Grant Details
| Grant Number: |
1R21CA292185-01 Interpret this number |
| Primary Investigator: |
O'Cleirigh, Conall |
| Organization: |
Massachusetts General Hospital |
| Project Title: |
Adapting and Testing a Smoking Cessation Intervention for Transgender and Gender-Diverse Individuals |
| Fiscal Year: |
2024 |
Abstract
Despite the substantial decrease in smoking prevalence over the past 50 years, persistent and significant
disparities in tobacco use remain among clinical and non-clinical populations of adults who smoke. Cigarette use
among clinical populations, including patients with HIV and those with significant developmental stress, ranges
from approximately 40–70%, compared with 10–12% among non-clinical populations.1 Clinical populations with
HIV and developmental stressors also show dramatically higher rates of e-cigarette use relative to non-clinical
populations (26.5% vs. 5.5% in some samples of adults who smoke).2,3 Adults managing HIV and developmental
stressors may be particularly vulnerable to the consequences of tobacco use through increased heart disease
risk, and smoking may hinder recovery from HIV and other related illnesses.4 Differential responses to
developmental stressors, the stress of managing HIV and its treatment, and co-occurring clinical concerns such
as anxiety and depression further contribute to these differences in tobacco use. Anxiety and depression are
major impediments to smoking cessation5-7 and are more prevalent among people with developmental stress
and people living with HIV than in non-clinical samples. Anxiety symptoms co-occur with smoking at high rates
and significantly impair cessation success.8,9 Similarly, depressed mood and major depressive disorder—both
more common among people who smoke than among those who do not10-12—are associated with reduced odds
of cessation.13 The high prevalence of anxiety and depression among clinical populations of adults who smoke
therefore leaves these individuals particularly vulnerable to cessation difficulties. A tailored smoking cessation
intervention that builds cognitive-behavioral skills for cessation while also reducing stress and associated anxiety
and depression symptoms has strong potential to mitigate tobacco use.
We propose to adapt an existing smoking cessation intervention, QUIT,14 to address the unique needs of adults
with developmental stress who smoke. In focus groups with individuals who use tobacco (N ≤ 32) and providers
(N ≤ 8), we will explore the ways in which stress and associated anxiety/depression compromise cessation, and
identify content in the current version of QUIT that does and does not meet participants’ needs. Providers will
also comment on anticipated implementation barriers. Following the ADAPT-ITT model, these qualitative data
will inform adaptation of the intervention. We will then test the feasibility and acceptability of the adapted
intervention (QUIT 2.0) in a pilot randomized controlled trial (RCT; N = 60), assessing for signals of clinically
meaningful change in biologically verified 7-day point-prevalence abstinence, average number of cigarettes
smoked, and stress, anxiety, depression, and distress tolerance. If QUIT 2.0 is feasible and acceptable, it will be
ready for a hybrid efficacy/effectiveness trial. We will also include a non-randomized, retrospective comparison
group—matched on age, sex, and average number of cigarettes smoked per day in the past week—consisting
of adults with HIV who completed the original, un-adapted intervention (QUIT 1.0).
Publications
Identifying the ways in which tobacco cessation interventions have been tailored for sexual and gender minority individuals: A systematic review.
Authors: Fogarty J.J.
, Fertig M.R.
, Gulbicki L.
, Ashar D.
, O'Cleirigh C.
, Stanton A.M.
.
Source: Journal Of Health Psychology, 2024-10-04 00:00:00.0; , p. 13591053241284083.
EPub date: 2024-10-04 00:00:00.0.
PMID: 39364831
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