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Abstract
Objectives 1.5 million people in the UK have mild to moderate learning disabilities. STIs and bloodborne viruses (BBVs) are over-represented in people experiencing broader health inequalities, which include those with mild learning disabilities. Self-managed care, including self-sampling for STIs/BBVs, is increasingly commonplace, requiring agency and health literacy. To inform the development of a partner notification trial, we explored barriers and facilitators to correct use of an STI/BBV self-sampling pack among people with mild learning disabilities.
Methods Using purposive and convenience sampling we conducted four interviews and five gender-specific focus groups with 25 people (13 women, 12 men) with mild learning disabilities (July–August 2018) in Scotland. We balanced deductive and inductive thematic analyses of audio transcripts to explore issues associated with barriers and facilitators to correct use of the pack.
Results All participants found at least one element of the pack challenging or impossible, but welcomed the opportunity to undertake sexual health screening without attending a clinic and welcomed the inclusion of condoms. Reported barriers to correct use included perceived overly complex STI/BBV information and instructions, feeling overwhelmed and the manual dexterity required for blood sampling. Many women struggled interpreting anatomical diagrams depicting vulvovaginal self-swabbing. Facilitators included pre-existing STI/BBV knowledge, familiarity with self-management, good social support and knowing that the service afforded privacy.
Conclusion In the first study to explore the usability of self-sampling packs for STI/BBV in people with learning disabilities, participants found it challenging to use the pack. Limiting information to the minimum required to inform decision-making, ‘easy read’ formats, simple language, large font sizes and simpler diagrams could improve acceptability. However, some people will remain unable to engage with self-sampling at all. To avoid widening health inequalities, face-to-face options should continue to be provided for those unable or unwilling to engage with self-managed care.
- delivery of health care
- health services research
- patient participation
- qualitative research
- sexual health
Data availability statement
Data are available upon reasonable request. The data that support the findings of this study are available from the corresponding author (AM).
This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
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- delivery of health care
- health services research
- patient participation
- qualitative research
- sexual health
Introduction
Healthcare systems worldwide are facing increasing demand.1 2 Recent shifts in healthcare policy and practice are focusing increasingly on self-managed and remote care as a way to address demand and in some cases increase access to care by using digital/online care pathways.3–5 The recent COVID-19 pandemic has accelerated the pace of change.6 Sexual healthcare is at the forefront of self-managed care, and services such as postal self-sampling for STIs/bloodborne virus (BBV) are commonplace7 8 and sometimes the recommended or sole option for asymptomatic people.7
Self-managed care demands agency and health literacy (the ability to seek health information, understand its relevance and enable people to act on that information and make decisions).9 10 Despite increasing use of self-managed care, the views and opinions of people with low health literacy are not known. This is important because some of those at greatest risk of STIs/BBV are from vulnerable groups who have low health literacy and already experience considerable health inequalities, particularly regarding access and uptake of healthcare.11
People with learning disabilities often have low health literacy. This is because a learning disability is a lifelong condition that starts before adulthood and affects development; individuals will need assistance to understand information, learn new things and function independently.12–14 Within the UK there are 1.5 million people with mild to moderate learning disabilities,15 16 26 000 of whom live in Scotland and are known to require support.17 However, there are almost three times as many people with learning disabilities, or who have been recorded as having additional support needs when at school, who do not identify as having learning disabilities in adulthood and importantly do not benefit from learning disability services.13
As part of intervention development, ahead of the LUSTRUM (Limiting Undetected Sexually Transmitted infections to RedUce Morbidity) partner notification randomised controlled trial of accelerated partner therapy (APT),7 we explored the perspectives of people with mild learning disabilities. We aimed to identify potentially modifiable elements of the partner STI/BBV self-sampling packs with the broader aim of increasing access to this type of self-managed care for people with mild learning disabilities and people with low health literacy more broadly.
We aimed to address three research questions:
What challenges do people with mild learning disabilities encounter with self-managed care for STIs and BBV?
What are the views and opinions of people with mild learning disabilities on the self-sampling pack and its contents?
Which elements of the pack could be adjusted to improve uptake and facilitate correct usage?
Methods
Participants
Participants were heterosexual people and men who have sex with men (MSM), with mild learning disabilities, aged 18–65 years and able to communicate in English.
We used existing relationships with community groups and organisations in Central Scotland and personal contacts to inform people with mild learning disabilities about the study. We sent formal letters/emails to our contacts and attended group meetings to discuss the study and answer any questions before recruitment.
Sampling and recruitment
We used purposive and convenience sampling, making efforts to recruit heterosexual people, MSM and people of non-cis genders.
Participant information sheets and consent forms were adjusted to address accessibility needs (online supplemental appendices 1 and 2). The lead researcher (AM) is a registered learning disability nurse. His expertise was used to develop all recruitment materials and other elements of the research processes which needed adapting.
Supplemental material
Supplemental material
We recruited participants through gatekeepers (charitable/voluntary organisations) or directly, depending on the preference of the community group. Where recruitment was via gatekeepers we provided an information sheet which detailed the inclusion criteria and the participant information sheet to enable selective distribution. The inclusion criteria and ability to give informed consent were initially assessed by gatekeepers. Where we sought consent directly from potential participants, we assessed comprehension and understanding of the study information and ability to use this to make an informed decision. We also assessed ability to give informed consent before and throughout the interview/focus group.
Interviews and focus groups took place in community settings in Central Scotland between July and August 2018. Participants were required to dedicate approximately 1 hour to the study and had the option of a support person being present for part or all of the research activities. Participants were compensated with a £30 voucher.
All interviews were audio-recorded using digital devices and were transcribed in a Word document format for the purpose of analysis. Data collected were fully anonymised for reporting, presentation, archiving and/or publication purposes. All data were securely transported, transferred and stored in compliance with relevant data management guidelines.
In total, we conducted four interviews with one male and three female participants, and five focus groups that comprised three all-male groups with a total of 11 participants and two all-female groups with a total of 10 participants (table 1).
Participant characteristics
Procedure
The researchers (AM, GV and RL) conducted the interviews and focus groups using a semistructured topic guide (online supplemental appendix 3). Following introductions, the researcher(s) provided an explanation of the study. Researchers reminded participants that the interview/focus group would be audio-recorded and that they were free to leave at any point, and explained the processes for data handling and ensuring anonymity and confidentiality.
Supplemental material
The researchers checked participants’ understanding of the purpose of the interview or focus group, answered any questions and then sought informed written consent and completed demographic questions.
We began the interview/focus group by showing the participant(s) either the male and female self-sampling/APT packs and discussing how it should be used (figures 1 and 2). We explained that the packs would be provided to people diagnosed in clinics with chlamydia (described as the most common STI) to take to their sex partners. For this to happen, the sex partner would first need to have a telephone consultation with a qualified healthcare professional in clinic. We also explained that we had already conducted extensive pretrial work with diverse groups of people recruited from sexual health clinics and community settings to develop the pack’s contents and instructions.
Visual aid pack (women). The pack contained information about chlamydia, instruction leaflet on how to use the pack, urine collection container (for men) or vulvovaginal swab (for women), blood sample collection kit, return envelope, security seal, red label (advising accuracy of tests depends on following sample taking instructions) and completing the laboratory form, and condoms.
Visual aid pack (men). The pack contained information about chlamydia, instruction leaflet on how to use the pack, urine collection container (for men) or vulvovaginal swab (for women), blood sample collection kit, return envelope, security seal, red label (advising accuracy of tests depends on following sample taking instructions) and completing the laboratory form, and condoms.
Self-sampling packs used in interviews and focus groups
The topic guides were used to elicit barriers and facilitators to using the pack before exploring the testing kit content and how they are used.
We asked participants to open the packs, look at the contents and tell us what they thought of the packs. We then asked participants to read the instructions in the pack, describe the contents of the pack and explain how they would use the contents.
Analysis
We combined focus group and individual interview data. We balanced deductive and inductive thematic analyses of audio transcripts18 to explore issues associated with the barriers and facilitators to correct use of the pack and its contents. Deductive analysis focused a priori on the barriers and facilitators to the correct use of the pack and its contents. In this way, the analysis balanced an inductive understanding of how participants understood the content of the self-sampling pack and its use. First, we conducted an initial sweep of the data enabling us to code in relation to the main elements of the pack, corresponding to the key research questions. Then we conducted a second round of more participant-led, inductive analysis. AM then coded these broad elements of the transcripts to generate participant-led themes. AM and MP reviewed and discussed the themes before defining and naming them. The data generated were stored and organised using NVivo V.11 software.
Results
Six key themes emerged. Table 2 shows representative verbatim quotations illustrating the underlying themes, relating to our three research questions.
Extracts illustrating themes within participants’ accounts
We present a narrative discussion of each theme, drawing out barriers and facilitators to using the pack and its contents.
Accessing sexual healthcare
This theme identified some of the significant challenges that participants experience, particularly when accessing and trying to understand new and complex information.
Participants’ knowledge of STIs was limited and this compounded the challenges of grasping new information. Although the participants all had a mild learning disability, this encompassed a range of cognitive abilities, specific difficulties and literacy skills. Written information was thought to be particularly challenging or inaccessible by all.
Support from others
Many participants explained that decisions about their health and well-being are often undertaken by others and restrictions put on risk-taking behaviours. Some participants continue to live with parents, highlighting this as a particular difficulty for sexual health when privacy was important.
Most participants received some support in their daily lives and often relied on guidance from others when navigating uncertain and unfamiliar areas. This was often with someone they trust and where privacy is respected, which was also the case when faced by a self-sampling pack.
Participants voiced a need for someone else to help navigate the pack, and due to the sensitivity or privacy around sexual health issues this was an additional consideration when asking for help. For some, the complexity of the pack and the knowledge and understanding required to undertake self-sampling meant that they would rather go to their general practitioner (GP) or sexual health service than try themselves.
Using the pack
Most participants described feeling overwhelmed to varying degrees when opening the pack and did not know where to start. This could prevent them from proceeding further.
Most participants found the details included in the chlamydia information sheets (the infection, health consequences, treatment and partner notification) (online supplemental appendix 4) to be too long and difficult to read. They could not relate the information to the actual sampling kits in the pack.
Supplemental material
Despite the challenges voiced by most of the participants, the opportunity to use a self-sampling pack at home was welcomed by some due to convenience. Some also perceived self-sampling less embarrassing than attending a sexual health clinic or GP.
Accessibility of the pack
The inclusion of diagrams and pictures was seen as a welcome step towards an easier-to-read format by all participants. However, participants voiced problems interpreting the diagrams which illustrated the anatomical sites for self-sampling. This was a particular problem for women who had difficulties relating the diagrams to their own anatomy. Written information relating to each of the tests contained in the pack was felt to enhance the usability of the pack.
Participants suggested several improvements to aid clarity and remove ambiguity. These included adopting an ‘easy read’ format,19 avoiding columns of text, and simplifying how the key health messages are presented within the pack to create a more user-friendly feel. Specific suggestions included making it easier to identify items mentioned in the guidance notes with the pack components by numbering them and cross-referencing. For some, an accompanying online ‘YouTube’ video would be welcomed. (Videos were available as part of the wider trials; however, participants taking part in this study were not made aware of them.20)
Contents of the pack
The number of test components in the pack created some anxiety and participants had difficulty understanding their purpose. The perceived lack of a clear process and sequence for undertaking the different activities needed to successfully self-sample was problematic. Interpreting anatomical diagrams depicting sampling sites and diagrams showing what to do with the samples were thought to be particularly challenging.
Condoms contained in the pack were familiar to most participants and were seen as a positive step in preventing future STIs.
Using the contents of the pack
Overall participants found the process daunting and at times confusing. They voiced fears about efficacy, most stating that they would need support to undertake the tests. Obtaining samples was felt to be particularly difficult; most participants felt unclear about what was required, how to take the samples and what to do with them subsequently.
Many women did not seem to have sufficient understanding of their own anatomy and experienced difficulties in interpreting the anatomical diagrams. This led to a lack of confidence in their ability to follow the instructions provided to take a vulvovaginal swab. They also voiced concerns about appropriate technique and the potential for issues with reliability of the test by doing it incorrectly.
The motor skills and manual dexterity required for taking blood samples gave cause for concern and were felt to be a significant barrier to successful self-sampling. However, where participants had previous experience of similar procedures, such as diabetic monitoring, the familiarity gave more confidence.
Discussion
All participants in this study found at least one element of the pack challenging or impossible. Some felt able to manage some of the tasks alone or with help from someone trusted, but others expressed bewilderment and a lack of ability to engage with the pack. However, many welcomed the opportunity to undertake sexual health screening without attending a sexual health clinic, and the inclusion of condoms in the pack was regarded as a positive STI prevention message.
Blood sampling and interpretation of female self-swabbing instructions appeared particularly difficult. Reduced manual dexterity, low knowledge of genital anatomy and overly complex instructions and diagrams contributed to the problems described. Adjustments to the pack structure and contents might increase accessibility, including limiting text to only the minimum required for completing self-samples, ‘easy read’ formats, simple language, large font sizes and simpler diagrams of anatomy and how to take samples.
To our knowledge, this is the first study to explore barriers and facilitators to use of an STI/BBV self-sampling pack in people with learning disabilities. As sexual ill health disproportionately affects those with limited agency, low literacy and low health literacy, these findings increase our understanding of the challenges of self-managed care in this vulnerable group and suggest how problems might be overcome.
There are several limitations. Our sample was restricted to people from one area of Scotland and is unlikely to represent the full range of learning disabilities people experience. Most self-managed sexual healthcare requires initial digital engagement, such as ordering a pack online, whereas our study focused ‘downstream’ on the pack itself. In reality, it is likely that some people would not have managed to take even the first step of ordering online and therefore effectively excluded from self-managed care pathways altogether. We had already extensively optimised the packs by simplifying their components in the context of pretrial development work for a partner notification randomised controlled trial.7 Self-sampling packs in contemporary use may not have been developed with this focus on usability. As such, our findings may somewhat overestimate acceptability and feasibility of this type of care for people with mild learning disabilities.
Evidence suggests that uptake of online postal self-sampling is greater in people from more affluent areas,21 which may be viewed as a proxy for health literacy level. It is perhaps unsurprising that people with mild learning disabilities perceived considerable barriers. Evaluations of existing online self-sampling services report sample return rates of 54%–72.5% and blood samples are the least likely to be returned.22 23 Blood sampling was felt to be particularly challenging for our participants, partly due to difficulties with manual dexterity often coexisting with learning disabilities. Participants with prior experience of diabetic monitoring perceived fewer barriers, which suggests that opportunities to learn how to collect blood samples might encourage engagement.
A previous qualitative study of young people’s perceptions of smartphone-enabled self-testing and online care for STIs suggested that some participants were concerned about the accuracy of self-testing.21 Similar views were expressed in this study, but concerns related to the participants’ perceived ability to take appropriate samples rather than the accuracy of the test itself.
Although the development of the packs was informed by extensive qualitative research with the intention of creating a simple-to-use pack and to fit the financial constraints of the trial, it was not accessible to most of our participants. This suggests that people with even mild learning disabilities and people with low literacy will need highly tailored self-sampling packs to enable engagement with this type of self-managed care.
‘Easy read’ formats,19 specific layouts, reduction and simplification of information to the minimum, avoiding ambiguity and having a step-by-step guide, with a clear start and end point for sequencing of tests, and ensuring kit components are clearly matched to the accompanying instructions could facilitate pack use. An accompanying video clip could be helpful, but this would need to accurately reflect the exact pack the person is using to avoid further confusion.
Even if adjusted packs are provided, there will be considerable challenges in identifying who would benefit from them, as many people with mild learning disabilities and people with poor health literacy are not known to sexual health services. People from these groups may be more likely to take inadequate samples or sample incorrectly, which may lead to false negative results due to poor technique rather than true absence of infection.
As sexual healthcare becomes increasingly self-managed, we risk excluding vulnerable individuals because they are unable or unwilling to engage with processes which require sophisticated levels of health and digital literacy.13 Education and training for healthcare professionals to assist identification of those individuals is likely to help, but an ‘online first’ approach24 may exclude people with mild learning disabilities from engaging with care at all. Easily accessible alternatives (face-to-face options) are essential to avoid widening health inequalities further.
Although we focused on self-sampling packs for STIs and BBV, our findings will have broad generalisability to other areas of healthcare. These findings may also be of use with people from a broad range of ethnicities, people who speak English as a second language or who do not speak English.
Sexual health services have been at the forefront of self-managed care, but little attention has been given to the needs of those who are not health and digitally literate. Future work needs to quantify and characterise people with sexual health needs and risks who choose not to or are unable to engage with self-managed care. To avoid amplifying health inequalities further, we must develop ways of identifying people who may need additional support in a timely and sensitive way and develop accessible alternative models of care.
Key messages
People with mild learning disabilities found the existing self-sampling pack overly complex; many would not use it and did not feel able to engage with self-managed care at all.
Minimum ‘need to know’ information, very simple diagrams and ‘easy read’ formats specific to the needs of people with mild learning disabilities could improve acceptability.
Adoption of self-sampling and other elements of self-managed care without provision of alternative care models could widen health inequalities.
Face-to-face options need to be provided, but identifying those with limited health literacy will be challenging.
Data availability statement
Data are available upon reasonable request. The data that support the findings of this study are available from the corresponding author (AM).
Ethics statements
Ethics approval
Ethical approval was obtained from Glasgow Caledonian University School of Health and Life Sciences Ethics Committee (HLS/PSWAHS/17/194).
Acknowledgments
We would like to thank all the participants who took part in focus groups and interviews and all individuals and organisations who helped with recruitment for this study. This study has been shaped through ongoing discussion and support from the LUSTRUM team (Claudia S Estcourt (principal investigator), Alex Comer, Alison R Howarth, Andrew Copas, Anna Tostevin, Anne M Johnson, Catherine H Mercer, Chidubem (Duby) Ogwulu, Christian Althaus, Fiona Mapp, Gabriele Vojt, Jackie Cassell, Jean McQueen, John Saunders, Karen Pickering, Maria Pothoulaki, Melvina Woode Owusu, Merle Symonds, Nicola Low, Oliver Stirrup, Paul Flowers, Rak Nandwani, Sarah Lasoye, Sonali Wayal, Susannah Brice, Tracy Roberts) and the Programme Steering Committee (PSC) (Simon Barton (chair), Alex Miners, Artemis Koukounari, David Crundwell, Emmanuel Rollings-Kamara, Lynis Lewis, Rebecca Turner, Robbie Currie, Rachel Shaw, Saima Saddiqui (on behalf of the NIHR programme management)).
Supplementary materials
Supplementary Data
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Footnotes
Handling editor Alec Miners
Deceased Rebecca Laidlaw deceased on 6 October 2019
Contributors AM: study design, data collection, data analysis, interpretation, preparation of manuscript. MP: study protocol and design, data analysis, interpretation, preparation of manuscript. MW-O: study protocol and design, interpretation, preparation of manuscript. PF: conceived the study, study protocol and design, data analysis and interpretation, preparation of manuscript. FM: study protocol and design, interpretation, preparation of manuscript. GV: study protocol and design, data collection, interpretation, preparation of manuscript. RL: data collection, data analysis, interpretation of findings. CSE: study protocol and design, data interpretation, preparation of manuscript. All authors (with the exception of RL, deceased) have reviewed and approved the final manuscript submitted.
Funding This work presents independent research funded by the National Institute for Health Research (NIHR) under its Programme Grants for Applied Research (reference number RP-PG-0614-20009).
Disclaimer The views expressed are those of the author(s) and not necessarily those of the NIHR or the Department of Health and Social Care. The funders had no role in study design, collection, management, analysis and interpretation of data, writing of the report and the decision to submit the report for publication.
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.