Abstract
Purpose of Review
The objective of this scoping review was to examine the range of published evidence on recruitment approaches and outcomes of US adolescents and young adults (AYA) ages (18–29 years) into human immunodeficiency virus (HIV)–related behavioral research studies during the past 10 years.
Recent Findings
Implementation of effective behavioral research strategies among HIV at-risk and infected AYA is key to ending the HIV epidemic and necessitates successful recruitment strategies.
Summary
A comprehensive search was executed across four electronic databases. Of the 1697 identified studies, seven met inclusion criteria with six of these seven directed to HIV prevention. Most studies used online recruitment as part of a hybrid strategy, and combined field-based/in-person and online methods. Recruitment strategies and outcomes, resources and compensation, procedures for consent, and timelines varied among all seven studies. Our results highlight the need for development of recruitment models in alignment with behavioral strategies aimed to treat and prevent HIV among US AYA.
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Introduction
Presently there are 1.2 million human immunodeficiency virus (HIV)–infected individuals 13 years and older living in the US. Blacks/African Americans and Hispanics/Latinos represent 65% of all HIV infections, and young people ranging from 13 to 34 years of age make up 23% of the US HIV prevalence [1]. At year-end in 2018, the largest percentage of undiagnosed HIV infection was among persons aged 13–24 years (44.9%), followed by persons aged 25–34 years (29.3%) [2]. Between 2014 and 2018, HIV infection rates increased among persons aged 13–24 years [2]. Across all age cohorts, the primary risk factors for HIV acquisition are behavioral: male-to-male sex (66%), and female (16%) and male (4%) heterosexual contact [2]. Survey data from the Youth Risk Behavior Survey (YRBS) collected from 2005 to 2015 indicate that approximately half of all US high school students reported ever having sexual intercourse [3]. As such, trajectories of HIV risk begins with early sexual debut in adolescence and continue through adulthood, lending to behavioral interventions for HIV prevention [4,5,6].
The United States (U.S.) Department of Health and Human Services (HHS) initiated, Ending the HIV Epidemic in 2019, a strategic plan with the goal of a 90% reduction in new HIV cases by 2030 [7]. The pillars of this national initiative are HIV prevention, diagnosis, treatment, and outbreak response among high-risk and vulnerable cohorts [7]. A compendium of evidence-based strategies directed to HIV prevention, diagnosis, and treatment for HIV at-risk and infected individuals includes 194 studies, spanning the past 14 years (2005–2019) [8]. Of these 194 interventions, a total of 51 studies included Black and African American, Hispanic, and Latino adolescents and young adults (AYA), ages 13–24 years of age, categorized as follows: HIV prevention (41 studies), HIV diagnosis (one study), HIV treatment (eight studies), or outbreak response (one study), (Appendix 1). Ending the HIV Epidemic is contingent upon using robust scientific data and evidence to develop effective strategies, resources, and programs targeting HIV-infected and at-risk cohorts; identification of best practices for reaching and recruiting these cohorts into such programs is also urgently needed [7, 9•].
Participant recruitment, or the activities conducted across the lifespan of a research protocol, leading to enrollment or accrual [10] is a critical component of research success [11]. Recruitment challenges are described as a primary cause for premature termination of clinical trials [12, 13]. Yet to date, there is a paucity of evidence summarizing approaches and strategies for successful research recruitment of high-risk and vulnerable populations.
Blacks/African Americans and Hispanics/Latinos are underrepresented in HIV research trials; face long-standing barriers to research participation, deeply rooted in social norms and culture [14, 15] and experience participant mistrust and biases by research staff [16]. Recruitment of AYA into HIV-related research studies pose additional challenges, such as individual and community-levels barriers operationalized as follows: insufficient understanding of research, self-presentation bias, issues of parental consent, access to clinical research, mistrust, and stigma [17]. These recruitment barriers and gaps result in significant delay to the advancement of HIV-related behavioral research strategies for prevention, diagnosis, treatment, and outbreak response among Black/African American and Hispanic/Latino AYA.
Recruitment of participants is typically the responsibility of individual investigators at academic research institutions. However, investigators may not have the resources and/or experience to achieve participant accrual targets [10]. Moreover, published behavioral studies infrequently detail investigator initiated recruitment procedures, strategies, and or outcomes of these approaches [11] including related advantages or disadvantages. To the best of our knowledge, there have been no published literature reviews detailing recruitment methods of US AYA ages (18–29 years) into HIV-related behavioral research studies. Hence, the primary objective of this scoping review is to examine the range and extent of published evidence on recruitment approaches and outcomes of US AYA ages (18–29 years) into HIV-related behavioral research studies during the past 10 years. A secondary objective is to summarize advantages and disadvantages of these recruitment approaches and identify gaps in the available published evidence base with recommendations for research and practice.
Methods
This review was guided by the methodological framework for scoping reviews outlined by Arksey and O’Malley (2005) and Preferred Reporting Items for Systematic Review and Meta-Analyses (PRISMA) guidelines [18]. A scoping review is conducted to rapidly identify key concepts underpinning a research area and relevant gaps [19]. Five stages have been proposed for conducting a scoping review: (1) identifying the research question, (2) identifying relevant studies, (3) study selection, (4) charting the data, and (5) collating and summarizing [19].
Stage 1. Research Question
For the purposes of this present scoping review, our research question is, “What is known from the published evidence base on the recruitment of US AYA ages (18-29 years) into HIV-related behavioral research studies?” Consistent with the methodological framework of a scoping review, our approach was broad to minimize the potential of missing relevant citations [19]. We did however need to set parameters and three primary operational definitions to help manage the volume of evidence and identify relevant studies.
Adolescence/Young Adulthood
Our rationale for study inclusion criterion of 18–29 year olds was due to increased HIV risk and rates of new infection in this cohort [2]. This age range (late teens to late twenties) is characterized as emerging adulthood, a district developmental phase remarkable for growth and exploration of relationship and career choices, and worldviews [20]. The life course of emerging adulthood is culturally constructed and represented by challenges, complexity, and opportunity [20], making it a prime time for HIV prevention and or risk reduction with behavioral interventions and programs.
HIV-Related Behavioral Research
We defined HIV-related behavioral research as intervention studies directed to HIV prevention (i.e., HIV testing) or treatment (medication adherence) of HIV-infected or HIV at-risk AYA.
Recruitment was operationalized to broadly include activities conducted in a research protocol leading to participant enrollment in a research study, such as time, effort, expertise, and availability of the research team; resources afforded to the recruiter; and the availability of infrastructure, tools, and data to rationally optimize recruitment activities as they are conducted [10, 21].
Stage 2. Identifying Relevant Studies
A health sciences librarian assisted in the development and performance of the literature search. Four bibliographic databases, PubMed, CINAHL, PsycINFO, and Web of Science, were systematically searched for studies focused on recruitment methods for engaging HIV-positive and at-risk emerging young adults in research. The final literature searches were carried out between March 10th and March 31st 2020.
Search Strategy
General search terms were selected a priori and revised based on preliminary findings. Examples of selected terms included HIV, recruitment, and clinical trials as topics, limiting to age groups corresponding with young adults. These terms were further defined so that “recruitment,” for example, was enhanced with synonyms such as enroll, participate, or “willingness to participate.” Standard medical subject heading terms (“MeSH” or CINAHL subject terms, and PsycINFO descriptors) were used along with keywords, truncation, and categorical limits for age and publication dates for approximately the last 10 years (See Table 3 in Appendix 2 for a complete search strategy). As terms were tested and strategies revised, studies were downloaded into an Endnote database and migrated to the Covidence platform [22] for final de-duplication. Study authors then performed manual review of abstracts for inclusion and exclusion, and data extraction.
Stage 3. Study Selection
Title and abstract screening was conducted by a primary reviewer; studies meeting a broad list of inclusion criteria were coded as “yes” (HIV-infected or at-risk population, conducted in US, behavioral intervention, study population with mean age greater than 17 years and/or less than 30 years). A primary reviewer completed full text review and was assisted by one trained, graduate-level reviewer to independently evaluate potentially relevant studies for final inclusion or exclusion by applying the full set of a priori inclusion/exclusion criteria.
Studies were selected for full text review if published in English in the continental US and addressing recruitment methods of HIV-positive and at-risk emerging adults for behavioral research. As emerging adults are defined as individuals 18 to 29 years old, we included studies with total sample age stratification of ≥ 40% in this age range [20]. We excluded studies not focused on recruitment of HIV-infected or at-risk emerging adults for HIV behavioral research. Biomedical, pharmacological drug testing and/ or HIV vaccine trials were therefore also excluded.
Stage 4. Charting the Data
Charting for a scoping review entails a descriptive analytic method in which key and standard information is collected on all included studies using a data charting form; this process is analogous to data extraction for a systematic review [19]. We charted the following information in a shared folder document: author, publication year, geographic location of recruitment, study design, purpose, inclusion criteria, recruitment timeline, sample characteristics, primary results, and conclusions (Table 1); recruitment strategies, resources needed, compensation, consent process, response rate(s), timeline, advantages, and disadvantages of each recruitment approach (Table 2). Categories for these tables were iterative in development, and expanded and refined during the process of scholarly discussion and team meetings. Charting of this data was collected by one researcher and reviewed by a second for agreement. A quality appraisal was not conducted, as the objective of this scoping review was to examine range and extent of published evidence on recruitment approaches and outcomes of US AYA ages (18–29 years) into HIV-related behavioral research studies.
Results
Stage 5. Collation and Summary
Overview
Results of our search strategy are illustrated in Fig. 1 [18]. This search strategy yielded a total of 6766 citations; 1697 studies met criteria for full text review, and seven studies met full criteria for final inclusion. An overview of included studies is provided in Table 1.
Study Purpose
When categorizing studies as per the national HIV initiative to end the HIV epidemic (HIV prevention, diagnosis, treatment, and outbreak response), five recruited participants for HIV prevention [11, 23,24,25,26,27]. Rapid HIV testing [25] and antiretroviral (ARV) adherence support for HIV treatment regimens [28] represented additional study goals. None of these seven studies recruited as part of research directed to HIV outbreak response.
Study Design
Five of the seven studies were randomized clinical trials [11, 23,24,25, 27], and two described recruitment for cross-sectional studies [26, 28]. New York City was a geographic location for participant recruitment, either as an exclusive site [11, 26] or as part of a recruitment strategy for one or more sites [25, 27]. Other geographic recruitment locations were Chicago [23], Los Angeles [24], or exclusive to online social media sites [28].
Characteristics
In total, 4239 individuals were enrolled in HIV prevention or ARV studies. HIV-seropositive status was an inclusion criterion for one of the seven studies [28]. Other studies recruited HIV-seronegative participants [23,24,25, 27] or both HIV-negative and -positive participants. Three studies limited their samples to men who have sex with men and/or transgender women [11, 23, 26] and one study was limited to female participants only [27]. Recruitment results varied with race/ethnicity. Two studies reported majority Black/African American samples [25, 27], one reported a majority Hispanic/Latino sample [26], and three a majority White sample [11, 23, 28]. Researchers of one study did not report on race/ethnicity [24].
Methods of Participant Outreach
These varied across studies. A summary of recruitment methods and associated advantages and disadvantages is presented in Table 2. In total, six studies used venue-based sampling at specific locations from lesbian, gay, bisexual, and transgender (LGBT) community centers [23] and drop-in centers for homeless youth [24] to bars, clubs [11, 25, 26], and shopping venues [27]. Online recruitment ranged from email invitation [23] to advertising on specific websites such as Facebook, Twitter, Craigslist, and dating-specific websites [11, 25,26,27,28]. Common resources identified across studies were recruitment personnel and field staff. One study also employed HIV test counselors [23].
Two studies reported participant compensation [24, 27]. One study gave participants $20 for completing a baseline survey and $5 for attendance at each of four subsequent sessions [24]. If a participant attended all four sessions, they were given $15 and $30 for completion of a 3-month follow-up survey. Another study gave $5 for participants recruited in-person, nothing for online recruitment, and $100 for full study participation [27]. Across studies, the consent process was face-to-face [24, 26], online [23, 28], or both [11, 25, 27] depending on mode of recruitment.
Recruitment Timelines
Recruitment timelines ranged from 4-months for an online approach [28] to 3-years with a hybrid strategy combining both online and field-based methods [25]. Recruitment response rates for field-based venues ranged from 6% at house ball events to 59% when recruiting participants from bars [26]. One study examined the impact of race/ethnicity on recruitment and found no significant differences in field-based primary screening or Internet-based enrollment [23]. However racial and ethnic differences were observed with initial Internet-based screening; Black and Latino YMSM were less likely to complete online screening compared with White YMSM [23]. In terms of eligibility prescreening and attendance at the first study visit, there is evidence to provide support for recruitment of 18 -to 29 year olds and Black participants through social media, community information tables, and word of mouth referrals [25]. In order to determine if venue-based sampling (VBS) results in recruitment bias, one study compared weighted and unweighted prevalence estimates of HIV risk and seroprevalence in a sample of MSM [26]. Among 18- to 29-year-old participants, weighted HIV prevalence was higher than the unweighted response.
Advantages and Disadvantages
Overall, online and social media-based recruitment ranged from a response rate of 1% on Twitter to 86% on Facebook [28]. While online recruitment methods yielded higher response rates than field-based methods, advantages and disadvantages were identified for each. For field-based recruitment, the ability to target specific venues [11, 26] and develop rapport between research staff and potential participants [23,24,25,26] were seen as advantages. Disadvantages were associated with smaller sample sizes [23, 24] and increased recruitment costs and person-hours needed in the field [11, 25, 26]. Advantages of online recruitment were decreased to negligible recruitment costs and the ability to access difficult-to-reach populations [11, 25, 28]. Disadvantages were the inability to target recruitment as easily as venue-based sampling [11, 27], difficulty in building rapport with study participants [25], and costs associated with certain online applications [25].
Discussion
This scoping review is among the first to examine the extent and range of recruitment approaches and related outcomes of US AYA ages (18–29 years) into HIV-related behavioral research studies during the past decade. Our results highlight a body evidence that is largely in development, offering a starting point for initiation of recruitment guidelines tailored to age, sex, gender, race/ethnicity, context, and HIV risk(s) and status. We highlight important considerations for behavioral scientists planning recruitment strategies targeting US AYA ages (18–29 years). These include characteristics of participants recruited via online and field-based recruitment approaches, associated timelines, advantages, disadvantages, and resources needed for the implementation of each strategy.
Our comprehensive review of nearly 1700 unique studies resulted in seven studies that provided detailed information on recruitment practices. While these studies provide invaluable information about how AYA are recruited into HIV-related behavioral research projects, they include seven out of nearly 1700 published studies. Interestingly, only one of these seven studies described a recruitment approach exclusive to AYA with HIV-seropositive status as part of an antiretroviral treatment adherence intervention [28]; the other six studies included HIV-seronegative or mixed samples. This finding is not surprising given that few effective treatment interventions exist for Black/African American and Latino/Hispanic HIV + AYA [29]. Additionally, we did not identify studies directed to recruitment for outbreak response, an important pillar of controlling the HIV epidemic [30]. Sample sizes among the seven included studies are larger than what has been previously published with HIV-infected and at-risk AYA in HIV-related behavioral research. More commonly, behavioral interventions with this cohort are small pilots and or not powered sufficiently [29, 31,32,33].
Geographic locations of the studies included in this scoping review were Chicago, IL, New York, NY, New Jersey, Massachusetts, and Los Angeles, CA, despite the south having a disproportionately high number of new HIV cases. For example, Louisiana, Florida, and Georgia are the three hardest hit US states with over 20 HIV cases per 100,000 [34] but are not represented among these seven studies. Distinct geographic contextual factors and barriers may offer some explanation for this finding including stigma, poverty, racial and funding inequalities, and HIV provider perceptions [35].
Among contributions of this scoping review is the delineation of online, field based, and hybrid recruitment approaches to reach AYA participants. Five of the seven studies used a recruitment approach [11, 23, 25, 27, 28] with an online component. Each of these studies however used distinct implementation procedures, as there is no gold standard. Among online platforms used by researchers for recruitment in this review, four of the five studies included Facebook [11, 25, 27, 28] and this is consistent with national trends for frequent Facebook use [36, 37]. Other online platforms were Craigslist, Twitter, Instagram, LinkedIn, Tumblr, and dating sites such as Adam4Adam, Grindr, Growlr, Hornet, Scruff, Jack’d, daddyhunt.com, Gay.com, and Squirt.org. Although survey data shows YouTube to be the most widely visited online platform, with 91% usage among 18–29 year olds [37], YouTube was not part of these online recruitment strategies. The proliferation of technology has allowed for implementation of online recruitment approaches, supporting the advancement of HIV/AIDS research; these strategies capitalize on use of existing platforms well-known and frequently visited by potential participants [38]. However, to date, there is little guidance on how to best implement these approaches in HIV/AIDS research [38].
Disadvantages of online recruitment methods for HIV research are well-described and entail ethical challenges such as privacy and data storage issues, risk for misinformation, and need for validity protocols [39, 40•]. Despite these challenges, online recruitment is efficient, at least in terms of time. Among studies reviewed, relatively large samples were recruited during a short time period (i.e., a few months). Using exclusive field-based recruitment approaches, these sample sizes might have required years to achieve. Yet this shortened time frame for study recruitment also poses disadvantages, as it minimizes the impact of historical factors on the research question [41] but also may not allow for adaptations to recruitment criteria if samples accrue too rapidly.
An important consideration for researchers considering online recruitment approaches is related to procedures for obtaining informed consent, as consenting participants online offers additional challenges and complexities. The five studies using online recruitment strategies obtained participant informed consent with online study procedures [11, 23, 25, 27, 28]. Yet study authors did not describe any type of validation procedures or protocols. The informed consent process requires that research participants fully understand the risks and benefits of participation as well as their rights as research subjects. Assessing this without interpersonal interaction can be challenging, although many researchers have developed short quizzes that are included as part of the informed consent process [42]. As online research becomes more common, it is likely that researchers will develop novel methods to ensure that the online informed consent process is valid and participant comprehension adequate. In one study of predominantly Black and African American adults at risk for HIV and with an education level of high school or less, comprehension of obtaining online informed consent using a tablet kiosk was directly examined; researchers’ demonstrated acceptability and a high rate of comprehension [43].
Studies using a field-based or in-person recruitment approach, either exclusively or as part of a hybrid recruitment strategy [11, 23, 25, 27], reached out to participants in physical locations such as nightlife locations [11, 26], LGBT or singles events [25, 26], and community service organizations [23, 24, 26, 27]. This recruitment approach allows for exposure to the venues in which participants interact with each other, and these physical venues can provide essential contextual information related to the research question being studied. While more costly, field-based recruitment allows for targeting participants that meet specific criteria, as participant characteristics are likely to vary by venue [44]. For example, findings from the Parsons (2013) study directly comparing Internet and field-based approaches for recruitment of MSM at risk for HIV demonstrated that participants recruited in the field were more likely to be Black and African American MSM 30–39 years of age; characteristics of the Internet-based cohort were white and older MSM [11].
Other considerations for behavioral scientists planning a field-based/in-person recruitment approach is the potential for a longer recruitment timeline. Two of seven studies were exclusive to field-based/in-person recruitment [24, 26]. These timelines were longer (12–15 months) in comparison to the one study with an exclusive online recruitment approach (4 months) [28]. One advantage of a longer recruitment timeline is to allow for eligibility criteria to be adjusted in response to characteristics of the accruing sample. In the past, this time was necessary to allow for data entry, cleaning, and analysis; however, current research protocols using electronic or online data collection may be able to adjust eligibility criteria more rapidly.
In addition to recruitment timelines, we report recruitment resources used for the various approaches in this scoping review, both representing important components of research planning for grant applications, study protocols, and budgets. Compensation of research participants in HIV research has received increased attention recently [45, 46], and what are considered ethical standards in this area may ultimately reach a consensus. In this present review, compensation varied among the seven studies with incentives ranging from none [11, 23, 25, 26], to non-financial [28] and financial incentives [24, 27]. Among the two studies providing financial incentives, the dollar amount was $65 [24] and $100 dollars [27] for completing all study activities.
Of note, Research Match (https://www.researchmatch.org/) was not described as a resource among studies in this review. Additionally, although six of the seven studies were affiliated with an academic institution, institutional support such as consultation with Clinical Science Translation and Implementation (CTSI) or Clinical Translation Sciences Awards (CTSA) center was not reported. Given the availability of resources and pooled researcher expertise associated with these and other funded academic centers, initiatives directed to enhance greater investigator alliance, and generation of institutional recruitment policies and procedures is likely to enhance participant accrual [10].
Limitations
In addition to the small sample of included studies described above, this review has a number of other limitations. These were large studies, ranging from 200 to 3096 participants, and thus represent the types of study that receive substantial external funding and use sophisticated analytic methods. It is entirely possible that smaller studies, and even evaluations of service projects, employ different recruitment methods, or employ these methods in different ways, potentially revealing additional strengths and weaknesses of their recruitment strategies. These studies were also published prior to the outbreak of COVID-19, a pandemic with enormous impact on scientific research, essentially banning in-person contact with potential research subjects and shutting down many of the venues most commonly used to recruit HIV positive AYA into behavioral research studies.
Findings of this scoping review yielded valuable information on implementing online and field-based recruitment strategies among HIV-infected and at-risk AYA ages 18 - 29 years to HIV-related behavioral research studies, including the types of recruitment, venues in which recruitment takes place, and the advantages and disadvantages of these strategies. The majority of included studies used online recruitment as part of a hybrid strategy, and combined field-based/in-person and online methods. It should again be noted, however, that only seven studies meeting our inclusion criteria were ultimately identified. This reflects a contradiction that is also the reason for this review: recruitment strategies are a key component of behavioral HIV research but are rarely the focus of analysis and dissemination of study findings.
Ending the HIV epidemic by 2030 is a highly ambitious goal. An important step towards this goal is recruiting HIV-infected and at-risk AYA into the behavioral interventions and programs needed for HIV prevention, diagnosis, treatment, and outbreak response. While online recruitment and informed consent is a highly promising approach to increase reach and representation in HIV-related behavioral research studies, validation protocols and procedures are essential to ensure the ethical conduct of research with a vulnerable population. Behavioral scientists need to remain mindful that online recruitment approaches are not a replacement for field-based/in person strategies, as each has distinct advantages, limitations, and research capacity [47]. Irrespective of approach, recruitment procedures need be reflective of input from the target population (AYA) to increase the efficiency, reach, validity, and scientific yield of HIV prevention research [48]. Moreover, greater collaboration and resource sharing among researchers, academic and clinical institutions, and community partners will ultimately provide the needed infrastructure for development of tailored, evidence-based recruitment models and approaches lending to health equity for AYA.
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Funding
Support for preparation of this manuscript was provided by the New York University P20 Exploratory Center for Precision Health in Diverse Populations, Rory Myers College of Nursing. Dr. Navarra is supported by the National Institute of Nursing Research (R01NR019535-01): Adherence Connection Counseling, Education, and Support (ACCESS) II Clinical Trial.
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Appendices
Appendix 1. CDC Compendium of Evidence-Based Interventions and Best Practices for HIV Prevention. Age Range 13–34 years old
HIV Prevention
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HIV Diagnosis
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Outbreak Response
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Navarra, AM.D., Handschuh, C., Hroncich, T. et al. Recruitment of US Adolescents and Young Adults (AYA) into Human Immunodeficiency Virus (HIV)–Related Behavioral Research Studies: A Scoping Review. Curr HIV/AIDS Rep 17, 615–631 (2020). https://doi.org/10.1007/s11904-020-00530-1
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DOI: https://doi.org/10.1007/s11904-020-00530-1