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How can we make self-sampling packs for sexually transmitted infections and bloodborne viruses more inclusive? A qualitative study with people with mild learning disabilities and low health literacy

How can we make self-sampling packs for sexually transmitted infections and bloodborne viruses more inclusive? A qualitative study with people with mild learning disabilities and low health literacy
How can we make self-sampling packs for sexually transmitted infections and bloodborne viruses more inclusive? A qualitative study with people with mild learning disabilities and low health literacy

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
1368-4973
276-281
Middleton, Alan
6f16cb26-da00-43c0-b383-31754e28f441
Pothoulaki, Maria
d7d396fd-0f21-4fbd-b2c1-466128f45fb6
Woode Owusu, Melvina
e323ba6e-6e71-4e3d-ac3b-6b7903e8f7bb
Flowers, Paul
552c5fd7-75dc-479f-b2e3-d66bbaad4b3f
Mapp, Fiona
bb6e3fef-fc51-4b9d-8708-13635f6f9860
Vojt, Gabriele
20a2722e-e8b5-49e9-9f9f-01cf4e1b1387
Laidlaw, Rebecca
78a4aee7-c349-41de-9056-c69ecc343d34
Estcourt, Claudia S.
1a9c3c9b-5aa4-4a6b-9bc3-ebcc5379718e
Middleton, Alan
6f16cb26-da00-43c0-b383-31754e28f441
Pothoulaki, Maria
d7d396fd-0f21-4fbd-b2c1-466128f45fb6
Woode Owusu, Melvina
e323ba6e-6e71-4e3d-ac3b-6b7903e8f7bb
Flowers, Paul
552c5fd7-75dc-479f-b2e3-d66bbaad4b3f
Mapp, Fiona
bb6e3fef-fc51-4b9d-8708-13635f6f9860
Vojt, Gabriele
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Laidlaw, Rebecca
78a4aee7-c349-41de-9056-c69ecc343d34
Estcourt, Claudia S.
1a9c3c9b-5aa4-4a6b-9bc3-ebcc5379718e

Middleton, Alan, Pothoulaki, Maria, Woode Owusu, Melvina, Flowers, Paul, Mapp, Fiona, Vojt, Gabriele, Laidlaw, Rebecca and Estcourt, Claudia S. (2021) How can we make self-sampling packs for sexually transmitted infections and bloodborne viruses more inclusive? A qualitative study with people with mild learning disabilities and low health literacy. Sexually Transmitted Infections, 97 (4), 276-281. (doi:10.1136/sextrans-2020-054869).

Record type: Article

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.

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More information

Published date: 1 June 2021
Additional Information: Publisher Copyright: © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ.
Keywords: Delivery of health care, Health services research, Patient participation, Qualitative research, Sexual health

Identifiers

Local EPrints ID: 502391
URI: http://eprints.soton.ac.uk/id/eprint/502391
ISSN: 1368-4973
PURE UUID: 9d21927e-cdd0-4d4a-aa73-66a8163c50e1
ORCID for Gabriele Vojt: ORCID iD orcid.org/0000-0002-9135-0684

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Date deposited: 24 Jun 2025 16:55
Last modified: 25 Jun 2025 02:14

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Contributors

Author: Alan Middleton
Author: Maria Pothoulaki
Author: Melvina Woode Owusu
Author: Paul Flowers
Author: Fiona Mapp
Author: Gabriele Vojt ORCID iD
Author: Rebecca Laidlaw
Author: Claudia S. Estcourt

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