESTIGATOR
tasfar@miami.edu

Study Locations (Sites)

Don Soffer Clinical Research Center
Miami, Florida, 33136
United States

Collaborators and Investigators

Sponsor: University of Miami

  • Taghrid Asfar, MD, PRINCIPAL_INVESTIGATOR, tasfar@miami.edu

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 Date2024-04-10
Study Completion Date2027-02-28

Study Record Updates

Study Start Date2024-04-10
Study Completion Date2027-02-28

Terms related to this study

Additional Relevant MeSH Terms

  • Smoking Cessation
  • Tobacco Use Cessation
  • Tobacco Smoking