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Pharmacist and patient perspectives on recruitment strategies for randomized controlled trials: a qualitative analysis



Although recruitment is a major challenge for most randomized controlled trials, few report on the difficulties of recruitment, or how it might be enhanced. The objective of our study was to qualitatively explore the experiences of both patients and pharmacists related to recruitment for ACCESS, a large trial involving low-income seniors, given that two of our most successful recruitment strategies were direct patient recruitment materials and use of community pharmacists.


Using qualitative descriptive methods, we collected data from pharmacists and study participants. Pharmacists were asked about their impressions of the study, as well as challenges they faced and methods they used to recruit potential participants. Focus groups with trial participants centered on the patient recruitment materials. Interviews and focus groups were recorded, transcribed and analyzed using thematic analysis.


Pharmacists noted that their first impressions of the study were positive as they described being enticed to help the study team by the potential benefit of copayment elimination for their patients and the low time commitment. Pharmacists noted they were more likely to recruit if they were well informed on the study, as they could answer their patients’ questions. Participants noted that their primary motivations for participating were the tangible benefits of free medications and the intrinsic value of participating in research.


We noted that recruitment through pharmacies was an effective method as most patients have trusting relationships with their pharmacist. To optimize recruitment through pharmacies, study procedures should be straightforward, and pharmacists need to be equipped with good knowledge of the study. When promoting a study to potential participants, messaging should ensure the individuals are aware of the tangible benefits of participation while still presenting a full overview of the trial.

Trial registration

Trial Registration Number: NCT02579655 – initially registered Oct 19, 2015.

Peer Review reports


Randomized controlled trials (RCTs) are considered the most robust study design in health research and can reduce much of the bias inherent in observational study designs [1]. Investigators often underestimate the time, costs, and difficulties involved with recruiting trial participants, as only 55% of RCTs reach their pre-specified recruitment targets [2]. Difficulties with recruitment can lead to delays, cost overruns [3], and potentially a resultant lack of statistical power [4]. Several review articles have highlighted the need for improved recruitment efficiency with suggestions for general techniques to enhance recruitment such as phone call reminders, ‘opt-out’ recruitment methods, or financial incentives, but these methods are not universally applicable [5,6,7].

Health care professionals outside of the immediate research team can be effective in recruiting patients due to pre-established relationships with patients who are potential study participants [8, 9]. Pharmacists have been suggested to be especially helpful in recruiting participants [10, 11], particularly for community-based trials, or those that focus on medications or adherence.

Another means of recruitment used in many RCTs is patient-facing self-referral materials. It remains uncertain what types of messages are most impactful for attracting patients to enroll in research. Some studies have suggested that incorporating participant feedback when creating materials might assist in recruitment, as participants may provide insights that were not considered by study staff [12]. Obtaining participant input early on in studies could potentially save both money and time by improving recruitment efficiency [13].


Study aims

Since pharmacists and patient-facing materials were among the most commonly used methods for recruiting for our community-based clinical trial, our objective was to use qualitative methods to better understand participants’ and pharmacists’ experiences with the recruitment process within the context of a large community-based RCT. Additionally, given the importance of patient input into recruitment activities, we sought feedback on recruitment materials from participants in order to inform subsequent recruitment efforts. While the use of these particular methods to recruit participants for a randomized trial is not novel in itself, conducting a qualitative descriptive study to explore perceptions of both patients and recruiting pharmacists on recruitment processes is seldom reported and has the potential to make a meaningful contribution to the literature and enable these two strategies to be used more effectively in future research.

Study context

The Assessing outcomes of enhanced Chronic disease Care through patient Education and a value-baSed formulary Study (ACCESS) is an ongoing 3-year randomized controlled trial evaluating the impact of two interventions on cardiovascular endpoints in Alberta, Canada [14] ( Identifier: NCT02579655). Eligible participants were low-income (<$50,000 CAD/year) adults 65 years of age or older, with at least one cardiovascular-related chronic health condition, and Alberta Blue Cross Seniors’ Benefit coverage, allowing premium-free access to most medications with a 30% copayment. ACCESS is a factorial (2 × 2) trial studying the following interventions: (1) a medication copayment elimination plan whereby participants received all high value cardioprotective medications without copayment, and (2) a self-management education program individually tailored to each participant [14]. Recruitment for the ACCESS Trial began in November 2016 and concluded in September 2018, with follow-up ongoing, and expected to be complete in mid-2021.

Participants enrolled in the ACCESS study by receiving initial information about the study in the community – through a number of sources, including pharmacists, physicians, outreach activities and media. Regardless of the means by which a participant heard about the study, they were directed to call a central study telephone line where they were then screened for eligibility, after which they completed written informed consent and baseline questionnaires before being randomized. We recently published a detailed retrospective examination of the various recruitment strategies utilized to enroll more than 4000 participants in the ACCESS trial [15]. We found that pharmacists recruited 38% of participants. However, this strategy was also relatively resource intensive, costing over CAD$150,000. The vast majority of ACCESS participants were enrolled either through pharmacies (where recruitment materials were present) or by encountering recruitment materials such as brochures and posters in other locations such as community centres, medical offices, churches, seniors’ centres, recreational centres, and shopping malls – accounting for another 43% of our participants [15]. Given the importance of these two recruitment methods for helping us achieve our target sample size, we decided to focus this qualitative study on exploring these two methods in greater detail.

Study design

This study used qualitative descriptive methods [16], which aim to describe phenomena in the everyday terms of the participants [17]. Our objective was to explore the perceptions of the recruiting pharmacists and trial participants with regards to the reasons underlying successes and challenges with recruitment in ACCESS. Both the ACCESS trial and this qualitative exploratory substudy have been approved by the University of Calgary Conjoint Health Research Ethics Board.

Sampling & Data Collection

We collected data using individual semi-structured interviews (with pharmacists) as well as focus groups (with study participants). The pharmacists were sampled purposively [18] from the 855 pharmacies that recruited for ACCESS. Enrollment was limited to pharmacists who recruited at least one participant, but was not limited by geographic location within the province. The strata used for purposive sampling included the variables reported in Table 1. Sampling continued until saturation [19], meaning no new themes or codes emerged from additional interviews. Interviews, ranging in duration from 20 to 50 min, were conducted by telephone in the spring of 2018 [20] by a research assistant (JMF) who was trained in qualitative interviewing. JMF also recorded field notes. Interviews were recorded and professionally transcribed verbatim. A question guide was used to ensure similar material was covered during each interview (Supplemental Material 1). The pharmacists were informed of the purpose of the study at the enrollment and consent stage.

Table 1 Characteristics of Pharmacists (n = 20)

In the spring of 2017, two in-person focus groups, each lasting 2 h, were held with participants who had enrolled in ACCESS during the preceding 6 months. The purpose of these groups was to inform the researchers about the recruitment materials and to refine techniques and messaging. The two groups were drawn from the two intervention arms in the ACCESS trial; individuals within each group were selected through purposive sampling based on age, gender, and income. As the purpose was to obtain feedback on the recruitment materials, individuals recruited by pharmacists and by friends/family members [15] were not included, as they may have been told about the study without having seen the printed materials. Only participants situated close to Calgary were invited to minimize travel requirements. Focus groups were facilitated by TSS and DJTC (Supplemental Material 2). Focus group proceedings were digitally recorded and transcribed verbatim. Field notes were recorded during focus groups and written documentation was retained by the study team. The participants were informed of the purpose of the study at the enrollment and consent stage.

Data analysis

Transcripts from interviews and focus groups were imported into NVivo 12 software (QSR International, Doncaster, Australia) for management of the qualitative data. Thematic analysis techniques were used to code the data [22]. The initial coding template was based on the interview guide, and additional categories were added inductively through open coding, which was completed independently by JMF and TSS, and then reviewed with DJTC. Focused coding was completed by reviewing all the codes and collapsing them into groupings.


Study sample

Initially, 27 pharmacists were approached for an interview, with 20 agreeing to participate, and 7 declining due to time commitments or not meeting the criteria of having recruited at least one participant. After 20 interviews were completed, saturation had been reached and we decided to discontinue pharmacist interviews. The pharmacists had a relatively even distribution across the criteria used for purposive sampling (Table 1). 38 participants were contacted for the focus groups. Of those, 17 agreed to participate, and 14 attended the focus groups (Table 2). We present our results based on the type of participant: first barriers and facilitators related to pharmacists, followed by patient-level feedback. Results are supported by quotes in Table 3.

Table 2 Characteristics of Focus Group Participantsa
Table 3 Quotes from Qualitative Interviews and Focus Groups

Pharmacist-level: barriers, facilitators, and recruitment methods

Pharmacists’ barriers to recruitment

A prerequisite for pharmacy recruitment is for pharmacists to hear about and understand the purpose of the study. There were some challenges disseminating knowledge about the study to the participating pharmacists. Nearly all pharmacists had a solid understanding of the objectives of the study: “It was something to do with if there was a difference between people having coverage for chronic medications versus the ones that don’t … [with regards to] compliance and overall medical medication control” (Rx12). However, there were apparent gaps in knowledge regarding the group allocation and enrollment procedures. Most had sufficient knowledge regarding the copayment elimination intervention, but fewer understood the education program.

One of the most common barriers that pharmacists cited was lack of patient follow-through once referred on to the study. They reported discussing the study with patients but suspected that many patients would not follow through with enrollment after their initial discussion. Pharmacists also discussed logistical issues with recruitment, including having to engage all other pharmacy staff members in recruitment. Another concern was a lack of time: “you have such limited time with the patient, what are the things you are going to bring up and talk about and sometimes [the study]‘s one of them and sometimes it isn’t” (Rx13). Some pharmacists also identified that the way materials were displayed within pharmacies limited their utility and presented a barrier.

Facilitators and strategies for pharmacist engagement

Having adequate knowledge about the trial was a key step in helping pharmacists recruit. Pharmacists described becoming aware of the ACCESS trial from a number of different sources including: (1) ACCESS study staff, (2) colleagues, (3) corporate management, and (4) patients/study participants.

In order to engage in the recruitment process, not only do pharmacists need to know about the proposed research, they must also see value in it. Many pharmacists described that they were interested in recruiting because the study offered additional support for their patients who were facing challenges. The education intervention was an added benefit for some pharmacists, but the main driver of engagement was the potential for patients to receive free medications. Some pharmacists also specified that they thought the intervention was likely to improve adherence: “Sometimes they cannot afford the medications, they say ‘no I don’t want this one’. Sometimes they do not take it every day, just on and off. When the patient has to pay nothing, zero, they will show more compliance to the treatment” (Rx15). In addition to these tangible benefits to their patients, several pharmacists also expressed interest in the scientific merit of the study. Numerous pharmacists also mentioned that a factor in their decision to participate was the ease of participation, and the fact that very little was required of them, with the study team completing the enrollment procedures.

Methods for recruiting patients

Pharmacists utilized several methods for recruiting patients, which we categorized into ‘blanket strategies’ and ‘targeted strategies’. Blanket recruitment included handing out brochures to all patients in their pharmacy, or putting up posters in waiting areas: “you know I have a corner there for people to wait for their prescriptions and have coffee and it has your poster there” (Rx14). Targeted recruitment included speaking directly to potentially eligible patients. Often pharmacists put brochures directly in the medication bags of patients they thought might be eligible: “When we filled prescriptions of some of the patients that we thought would be good candidates, we tuck in, so when they picked it up they got that” (Rx1). The factors pharmacists considered in their targeting included: financial issues, lack of education, baseline chronic conditions, and adherence issues. They cited that they looked for these factors because of trial eligibility criteria and also because they knew that these patients were those who were most likely to be interested in enrolling in the trial.

Most pharmacists at least employed a blanket approach by putting out posters or brochures. Whether a pharmacist elected to additionally use a targeted approach depended upon whether he/she had trusting professional relationships with patients. Additionally, targeted approaches were easier for pharmacists who regularly undertook medication reviews with their patients. When pharmacists wished to delegate recruitment to a technician or student, they used only general, blanket approaches to recruitment, minimizing the need for detailed knowledge of the patients. Many pharmacists described using a combination of both blanket and targeted recruitment to introduce the study to patients: “[Patients] would take off the tab and if I see somebody doing that or taking a picture of the poster I would hand them the leaflet and say, ‘here, keep this too and this is what the study is all about’ and just give them a rundown.” (Rx17).

In addition to these routine techniques that were suggested by the ACCESS team, several pharmacists developed novel self-directed strategies to recruit patients, unbeknownst to the study team. These methods included using radio advertisements, newspapers and social media, and community events.

Participant-level: barriers, facilitators, & recruitment material feedback

We categorized responses regarding patient-level experiences into similar themes as above: (1) patient-related barriers to recruitment; (2) facilitators to enrolment for participants; and (3) specific suggestions about the patient-facing study recruitment materials.

Participant barriers to enrollment

Many of the barriers described by patients, or perceived by pharmacists, stemmed from potential participants not fully understanding details about the study after their initial interactions. For example, one participant thought that he needed to access a computer in order to enroll, which was not the case. Language-related barriers contributed to this lack of knowledge, as study materials were only presented in English. Similarly, a participant identified that some individuals belonging to cultural and linguistic minorities may not have understood recruitment materials. Some participants were somewhat skeptical, or suspicious, about research. A pharmacist identified that some patients were concerned about the implications of being in a ‘trial’: “[Patients’] initial ideas [about] any trial is that you will be popping pills that they don’t know” (Rx17). Another issue identified by both participants and pharmacists was that the benefits offered by the study might only appeal to those in need of financial assistance. A participant stated the study “would only appeal to those whose costs aren’t covered” (Pt14) and this sentiment was echoed by pharmacists as well. Finally, the logistical arrangement for recruitment contributed to participants’ difficulty enrolling, as patients needed to take the initiative to call the study enrollment centre. One of the more commonly identified barriers was that patients would forget about the study before having a chance to call in, which was also a concern identified by the pharmacists: “they might seem gung-ho here, but by the time they get home and set it on the table, life goes on and you sometimes wonder how many people actually call” (Rx13).

Facilitators to participant enrollment

The initial step in getting patients enrolled for a clinical trial is for researchers to generate interest within potential participants. Not unlike pharmacists, participants reported two major reasons for being interested in ACCESS: the direct benefits of the interventions, and the intrinsic value of the research. Most participants commented on the benefit of the additional medication coverage but, prior to enrollment, few participants saw the education program as being a major factor.

In addition to the direct benefits of the interventions, several participants mentioned that they chose to participate because of the value of the research – because it could benefit society, or because they derived some other benefit from it. Societal benefit included participants having altruistic motivations in advancing research that could benefit their peers. Personal benefit focused on the knowledge participants could gain through the study. Some participants expressed the opinion that these ‘intrinsic benefits’ were unlikely to be the true motivations behind participation, but that the underlying reason was the potential for receiving additional medication coverage: “I mean we try to be holier-than-thou but it’s the free medication that we are all here for, and I think that’s going to be a big grabber for a lot of people.” (Pt2).

Once individuals became interested, they still faced numerous challenges and barriers to following through with enrollment, as described above. Pharmacists reported using several strategies to help patients overcome these barriers. Rather than simply giving out brochures, pharmacists felt they were more likely to be successful by speaking with patients directly: “if you just give it to them and don’t explain it, they are most likely not to phone the number that’s on there.” (Rx5). Often the solution was to encourage the patient to call in, referencing the potential benefits of the medication coverage.

A number of other factors helped individuals overcome barriers to recruitment. Several participants recounted receiving encouragement from family members to become involved in the study. Others indicated that the involvement of a trusted institution engendered a sense of legitimacy: “The University logo gives it credibility.” (Pt6). This sense of trust was also seen with pharmacists: “You see that it’s through the [University] so you know it’s a reputable study.” (Rx11). Furthermore, the straightforward and clear manner in which the study was explained to participants made them more likely to participate: “[The article] was telling the facts, why you did the research and [how study staff] were going to go about it and it seemed to have no hidden agenda(Pt13).

Recruitment material suggestions

One purpose of the focus groups was to improve the appeal of the recruitment materials, therefore, participants were asked for direct feedback about the posters and brochures. While the overall impression was generally positive, there were concerns about various aspects of the materials. Some felt the messaging was not fully transparent about the fact that receiving medication coverage was not guaranteed. It was also noted that some of the language on the materials could be better explained, such as ‘senior’ (“there are seniors 55 years old and it’s not going to cover them(Pt3)) and ‘chronic disease’. The small size of the font was also mentioned as a concern for this population.

Participants were asked to evaluate various strategies and messages. They preferred messaging promoting the possibility of a benefit to them (e.g. “New study: providing free medication coverage & personalized health education”) over messaging focused on empowering them to feel like they are contributing to something beyond themselves (e.g. “Seniors can help improve health care costs”). Participants preferred messaging about medication copayment coverage over messaging around the education program. Participants also preferred messaging that portrayed their individual importance to the research (e.g. “Seniors needed”) above more generic calls (e.g. “Get involved”).


Our findings support the importance of collaborative relationships between investigators and recruiting pharmacists. When engaging pharmacists to help with study recruitment, we learned that it is important to educate them on all facets of the study. In community-based trials like ACCESS, pharmacists helped recruit on a voluntary basis, and were not formal members of the study team, therefore it was not reasonable to expect them to know the study protocol as if they were team members. However, having a more in-depth knowledge of the study seemed to be beneficial to promoting recruitment. Both targeted and general recruitment strategies employed by pharmacists were thought to be effective. Pharmacists can help patients overcome hesitation to enroll in trials through direct conversations and encouragement. Patient-facing recruitment materials focusing on the potential tangible benefits were most impactful (as opposed to materials focusing on the social value of research). Study messaging needs to be clear and should not be perceived as misleading. Participants face a number of barriers to enrollment in research studies, and researchers can leverage clear communication techniques and the credibility of their institutions to engender trust with potential participants.

The use of pharmacists was an invaluable method of recruitment for the ACCESS trial [15], as has been documented in other trials [24]. Utilizing pharmacists allowed us to leverage pre-existing relationships they had with patients. Pharmacists who believed that involvement in the study would be beneficial to their patients were more motivated and effective recruiters. Because of their pre-existing trusting relationships with their patients [25,26,27,28], pharmacists were able to act as mediators in providing prospective participants with key information that enabled their recruitment. Most pharmacists were busy, yet many took the time to present the study to their patients in a positive manner due to the potential benefits for patients. When the benefit to patients is in question, others have found that recruitment is challenging and may potentially be compromised by the predetermined opinions of the providers tasked with recruitment [29]. Working with recruitment partners to address concerns and facilitate full support early on can also aid in recruitment, as suggested in our findings and in other studies [30]. The following considerations may enhance pharmacist-led recruitment: (1) The investigators must ensure that pharmacists are provided with the tools and opportunities to gain reasonable knowledge of the study aims and procedures; (2) Participation in recruitment should entail minimal workflow disruption; (3) There should be a potential benefit, both to patients and pharmacists; and (4) Closed-loop communication should exist between the study team and recruiting pharmacists regarding the enrollment of their patients. The utilization of numerous methods of introducing pharmacists to the study was beneficial, as several pharmacists described hearing about the study through multiple channels (e.g. study staff, colleagues, and patients). Pharmacists were a natural fit to assist with recruitment for the ACCESS trial, however, other health care professionals were also involved in recruitment to a lesser degree [15], and many of the principles outlined above would apply to these providers as well.

While involving pharmacists or other providers may help with enrollment, the importance of employing multiple strategies, such as direct advertising to the public, should not be overlooked. Studies have shown that most potential participants who encounter recruitment materials never actually enroll [31], although the reason why is rarely apparent [32]. Our study explored patients’ reasons for enrolling, and we suggest that investigators use clear communication strategies in recruitment materials, emphasize potential benefits to participants, and leverage the credibility of their institution’s reputation. Using a combination of these methods was found to be effective for the ACCESS trial. In particular, it can be useful for researchers to know what benefits would be of greatest interest to participants. In the ACCESS trial, the potential for enhanced medication coverage was considered to be a greater benefit than the educational program, and we found that recruitment materials focusing on the possibility of receiving this coverage were better received by potential participants. Several participants raised issues with recruitment materials because of language or cultural issues. Where possible, investigators should try to make recruitment messaging as accessible as possible for the target population. In the ACCESS trial, however, we decided that in order to benefit from the patient education intervention an individual had to be conversant in English anyway, so language tailoring of recruitment materials was not undertaken in our case.

Other clinical trials have examined the effects of their recruitment methods. Similar to our conclusions, one study recommended the use of plain, objective language, keeping personal biases out of discussions, and maintaining clear communication [33]. Another study found that travel inconveniences were a major reason for participants not wanting to become involved [34] – this was not an issue in the ACCESS trial as enrollment and follow-up was done remotely. Another study which explored recruitment qualitatively discussed the importance of obtaining patient feedback to improve recruitment early on in the trial, supporting our conclusions on the utility of this qualitative approach [30]. Others have noted that the main reason for participation in a clinical trial is self-interest – including financial incentives [35] with minimal evidence of altruistic motivation [36]. While one participant noted that it was likely that most participants were motivated by self-interest rather than altruism, many participants did cite altruistic motivations. The altruistic motivation is supported by previously published literature in which both the benefit to science and general altruism have been raised as reasons for study participation [37].

This study has some limitations. First, the main focus was on recruiting through pharmacists, specifically. However, the themes that emerged are likely true for engaging other health professionals who have existing relationships with potential participants. Second, it is possible that the established relationships between the pharmacists and the study staff might have influenced responses to the interview questions – however, it’s important to note that there were hundreds of pharmacies recruiting for ACCESS, so study staff had relatively infrequent contact with individual pharmacists. Third, the generalizability of our findings is limited, as the ACCESS study included only low-income seniors from Alberta who were being offered a chance to receive a direct financial benefit. Due to the fact that this study was conducted in Canada, where the healthcare system is unique in that universal coverage of pharmaceuticals is not guaranteed and those who have coverage often face copayments for medications [38] there may be limited applicability of the ACCESS intervention to systems outside of Canada. Whether these findings would apply to other trials in different contexts is unknown, but there are likely to be transferrable elements. Fourth, the relatively small sample size of the focus groups may have hampered our ability to achieve complete saturation. Finally, as the intention of the focus groups was to gain feedback on recruitment materials, participants who were recruited using other methods were excluded. This precluded us from obtaining patients’ detailed feedback on alternate recruitment methods (e.g. radio). Despite these limitations, this study adds to the previously published literature through the use of detailed qualitative methods, which have seldomly been used to investigate recruitment success and challenges [30]. We were able to capture richness and detail that is not possible in the quantitative studies or meta-analyses which have been previously published on this topic.


Our findings will be of interest to investigators seeking to recruit a large number of older adults for pragmatic clinical trials. Future research should address recruitment processes across diverse demographic categories and study designs. In addition, investigators should consider including details regarding recruitment within publications, as few currently report on recruitment struggles. Considering that recruitment is a concern for all RCTs, proactively addressing these issues has the potential to decrease costs, increase enrollment, and reduce time taken to meet recruitment goals.

Availability of data and materials

The dataset used and/or analyzed during the current study may be made available from the corresponding author on reasonable request.



Assessing outcomes of enhanced Chronic disease Care through patient Education and a value-baSed formulary Study


Randomized Controlled Trial


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We would like to acknowledge all of the recruitment efforts and assistance from the ACCESS staff members: Sophia Tran, Alexa Desjarlais, Charlotte Martin, and Craig Curtis. Eshleen Grewal and Sheila Crombie helped with formatting and references of this manuscript. We would also like to thank all of the pharmacists and the participants who took part in the interviews and focus groups.

Other declarations

The interviewers conducting the interviews and focus groups had the following qualifications: JMF, BSc., the research assistant, had been trained in conducting qualitative interviews; TSS, BSc., the research coordinator, had previous experience conducting qualitative research; and DJTC, MD PhD., the study’s principal investigator, had previous experience both conducting and supervising qualitative research. Of the interviewers conducting the qualitative research, JFM and TSS are female, and DJTC is male.


The ACCESS trial was funded by Alberta Innovates-Health Solutions (CRIO Program), the University of Calgary Clinical Research Fund, and the Canadian Institutes of Health Research - Foundation Grant (Manns). Dr. Campbell’s salary was supported by a Clinician Fellowship from Alberta Innovates. Ms. Fletcher’s salary was through the ACCESS trial’s funding. The funders had no role in data collection, analysis, interpretation, or writing of this manuscript.

Author information

Authors and Affiliations



JMF: Conceptualization, Data Curation, Formal Analysis, Investigation, Methodology, Visualization, Writing – Original Draft, Writing – Review & Editing; BJM: Conceptualization, Funding Acquisition, Resources, Supervision, Writing – Review & Editing; RT: Conceptualization, Writing – Review & Editing; BRH: Conceptualization, Writing – Review & Editing; MT: Conceptualization, Writing – Review & Editing; TSS: Conceptualization, Data Curation, Formal Analysis, Investigation, Methodology, Writing – Review & Editing; DJTC: Conceptualization, Data Curation, Formal Analysis, Investigation, Methodology, Visualization, Writing – Review & Editing. All authors read and approved the manuscript.

Corresponding author

Correspondence to David J. T. Campbell.

Ethics declarations

Ethics approval and consent to participate

The University of Calgary Conjoint Health Research Ethics Board approved both the participant focus groups and the pharmacist interviews, within the purview of the ethics certificate for the ACCESS Trial: REB13–1241. Pharmacists were consented verbally over the phone, and focus group participants gave written consent.

Consent for publication

Not applicable - no identifying data is present.

Competing interests

The only disclosure is that Dr. Tsuyuki has received investigator-initiated grants from Merck Canada, AstraZeneca Canada, and Sanofi Canada. He has given paid presentations for Merck Canada and Sanofi Canada. These grants and presentations are unrelated to the current manuscript. This manuscript has not been submitted for publication in any other journal.

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Supplementary information

Additional file 1.

Interview Guide - Assessing outcomes of enhanced Chronic disease Care through patient Education and a value-baSed formulary Study (ACCESS).

Additional file 2.

Agenda - ACCESS Study-Recruitment material Focus Group.

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Fletcher, J.M., Saunders-Smith, T., Manns, B.J. et al. Pharmacist and patient perspectives on recruitment strategies for randomized controlled trials: a qualitative analysis. BMC Med Res Methodol 20, 270 (2020).

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