A qualitative study on consenting approaches for genomic research in communities with low literacy

Background: Low literacy of study participants in Sub Saharan Africa has been associated with poor comprehension during consenting process in research participation. The concerns in comprehension are far greater when consenting to participate in genomic studies due to the complexity of the science involved. While efforts are made to explore possibilities of applying genomic technologies in diseases prevalent in Sub Saharan Africa, we ought to develop methods to improve participants’ comprehension for genomic studies. Aim: The aim of this study was to understand different approaches that can be used to seek consent from individuals with low literacy in Sub-Saharan African countries in genomic research to improve comprehension. Methods: Using qualitative study design, we conducted focus-group discussions, in-depth interviews and participant observations as data collection methods. This study was embedded in a hospital based genomic study on Sickle Cell Disease at Muhimbili National Hospital in Tanzania. Thematic content analysis was used to analyse the transcripts and field notes. Results: Findings from this study show that literacy level has little influence on understanding the research details. According to the participants of this study, the methods used to provide information, the language, and time spent with the study participants were the key factors influencing understanding. The availability of group sessions held before individual consent to allow for a detailed questions and answers format was agreed to be the best method to facilitate the comprehension. Conclusion: The quality of the consenting process of participants will be influence by a number of factors. The type of research consented for, where the research will be implemented and who are the potential study participants are amongst the factors that need to be assessed during the consenting. Measures to improve participants’ comprehension need to be developed when consenting participants with low literacy level in genomic studies.

consent for genomic studies when implemented in Sub-Saharan Africa (SSA) is challenging to the researchers and research participants [4][5][6][7][8]. Often low literacy of the participants has been associated with poor comprehension during the consenting process [9,10]. The challenges are linked to difficulties in providing information in a comprehensible manner to the participants considering the complexity of the science involved [11,12]. The process of interpretations and translations of key concepts into accessible terms for the participants can be challenging to achieve for researchers and field workers [6,13]. This is particularly problematic in populations where the science requires translations into local languages [2,[14][15][16]. Lack of training in genetics for clinicians and the shortage of genetic counsellors in the SSA may have increased the difficulty in communicating the information to the research participants [17]. Often in this context, a well-written and signed consent by a participant does not guarantee understanding. In contributing to that discussion, we designed an exploratory study aiming to understand research participants' perspectives and experiences when consented in a genomic study implemented in SSA. We were particularly interested to learn how participants' literacy level may have had an influence on their understanding the details of the research into which they have enrolled.

Methodology Sampling and recruitment
We recruited research participants enrolled in an urban hospital-based study aiming to understand genetic determinants of clinical heterogeneity of sickle cell disease (SCD) in Tanzania [18,19]. At the time of recruitment, the study consisted of 3751 individuals with SCD, 1779 were between 5-17 years of age with almost a 50/50 gender distribution [20]. Participants for the study reported here, were recruited through adult and paediatric clinics at Muhimbili National Hospital. Purposive sampling was used to select individuals willing to provide detailed information about their understanding and experiences of being enrolled in the study. In total forty-three (n = 43) participants were recruited into our study. We defined literacy level in relation to the number of years spent in school as per education system in Tanzania; (1) Primary -basic level of education, also included here were participants with no formal education (n = 23); (2) Secondary level -intermediate level (n = 16); and (3) Tertiary level -high level of education (n = 4).

Data Collection Methods
Data was collected through focus-group discussions (FGDs), in-depth interviews (IDIs) and participant observations (POs).

Focus Group Discussions (FGDs)
Five FGDs were conducted with six participants in each of the groups. The composition of the FGDs took into consideration age, level of education, and gender. The FGD guide was designed to facilitate a semi-structured discussion around participants' experiences, challenges and possible ways to improve the consenting process. In total, 30 individuals participated in the five FGDs. Participants included were adult SCD patients enrolled in the study. Details of the participants' descriptions are provided in Table 1.

Participant Observations and In Depth Interviews
In addition to the focus groups, we observed the consent process of six new participants who were enrolled in the study during the period of our research. The content of the observation checklist was developed based on the consent form used by the researchers. For instance, we observed how the researcher communicated the objectives and methods of the study to the participants as described in the informed consent. After observing the consenting process, we interviewed those participants (IDIs) to gather their perspectives on the consenting process. In total, 13 IDIs were conducted, out of which seven (7) IDIs were conducted with research participants who were already enrolled in the study. Amongst the participants, nine were parents of children who have been enrolled in the SCD study. Participants were aged 24 to 43 years old, amongst which two (2) were men and eleven (11) women. Since most of the children were brought to the clinic by their mothers, we did end up interviewing more women than men in the study. Details of the participants' descriptions are provided in Table 2.

Data Analysis
We analysed the transcripts and field notes using thematic content analysis adapted from another qualitative study implemented in Tanzania, Ghana and Cameroon [21]. The first author, (DB), collected all the information for IDIs and FGDs as well as recording participants' observation checklist.
The interviews were all done in Swahili and then translated to English after the analysis stage.

Results
Three main themes were identified from our analysis of the data from FGDs, IDIs and POs: 1) Relationship between low levels of literacy and the achievement of informed consent; (2) Factors contributing to poor understanding included: inadequate information provided to the participants, age at enrolment, and time spent by the participants; (3) Possible ways to improve understanding as suggested by participants; opportunities to ask questions and group information sessions followed by individual consenting.

The relationship between low levels of literacy and the achievement of informed consent
Participants who reported having no formal education and those categorized as having low literacy felt that the possibility of gaining a good understanding of the research was not influenced by having low literacy level. This perception was consistent during the IDIs, FGDs and POs. The following quotations illustrate this.
A response from a mother (IDI 3) who doesn't know how to read or write was, "Research in Sickle Cell Disease are [is] done to understand the cure and find solutions on this problem" IDI 3, interview with a mother of a child with Another example was also from a mother (IDI 1) who has not received formal education, she explained, "Research is an investigation to understand about a certain disease problem in-depth or look for a cure of a certain disease"" IDI 1, interview with a mother of a child with SCD enrolled in the genomic study In one of the FGDs, participants were asked whether the information provided by researchers was easy or difficult to understand. One FGD member began, "Yes, it is easy to understand, [A probe was followed after his response, Is it easy for you because you are a college graduate? ] Another participant in the group with no formal education replied, "It is all about the individual person and has nothing to do with the level of education" focus group discussion 2 with adult SCD patients enrolled in the genomic study A participant in another FGDs claimed, "I am not concerned by the type of information provided, it is not a problem for me to understand, we need to be educated more on the research and understanding will not be a problem" focus group discussion 3 with adult SCD patients enrolled in the genomic study A few participants believed that education plays a major role to be able to understand the information.
One noted, "It is true that for someone to understand this (research) information, it will depend on the individual person, but also the level of education they possess" IDI participant 5, 43 year-old men with SCD who was newly enrolling in the genomic study Factors contributing to poor comprehension of the research 1. Adequacy of the information provided to the participants The majority of participants for both the IDIs and FGDs felt that research information was not adequately provided. Participants describe the quality of the interactions, "You need more time to understand the information and if you are not keen enough you will not be able to understand, time given was so short and answers were given in a rush [ed] way" IDI participant 9, mother of a child with SCD enrolled in the genomic study A FGDs respondent clarified, "The truth is we are not getting enough information from the doctors [researchers] and education is not being provided to our satisfaction [on the research], only the progress of your disease, but nothing more...that is at least my personal view" Focus group discussion 1 with adult SCD patients enrolled in the genomic study One explanation the participants gave for why they had received inadequate information was an increase in patient load in the clinics, "I do not think we are now getting information as it used to be, as time goes by the number of clinic visits decreased and the time to stay with a doctor also has decreased" Focus group discussion 2 with adult SCD patients enrolled in the genomic study In contrast to the other study participants, however, one woman noted, "I have been provided with detailed information about the research, they have even come to my house to do research and the experience at home was quite good" IDI 7, interview with a mother of a child with SCD enrolled in the genomic study.

Age at enrollment
Age at enrolment was considered to be a factor by some of the participants for not recalling the information provided during the consenting process. Since participants were recruited from a cohort study, this was only relevant for those who were enrolled in the study by their parents or caretakers when they were young. As In addition to preferring a two-stage general informational session and an individual consent signing process, participants preferred face-to-face encounters to getting information from a video, this comment was raised when participants were asked about having videos in the clinics to explain the study, "I am sceptical with the video method of providing information, I am not sure of it, it depends on the research type, you just cannot show everything" focus group discussions 1 with adult SCD patients enrolled in the genomic study Discussion When we began this research, we expected low literacy to be one of the factors hindering comprehension at the time of consent to participate in genomic research. However, our findings and the analysis of our data have shown that participants believe that understanding of the concepts in genomic research were dependent more on the methods used to communicate the information [22]. These results were similar to those of a study conducted in Gambia and Bangladesh [10,23,24]. which indicated that ways in which information is provided is the most important component influencing success of the consenting process.
Limitation of time was also a contributing factor for researchers not to adequately provide information. Group interactions were thought by participants as very helpful to assist them recall the information and provided them with opportunities to ask any questions they have to the doctors as compared to the one-on-one session. In addition to that, the group sessions before one-to-one sessions will help minimize time the researchers will spend with individual participant to explain the research.
Although participants acknowledged that asking questions can enhance comprehensions, only few participants felt comfortable asking questions about the research. Fear of being seen as ignorant, trusting that doctors know it all and the power imbalance between the researcher and the subject especially when the doctor is also the one recruiting subjects limit participants willingness to ask questions [14,[25][26][27]. One way of addressing this is might be by having the research team different from the clinical team.
Participants who enrolled in the study when they were young could not recall the information provided during the consenting process. Some vaguely recall their parents consenting on their behalf. This explains the importance of re-consenting study participants after a certain time period depending on the study's risk level and duration. The re-consenting process emphasized is not just asking participants if they are willing to continue being part of the study, but rather refreshing on the purpose of the study, procedures involved, risks as well as benefits of the research.
In our interviews and focus groups, in addition to highlighting challenges, participants suggested alternate research presentation methods that could be used to improve the effectiveness and accessibility of consent processes. Suggestions made included the use of practical examples and simple terminologies that can be easily understood by the participants [28] [29]. Participants in this study felt that the quality of the information provided was compromised by the limited time doctors have to spend on the consenting process. It was felt that providing information in groups through seminars, in the presence of nurses or doctors as moderators, would help to save time required during the one-on-one session. In-group sessions, the researcher may try to ensure all the general components of the informed consent such as purpose, risks, procedures, benefits and dissemination plans are explained in detail [30]. By using a group session approach, researchers who may also be physicians, will not be required to spend a lot of time explaining research to individual participants. This particular arrangement will not substitute individual autonomy because the aim will be to empower the subjects to make the right informed decision, after understanding the study details. This is also supported by a study done on tailoring consent to context [23], that in some settings individual consent may benefit from being preceded with providing information in groups. However, there are studies that suggested that there were no overall benefits of providing information in groups before individual consent [31].
Since this study was done in a hospital setting, participants sometimes seem to confuse research methods and clinical practices. At times it was difficult to tell whether the experiences they were referring to, were research or clinical experiences. We also acknowledge that the experiences shared by participants in this study do not seem to be specific to genomic research, and, therefore, the findings can be broadly interpreted to other non-genomic research.

Conclusion
This study afforded us with an opportunity to reflect on what kind of information is being provided to the participants and how. Our findings suggest that the reason why comprehension is difficult is not solely due to low literacy of the participants but also, perhaps mostly, down to how the information is being provided. Researchers conducting research in the low-literacy settings have to invest in understanding the best methods to use to provide the research information in a much more accessible and comprehensible manner. Participants' low literacy levels have always been used as a scapegoat for poor comprehension, but by placing the blame on participants we have failed to acknowledge our failure to consider the context and adequately provide clear explanations of our research. Our recommendation to researchers is to plan the consenting process ahead of time and plan for a re-consenting phase for studies that have a long time span, to factor in the context of where the research will be carried out, and to better understand the needs of the target population to and align their needs to efforts to fully inform the consenting process. reviewing the manuscript. LP, SN, MP assisted in revising the manuscript. All authors reviewed and approved the final manuscript.