This Phase II RCT is examining the efficacy of a 5-session positive affect intervention that is designed to boost and extend the effectiveness of CM with HIV-positive, methamphetamine-using MSM (
www.clinicaltrials.gov; NCT01926184). All enrolled participants are referred to a community-based, 12-week CM program that must be initiated prior to randomization. CM visits are completed at the San Francisco AIDS Foundation and all other trial-related activities occur at a separate field site in the community. Screening and enrollment are anticipated to continue through June of 2017 and follow-up assessments will be completed in September of 2018. All relevant procedures are approved by the Institutional Review Boards for the University of California, San Francisco and Northwestern University, and this RCT received a certificate of confidentiality from the National Institute on Drug Abuse. The data safety and monitoring plan is overseen by the University of California, Los Angeles Data Safety and Monitoring Board for Addiction Medicine, which holds annual meetings to review participant-related events and overall progress for this RCT.
Recruitment, screening, and enrollment for the RCT
HIV-positive, methamphetamine-using MSM are recruited for this RCT through three primary sources. First, men initiating services at a community-based CM program complete a brief consent form to be contacted by study staff to learn more about the RCT. Second, direct recruitment is conducted using flyers and palm cards that are distributed in HIV medical clinics, AIDS service organizations, bars and clubs, bath houses, and via social media. Third, an incentivized snowball sampling method is employed where eligible participants receive a maximum of $30 for referring up to three individuals who are subsequently judged to be eligible for the RCT.
To be eligible for this RCT, participants must meet the following inclusion criteria: 1) 18 years of age or older; 2) identify as a MSM; 3) provide documentation of HIV-positive serostatus (i.e., letter of diagnosis or ART medications other than Truvada that are matched to their photo identification); and 4) provide a urine or hair sample that is reactive for methamphetamine metabolites. All potentially eligible participants referred from the community-based CM program are scheduled for an in-person screening visit. Participants recruited from other sources are required to report methamphetamine use in the past 30 days to be eligible for an in-person screening visit.
At the in-person screening visit, participants complete a signed informed consent, consent for specimen banking, a detailed tracking form with at least one secondary contact, and a consent to search relevant death registries. Participants also complete a Health Insurance Portability and Accountability Act (HIPAA) release to access treatment records at the CM program. Those who provide a urine sample that is reactive for methamphetamine or have documented evidence of a reactive urine screen for methamphetamine from the CM program are immediately scheduled for a baseline assessment. Those without evidence or recent methamphetamine use from urine screening provide a hair sample for toxicology testing. Hair is collected from the occipital region of the scalp where possible, but it is also collected from other sites (i.e., beard, body) where necessary to obtain biological confirmation of recent methamphetamine use. After the screening visit, participants receive a $50 pre-loaded debit card. Participants are excluded after the screening visit for the following reasons: 1) prescription of a psychostimulant (e.g., Adderall) that cross reacts with urine screening for methamphetamine; 2) inability to provide informed consent; 3) unable to follow the study protocol; and 4) judged by the principal investigators that it is not in the best interests of the individual to participate.
This RCT is being conducted in partnership with a community-based, 12-week CM program for methamphetamine-using MSM that is operated by the San Francisco AIDS Foundation. Individuals who are interested in the CM program complete a detailed intake that includes assessments of the frequency with which they use methamphetamine and engage in sexual behaviors with men. MSM who report using methamphetamine at least weekly on average in the past three months provide a urine sample for toxicology screening at the intake visit and are enrolled in the CM program irrespective of urine toxicology results.
All clients in the CM program are encouraged to pursue abstinence from methamphetamine and other stimulants during the 12-week CM period. Urine sample collection is directly observed by CM program staff. The voucher for the initial sample that is negative for methamphetamine and cocaine metabolites is worth $2.00. Vouchers increase in value by 25 cents for each consecutive stimulant-free sample to a maximum of $10.00. Participants earn an $8.50 bonus voucher for every third consecutive stimulant-free sample. A rapid reset procedure allows participants to return to their place in the escalating reinforcement schedule after producing three consecutive urine samples that are non-reactive for methamphetamine and cocaine [
19]. The total possible reinforcement is $330, and participants may choose to receive incentives earned any time during or after the 12-week CM intervention period.
Concurrent with the CM urine screening visits, clients may participate in a drop-in group that provides social support for continuing to pursue goals for stimulant use reduction or abstinence. Drop-in groups also provide opportunities to facilitate linkage to community-based services including formal substance abuse treatment and HIV care. After completing the 12 weeks of urine screening visits, individuals are invited to attend aftercare sessions to continue to forge social networks that are supportive of avoiding stimulant use and develop relapse prevention plans. Those who complete the 12-week CM program with aftercare are invited to continue attending regular drop-in groups to provide support and mentorship to men who are actively completing the thrice weekly urine screening visits.
Positive affect intervention
Affect regulation treatment to enhance methamphetamine intervention success (ARTEMIS) is a multi-component, individually-delivered 5-session intervention targeting positive affect regulation. This intervention was adapted from prior clinical research testing the feasibility and acceptability of a positive affect intervention for recently diagnosed HIV-positive persons [
37]. The extant positive affect intervention protocol was adapted and pilot tested in a RCT with 21 methamphetamine-using MSM receiving CM [
36]. Based on the results of the pilot RCT, the positive affect intervention protocol was further refined prior to initiating the present Phase II RCT with HIV-positive, methamphetamine-using MSM.
The original positive affect intervention protocol consists of eight skills:
(1) positive event noting; (2) positive event capitalizing; (3) gratitude; (4) informal and formal mindfulness; (5) positive reappraisal; (6) personal strengths; (7) attainable goals; and (8) acts of kindness. As shown in Table
1, we modified the original protocol to tailor this positive affect intervention for HIV-positive, methamphetamine-using MSM. These adaptations included additional content to optimize delivery of the core positive affect regulation skills with this population and new components designed to facilitate greater engagement in the recovery process (e.g., problem-focused coping, values clarification, and referral to community-based services). Informed by prior research examining the efficacy of mindfulness-based relapse prevention [
38‐
40], participants also complete meditation exercises during ARTEMIS intervention sessions to further enhance metacognitive awareness and assist individuals in coping more effectively with methamphetamine withdrawal. Self-report measures of stimulant craving before and after each session as well as a measure of positive and negative affect before sessions one, three, and five are completed by participants. Participants can choose to receive $20 in cash per session or two $50 debit cards upon completion of all five sessions, complete detailed home practice exercises, receive a workbook with each of the skills outlined and an iPod shuffle that is pre-loaded with meditation exercises to facilitate regular practice.
Table 1
Positive affect intervention protocol for HIV-positive, methamphetamine-using MSM
1 | Noticing Positive Events | Psychoeducation on Stimulant Withdrawal |
Capitalizing on Positive Events | Capitalizing on Non-Reactive Urine Toxicology |
Gratitude | Breathing Retraining with Positive Event Imagery |
2 | Mindfulness (Informal and Formal) | Breath Meditation |
Self-Compassion |
3 | Positive Reappraisal | Problem-Focused Coping & Reasoned Action |
Breath Meditation |
4 | Strengths | Values Clarification |
Attainable Goals | Mountain Meditation |
5 | Altruism | Volunteer opportunities |
Linkage to More Intensive Community-Based Services |
Loving Kindness Meditation |
Session one begins with an overview of the intervention and psychoeducation about the stressful nature of stimulant withdrawal that individuals experience during CM. Positive affect regulation skills are framed as one way of more effectively coping during this stressful period. Participants are encouraged to start by noticing positive events that occur in daily life and explore ways to amplify or extend the experience of positive emotions related to these events (i.e., capitalizing). In addition to identifying positive events in their daily lives, participants are asked to describe positive emotions that stem from having a urine screen during CM that was non-reactive for stimulants (where applicable) and continue to capitalize on this positive event. The concept of gratitude as a feeling of appreciation or thankfulness that can stem from positive events is also introduced. Finally, facilitators deliver a modified breathing retraining exercise that includes positive event imagery to assist participants with capitalizing on a positive event in vivo. For home practice, participants are asked to complete the “One Good Thing” exercise where they note a positive event that happened each day and briefly describe responses to the event. Participants are also asked to begin keeping a gratitude journal that continues throughout the 5-session intervention [
41].
Session two includes mindfulness-based skills training to cultivate non-judgmental, present-centered awareness. By facilitating metacognitive awareness, mindfulness promotes greater insight into cognitive and emotional responses to events which may reduce craving and decrease the likelihood that individuals engage in the overlearned response of substance use [
39]. Informal mindfulness exercises are completed in-session to encourage individuals to develop an enhanced awareness of daily experiences (e.g., brushing one’s teeth). Participants also complete a brief formal mindfulness-based meditation practice (i.e., breath awareness) and receive an iPod shuffle preloaded with three meditation exercises: breath awareness, mountain meditation and loving kindness meditation [
42]. Finally, this session concludes with a discussion of the importance of self-compassion as a way of coping with stressful life circumstances. Participants are encouraged to be more tolerant of their imperfections by developing a supportive and caring self-orientation. Home practice includes informal mindfulness practice (i.e., “Practicing Being Present in Daily Life” exercise), formal mindfulness meditation using the iPod shuffle, and the gratitude journal. Participants may listen to any of the three recordings on the iPod shuffle.
Session three focuses on executing effective coping responses. Participants are introduced to the concept of positive reappraisal whereby individuals change their interpretations of stressful events to support successful adaptation. The facilitator reviews ways in which changing thoughts about a stressful event (i.e., positive reappraisals) can affect emotional responses and subsequent behaviors. This is generally consistent with the approach of cognitive-behavioral treatments like the Matrix Model [
43], but there is no requirement that the initial appraisal of an event is distorted. Especially where aspects of a stressful event are uncontrollable, participants are encouraged to examine ways in which the experience could have been worse or how they learned something new as a result of enduring this stressful event (both examples of positive reappraisals). Participants are asked to identify a recent stressful event and work with the facilitator to practice different methods for positive reappraisal in session.
Another important component of session three is reviewing methods of enhancing coping effectiveness in response to controllable situations [
44,
45]. Where aspects of stressful circumstances are controllable, participants are encouraged to explore problem-focused coping strategies that can be implemented to reduce the experience of stress. Participants briefly review possible problem-focused coping strategies with the facilitator. This process of executing effective coping responses by engaging in positive reappraisal and then problem-focused coping is presented as “reasoned action” where managing emotional responses to an event is a critical first step towards addressing any aspects that are within one’s control. Participants also complete a formal mindfulness-based meditation practice (i.e., breath awareness) at this session. Home practice includes daily positive reappraisal exercises where participants identify stressful events, develop positive reappraisal(s), and delineate concrete actions that can be taken to address the identified ‘problem.’ Participants also continue with the meditation practice and the gratitude journal.
Session four begins with an exercise where participants are asked to reflect on personal strengths. This process promotes greater insight into personal sources of resilience and enhances self-affirmation, which has been linked to enhanced problem solving and self regulation [
46,
47]. After identifying personal strengths, participants are asked to examine the degree to which these strengths are linked to personal values or the ways in which strengths assist one with living values in action. Then, participants are introduced to the concept of attainable goals, which are presented as short-term goals that are
Achievable, have
Clear steps, and a definitive
Endpoint (ACE). Strengths and values are presented as important resources that energize goal-oriented progress. Participants are encouraged to examine ways in which leveraging personal strengths could facilitate progress toward attainable goals. Values are framed as the underlying meaning structures that remind individuals why attainable goals are important. This session concludes with the mountain meditation which focuses on embracing personal strengths and resilience in the midst of stress [
42]. For home practice, participants are asked to monitor progress towards completing attainable goals identified in session while noting personal strengths that assist with progress toward these goals. Participants also continue with the meditation practice and the gratitude journal.
Session five targets altruism by discussing findings that small acts of kindness may enhance psychological adjustment and bolster physical health [
48,
49]. Participants review ways in which they can incorporate small acts of kindness into their daily activities and review formal volunteer opportunities available in the community. Participants also complete the loving kindness meditation [
42], which focuses on experiencing feelings of love and caring toward another person. The facilitator also leads the participant through a thorough skills review of all the positive affect and coping skills delivered throughout the five sessions. This portion of the intervention focuses on discussing positive aspects of the ARTEMIS sessions for the participant and ways in which he can continue to pursue treatment in the community. Tailored referrals are provided to assist participants with engaging in more intensive mental health or substance abuse treatment.
Staff training and fidelity monitoring
Each staff member receives a detailed training on assessment protocols for this RCT: 1) privacy and confidentiality including HIPAA security practices and human subjects protection training; 2) obtaining informed consent; 3) blood borne pathogens training 4) safe shipping of biological specimens training 5) laboratory safety for researchers training 6) technology training including use of laptops for data collection and the participant database; 7) interviewing techniques such as building rapport, working with diverse populations, cultural sensitivity, population-specific issues and referrals, maintaining confidentiality, basic quantitative and qualitative interview skills; 8) a detailed suicidality assessment protocol; and 9) and role playing of assessments or individual sessions.
Intervention facilitators are provided with a detailed manual that describes the procedures for administering the five individual intervention sessions. Facilitators conducted mock sessions and the audio recordings of these sessions are reviewed by a clinical supervisor who then meets one-on-one with the facilitator to provide feedback on delivery of intervention content and process-oriented techniques. Mock sessions are repeated until the facilitator is judged to be competent with each of the five intervention sessions.
The protocol for monitoring the fidelity of the positive affect intervention sessions during the course of the study includes audio recording of sessions for weekly review with a clinical supervisor and fidelity checklist ratings that are reviewed monthly in group supervision. Audio recordings of intervention sessions are reviewed by the fidelity monitor and the clinical supervisor to assess adherence to the protocol, delivery, interpersonal skills, rapport, and session flow. Approximately 10 % of all positive affect intervention sessions are coded using fidelity rating checklists with detailed feedback provided to facilitators.
Follow-up assessments and specimen banking
At 3, 6, 12 and 15 months after enrollment in CM, each participant completes computer-based follow-up assessments that are administered by a trained interviewer who has not administered intervention or attention-control sessions to that participant. Self-reported substance use and sexual behavior measures are completed by participants using audio computer-assisted self-interviewing to enhance reliability and validity [
51]. Urine samples for on-site toxicology testing for recent use of methamphetamine, cocaine, opiates, marijuana, and benzodiazepines (Redwood Biotech iCup®; Santa Rosa, CA) are collected at each assessment. Peripheral venous blood samples are collected at baseline as well as 6, 12, and 15 months following enrollment in CM to measure HIV viral load and CD4+ T-cell count. Participants receive a pre-loaded $50 debit card for completing each of the assessment visits over the 15-month period.
Participants are also asked to provide an additional 25 ml of peripheral venous blood using two 10 mL EDTA and two 5 mL PAXgene® tubes (Qiagen, Inc.) at baseline as well as 6, 12, and 15 months following enrollment in CM. Using EDTA tubes, leukocyte DNA is extracted and banked. Approximately three mL of plasma are also banked. PaXgene® tubes are used for isolation and stabilization of RNA. These tubes are progressively frozen and banked.
Outcome analyses
We will first generate one-way frequency tables for all variables and measures of central tendency and variability for continuous variables (e.g., means, medians, standard deviations) to perform range checks, quantify the amount of missing data, and yield valuable descriptive findings. Chi-square tests, t-tests, and comparable two-group non-parametric tests will be used to investigate equality of potential confounders (e.g., homelessness) across the intervention and attention-control conditions at baseline. Similarly, we will confirm that there are no differences in the mean number of intervention and attention-control sessions completed as well as no differential attrition by study arm.
Based on our extensive experience working with this population, we anticipate a maximum of 20% attrition over the 15-month investigation period. Attrition analyses will compare respondents who complete all measurements to those who do not based on baseline characteristics and we will test for differential attrition by intervention condition. Direct maximum likelihood and multiple imputation will be used to address incomplete data because these methods make the relatively mild assumption that missing data arise from a conditionally missing-at-random process [
60].
Intent-to-treat analyses will be conducted primarily using multilevel random coefficient models (i.e., hierarchical linear modeling; HLM). These models incorporate random intercepts and slopes for each participant based on the participant’s multiple measurements over time [
61]. Initial models will be unadjusted and compare outcome trajectories for participants in ARTEMIS + CM and Attention-Control + CM across time via the group-by-time interaction effect. If preliminary analyses detect imbalance in potential confounders across the groups that cannot be satisfactorily addressed via covariate adjustment, we will substitute causal inference methods based on the Rubin causal model (e.g., propensity score weighting; marginal structural models) to obtain population-level effects of the intervention under the assumption of balanced confounders between the two groups [
62‐
66]. A priori planned comparisons will be performed to test group differences at 3, 6, 12, and 15 months for both the primary and secondary outcomes. These planned comparisons will be evaluated at α = .05; any subsequent post-hoc comparisons will be adjusted via simulation-based stepdown methods to maintain a nominal Type I error rate of .05 [
67].
The primary outcome will be log10 HIV viral load over the 15-month follow-up. Sustained HIV viral suppression will be examined as a secondary outcome using logistic regression of the binary outcome of sustained virologic suppression over the 15-month follow-up (0 = no; 1 = yes) on randomization group assignment. Other continuous secondary outcomes that will be examined in intent-to-treat analyses include: CD4+ T-cell count, positive and negative affect, stimulant craving, and self-reported stimulant use. Ordered categorical and categorical outcomes assessed repeatedly over the 15-month follow-up include: ART adherence and persistence, a positive urine toxicology result for stimulants, potentially amplified transmission risk partners stratified by methamphetamine use, and any potentially amplified transmission risk.