HIV Infections, Smoking, Smoking Cessation
Conditions
Keywords
Botswana, Smoking cessation, BAPS, Counseling, HIV
Brief summary
The main purpose of this research study is to compare traditional behavioral smoking cessation therapy with a different type of behavioral therapy-known as behavioral activation problem solving (BAPS)-for smoking cessation. Standard smoking cessation counseling (SC) focuses on self-monitoring, identifying smoking triggers and how to manage them, relaxation and social support for non-smoking, and relapse prevention. BAPS focuses on recognizing he feelings you are having that lead to smoking and how to overcome those feelings and focus on activities that discourage you from smoking and avoid activities that encourage you to smoke. Both counseling types include gathering information about your personal smoking patterns, your likes, dislikes, and other personal characteristics about your lifestyle. Half of participants who enroll in the study will receive standard smoking cessation counseling (SC) and half will receive BAPS counseling. We will compare the rates of quitting smoking across the two groups at the end of treatment (study week 10), and 12 weeks after the end of treatment (study week 26)
Detailed description
Eligible patients will be randomized to one of the treatment arms, which will involve 5 phone-delivered counseling sessions over a 9-week treatment phase. While enrolled in this research study, you will also be asked not to use any smoking cessation treatment (including medication or behavioral therapy) other than that which is provided to you within the context of this clinical study. The session will either be run by a study coordinator or a counselor. The study coordinator gathers information about you so we can understand whether or not the program is working. The study coordinator will be the person conducting the assessments. The counselor works with you to help you stop smoking. Study visits are described in more detail below. Intake * Complete the study informed consent with a research staff member. You will have the opportunity to have your questions answered before signing the study consent form. If you chose not to sign this form, no procedures will be performed * Complete a breath carbon monoxide (CO) assessment to measure your smoke exposure. Carbon monoxide is a poisonous gas that comprises less than 1% of the air we breathe and is also produced through smoking a cigarette. Your CO levels provide an indication of how much cigarette smoke you have been exposed to. * Complete paper and pencil assessments of your demographics, alcohol and smoking history, smoking and health behaviors, and mood. Weeks 1,3,5,7, and 9 * Phone-delivered counseling session (SC or BAPS) that will last between 30-60 min to help prepare you for your upcoming quit attempt (Week 2, Target Quit Day) * These sessions will focus on reinforcing your success and reviewing your quit plan or on reestablishing another quit date and restarting the smoking cessation process Weeks 10 and 26 * Assessments only, the same ones administered during the intake session * If you are quit (have not smoked in the past 7 days), you will be asked to come in to provide a CO breath sample
Interventions
BEHAVIORALCessation Counseling
Two different types of smoking cessation counseling
Sponsors
Abramson Cancer Center at Penn Medicine
National Institute on Drug Abuse (NIDA)
University of Botswana
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
We will use permuted block randomization with random block sizes between 6 and 9 and stratified by sex and depressive symptoms. The blocks will ensure near 1:1 balance throughout the study. The random block sizes will protect against selection bias by preventing staff from predicting which intervention any one individual will be assigned. We will stratify by sex to ensure balance of women in both arms since smoking is more common in men. We will stratify by depressive symptoms to ensure balance in testing whether the effect of BAPS is differential between those with and without greater degrees of distress. While a Mood Module of PRIME-MD score of \>5 symptoms is commonly used as a threshold for depression (Spitzer et al., 1994), we are also targeting lower level symptoms with this intervention having found that lower levels are associated with health behaviors such as medication adherence (Gross et al., 2017).
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* \>18 years old * Smoking cigarettes daily for the past 30 days * HIV+ with HIV viral load of \<1000 copies/mL, obtained within the 6 months prior to enrollment * Receiving HIV care at Infectious Diseases Care Clinics (IDCCs) in and around Gaborone * Able to communicate in English OR Setswana and provide written informed consent * Planning on residing in the geographic area for at least the next 7 months
Exclusion criteria
* Cognitive deficits that impair their ability to provide informed consent * Current untreated and unstable diagnosis of alcohol dependence (if past use and stable for \>30 days, eligible) * Psychosis * Use of chewing tobacco, snuff or snus * Recent , current, or planned use (next 7 months) of nicotine substitutes or smoking cessation treatments
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Smoking Cessation | At week 26, EOT | be 7-day point prevalence abstinence at week 26 (24-weeks post-TQD; self-reported abstinence for 7 days prior to the assessment and breath CO ≤8 ppm) |
Countries
Botswana
Outcome results
None listed