Financial Incentives for Homeless Smokers: A Community-based RCT

Sponsor
Massachusetts General Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04445662
Collaborator
National Cancer Institute (NCI) (NIH), National Institutes of Health (NIH) (NIH)
400
1
2
32.7
12.2

Study Details

Study Description

Brief Summary

This community-based randomized controlled trial will test the effect of contingent financial rewards on smoking abstinence among homeless-experienced adult cigarette smokers.

Participants will be recruited from 3 Boston Health Care for the Homeless Program locations:

a shelter clinic, a day center clinic, and a medical center clinic. All participants will be offered a varenicline prescription and tobacco coaching. Incentive arm participants will receive escalating financial rewards for saliva cotinine levels <30 ng/ml, assessed 10 times over 12 weeks. Embedded qualitative interviews will explore the mechanisms of on-treatment and post-treatment effects of financial incentives on smoking abstinence in the context of homelessness.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

People experiencing homelessness have a 3.5-fold higher prevalence of cigarette smoking in comparison to non-homeless people, contributing to 2-fold higher rates of lung cancer and 3- to 5-fold higher rates of tobacco-attributable death. Homeless smokers want to quit, but studies have not yet uncovered the optimal approach to help them do so. In an 8-week pilot randomized controlled trial (RCT) at Boston Health Care for the Homeless Program (BHCHP), we found that financial incentives for smoking abstinence were associated with 7-fold higher odds of brief smoking abstinence in comparison to a non-incentivized control condition. These results suggest that financial incentives are a promising approach for reducing smoking in this vulnerable population, but further investigation in a larger sample is needed to improve the duration of on-treatment abstinence, assess post-treatment effects, and better understand mechanisms of action and contextual factors that may influence treatment response.

To address the above gaps in evidence, we will conduct a community-based RCT of financial incentives for smoking abstinence among adult smokers at BHCHP. Recognized as a leader in homeless health care, BHCHP serves 12,000 currently and formerly homeless patients annually throughout greater Boston. We will randomize 400 participants recruited from 3 BHCHP sites: a shelter clinic, a day center clinic, and a medical center clinic. All participants will be offered 12 weeks of varenicline, 5 sessions of tobacco coaching, and 10 cotinine monitoring visits over a 12-week period. Participants randomized to the financial incentives arm (n=200) will receive escalating debit card payments (range $25-$70) at each monitoring visit for saliva cotinine levels <30 ng/ml. Control arm participants (n=200) will receive a fixed payment ($10) at each monitoring visit regardless of their saliva cotinine level. We will use an embedded-experiment mixed methods design, where qualitative ('qual') data collection is embedded within a larger quantitative ('QUAN') RCT with the following specific aims:

Aim 1. (QUAN) To determine the effect of the financial incentives intervention on cotinine-verified 7-day smoking abstinence at A) the end of treatment (12 weeks) and B) 12 weeks after treatment (24 weeks).

Hypotheses: Incentive arm participants will have significantly greater cotinine-verified 7-day smoking abstinence than control arm participants at A) 12 weeks and B) 24 weeks.

Aim 2. (qual) To assess why, how, and under what circumstances homeless smokers A) achieve abstinence in response to financial incentives and B) maintain abstinence after incentives are stopped.

Interviews with participants at A) 12 weeks (N=30) and B) 24 weeks (N=20) will examine cognitive ('why?'), procedural ('how?'), and contextual ('under what circumstances?') dimensions of their response to financial incentives to generate hypotheses about potential mechanisms for on-treatment and post-treatment effects and to inform modifications of the intervention for future use.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
400 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Financial Incentives for Homeless Smokers: A Community-based RCT
Actual Study Start Date :
Jun 10, 2021
Anticipated Primary Completion Date :
Sep 1, 2023
Anticipated Study Completion Date :
Mar 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Control (n=200)

Varenicline Tobacco coaching Saliva cotinine monitoring with fixed payments ($10) regardless of results

Drug: Varenicline
Day 1 - 3: 0.5 mg daily Day 4 - 7: 0.5 mg twice daily Day 8 - Week 12: 1 mg twice daily Dose/schedule may be adjusted based on medical history and clinician judgement
Other Names:
  • Chantix
  • Behavioral: Tobacco coaching
    5 one-on-one tobacco cessation coaching sessions over 12 weeks
    Other Names:
  • Smoking cessation counseling
  • Experimental: Financial incentives (n=200)

    Varenicline Tobacco coaching Saliva cotinine monitoring with escalating payments ($25-70) for levels <30 ng/ml

    Behavioral: Financial incentives
    Escalating financial rewards for saliva cotinine levels <30 ng/mL, assessed 10 times over 12 weeks
    Other Names:
  • Contingency management
  • Drug: Varenicline
    Day 1 - 3: 0.5 mg daily Day 4 - 7: 0.5 mg twice daily Day 8 - Week 12: 1 mg twice daily Dose/schedule may be adjusted based on medical history and clinician judgement
    Other Names:
  • Chantix
  • Behavioral: Tobacco coaching
    5 one-on-one tobacco cessation coaching sessions over 12 weeks
    Other Names:
  • Smoking cessation counseling
  • Outcome Measures

    Primary Outcome Measures

    1. Cotinine-verified 7-day smoking abstinence at 12 weeks [12 weeks]

      Point-prevalent smoking abstinence, defined as self-report of not smoking in the past 7 days and verified by a salivary cotinine level <10 ng/ml.

    Secondary Outcome Measures

    1. Cotinine-verified 7-day smoking abstinence at 24 weeks [24 weeks]

      Point-prevalent smoking abstinence, defined as self-report of not smoking in the past 7 days and verified by a salivary cotinine level <10 ng/ml.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age ≥18 years old

    • Lifetime smoker of ≥100 cigarettes with current daily smoking of ≥5 cigarettes per day, verified by a saliva cotinine level of ≥30 ng/mL

    • Ready to try quitting smoking within the next 3 months

    • Proficient in English

    • Currently or formerly homeless

    • Have a primary care provider within BHCHP system

    Exclusion Criteria:
    • Unable to provide informed consent

    • History of allergic reaction to varenicline

    • Currently pregnant, planning to become pregnant, or breastfeeding

    • Past-month suicidal ideation with plan or intent, or past 12-month history of suicidal behaviors or attempts

    • Psychiatric hospitalization in the past 3 months

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Boston Health Care for the Homeless Program Boston Massachusetts United States 02118

    Sponsors and Collaborators

    • Massachusetts General Hospital
    • National Cancer Institute (NCI)
    • National Institutes of Health (NIH)

    Investigators

    • Principal Investigator: Travis Baggett, MD, Massachusetts General Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Travis Paul Baggett, Assistant Professor of Medicine, Massachusetts General Hospital
    ClinicalTrials.gov Identifier:
    NCT04445662
    Other Study ID Numbers:
    • 2019P000034
    • R01CA235617-01
    First Posted:
    Jun 24, 2020
    Last Update Posted:
    Mar 4, 2022
    Last Verified:
    Mar 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by Travis Paul Baggett, Assistant Professor of Medicine, Massachusetts General Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 4, 2022