RECRUITING

Integrating Financial Coaching and Smoking Cessation Coaching

Conditions

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 conduct a two-arm, parallel-group randomized controlled trial. The study will recruit and randomize 900 smokers (n=450 per arm) to either: (1) Control: Standard Smoking Cessation Counseling or (2) Intervention: Integrated Financial-Smoking Cessation Counseling.

Official Title

Integrating Financial Coaching and Smoking Cessation Coaching for People With Low Income Who Smoke: a Randomized Controlled Trial

Quick Facts

Study Start:2022-12-08
Study Completion:2027-12-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05154669

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 to 100 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * age ≥18 years,
  2. * smokes ≥5 cigarettes per day,
  3. * interested in receiving smoking and financial counseling,
  4. * self-reported income below 200% of the current federal poverty level,
  5. * New York City resident,
  6. * speaks English or Spanish language (the interventions and measures have not been validated in other languages),
  7. * able to provide informed consent, and
  8. * does not have a representative who manages his/her funds.
  9. * people who know a current past study participant (to avoid intervention contamination)
  10. * People who have a medical contraindication to using nicotine replacement therapy:
  11. * allergy to nicotine patch
  12. * pregnancy or intention to become pregnant over the next 12 months
  13. * breastfeeding
  14. * heart attack in the past 2 months
  15. * underlying arrhythmia
  16. * ongoing or worsening angina.
  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

Erin Rogers, DrPH
CONTACT
646-501-2544
erin.rogers@nyulangone.org

Principal Investigator

Erin Rogers, DrPH
PRINCIPAL_INVESTIGATOR
NYU Langone Health

Study Locations (Sites)

NYU Langone Health
New York, New York, 10016
United States

Collaborators and Investigators

Sponsor: NYU Langone Health

  • Erin Rogers, DrPH, PRINCIPAL_INVESTIGATOR, NYU Langone Health

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 Date2022-12-08
Study Completion Date2027-12-01

Study Record Updates

Study Start Date2022-12-08
Study Completion Date2027-12-01

Terms related to this study

Additional Relevant MeSH Terms

  • Smoking