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BloodTrackR Usability and Concordance Study (BUCS): Evaluating a Smart Home-Based Blood Collection Platform for Remote Monitoring in Rheumatoid Arthritis (BUCS)

2026年6月19日 更新者:University of Ulster

BloodTrackR Usability and Concordance Study (BUCS)

The BloodTrackR Usability and Concordance Study (BUCS) is evaluating a novel home-based blood collection device and companion mobile application for people with rheumatoid arthritis. Participants will use the BloodTrackR device to collect a finger-prick blood sample at home and complete symptom assessments through the app.

The study will assess how easy the device and app are to use, whether participants can successfully collect high-quality blood samples outside of a healthcare setting, and how closely the results compare with standard venous blood samples collected by a phlebotomist. Findings will help determine the potential of BloodTrackR to support remote monitoring and reduce reliance on NHS phlebotomy services.

研究概览

详细说明

Background:

Blood testing is one of the most important tools in healthcare, but the way samples are collected and processed today creates barriers for both patients and the NHS. Most blood tests require a hospital or GP visit for venous blood draw. This can be inconvenient and stressful for patients, particularly those with long-term conditions who need frequent monitoring, and it places additional demand on already stretched NHS staff. In clinical trials, reliance on centralised sample collection and processing slows recruitment and increases costs. Current alternatives, such as dried blood spot (DBS) sampling, have limitations in accuracy due to the "haematocrit effect," which reduces trust in results.

The impact is significant: patients face delays and additional travel, NHS services struggle with capacity, and healthcare costs increase. There is an urgent need for simple, reliable solutions that support blood testing in the community, reduce workforce pressure, and improve patient experience.

BloodTrackR, is a novel blood collection device and companion mobile app developed by the researchers that allows people collect their own blood samples at home. A key focus of BloodTrackR is the measurement of inflammation in rheumatoid arthritis, which is not visible to clinicians outside clinic visits, so that treatment can be adjusted in real time rather than at the next scheduled appointment. This helps identify early signs of disease flares and ensures disease activity is kept under control. Given that chronic inflammatory conditions are frequently associated with multi-morbidity, BloodTrackR could also provide a platform for monitoring co-occurring conditions, such as diabetes or cardiovascular disease, from the same device. This creates opportunities to consolidate patient monitoring, reduce missed opportunities for treatment adjustment, and ensure therapy is as effective as possible across multiple conditions.

This reusable device incorporates a proprietary plasma separation process that produces dried plasma samples, rather than dried blood spots, overcoming limitations of the haematocrit effect. Built-in sample stabilisation, temperature monitoring, and precise time-stamping safeguard sample quality and integrity during transport and storage. The companion mobile app links samples with patient-reported symptoms and medications, creating rich longitudinal datasets that can inform clinical decision-making, support remote monitoring, and trigger earlier intervention.

This research will evaluate BloodTrackR, a novel blood collection device and companion App designed for use at home or in community settings and in addition, to ascertain:

  1. If the participants can reliably use BloodTrackR to collect and stabilise high-quality blood plasma samples outside of a hospital setting
  2. Will this approach reduce the burden on NHS services?

Aim: This study aims to evaluate the reliability, usability, and acceptability of BloodTrackR-a novel at-home blood/collection device and companion mobile app-to determine its capacity to reduce reliance on NHS phlebotomy services and identify measurable outcomes that indicate its potential to alleviate NHS workforce burden.

Objectives:

  • To Assess usability and patient acceptability of the device and app in real-world settings.
  • Evaluate the quality and stability of samples collected and transported from home.
  • Gather feedback from PPI workshops to inform device refinement and adoption.
  • Generate evidence to demonstrate potential workforce and system benefits for the NHS.

Study Design:

The current research is a usability mixed method study and will be conducted in 3 phases:

Methodology:

Recruitment:

Participants n=20 will be recruited via Rheumatoid Arthritis support groups and their charity partners via the group leaders for which our centre has extensive experience working with and who have already provided feedback on early device design. In addition, participants who have previously taken part in research studies under the CI and have provided enduring consent will also be sent information on the study.

The researcher employed onto the study will arrange to attend the group(s) to give an informal talk about the research and leave Participant information sheets (PIS) for those interested and to answer any questions. If after reading the PIS and the participant is happy to proceed, they will be asked to contact the researcher via the contact details provided on the PIS to check their eligibility via a screening questionnaire. If eligible, the researcher will then gain informed consent either by post or in person prior to participants being enrolled onto the study.

Phase 1: Usability and acceptability: Those participants who have consented to participate in the study will be advised that they will receive their BloodTrackR device by post in a pack complete with instructions. This will be supplemented by remote training on the correct use of the BloodTrackR device and companion app, delivered via Microsoft Teams, to support participants in collecting their own capillary blood sample at home and simultaneously log their assessment of disease activity via the Clinical Disease Activity Index (CDAI) and the Routine Assessment of Patient Index data 3 (RAPID 3) assessment questionnaires which measure the participants physical function, symptoms, pain, and overall global health all via the app. The logged data is accessible only to the named researcher(s) and is de-identified. Usability and compliance will be assessed via a structured questionnaire which will be posted out along with the device to complete when the participant has completed the procedure. In addition, the data usage logged by the App will be collected. This feedback will provide rich insight into user experience, barriers to adoption and opportunities for refinement.

Phase 2: Concordance Study Patient-collected capillary device samples collected via the BloodTrackR device will be validated against matched venous blood draws which will be collected around the same time as they self-collect their device based capillary sample. The participant will be asked to return the device with the sample contained in the well to the Personalised Medicine Centre;PMC in the addressed, prepaid envelope provided. The 6ml venous serum sample will be collected by a qualified phlebotomist to confirm quality and integrity against the device-based samples. The qualified phlebotomist will attend the participant's home solely for the purpose of collecting the venous blood sample. They are not a member of the research team and will have no role in, or influence over, the participant's self-collection of the capillary blood sample using the study device and accompanying app. The phlebotomist's involvement is limited to venepuncture procedures. C-reactive protein (CRP) concentration will be compared between the two sample types using ELISA assays at PMC from the device sample and gold standard hospital laboratory analysis (Altnagelvin hospital, Western Health and Social Care Trust). This will confirm whether CRP values from home-collected plasma samples via the device are equivalent to standard of care phlebotomy, in terms of sample quality and clinical reliability of CRP levels detected. In addition, participants will be asked post procedure to participate in a one-to-one interview either via Teams, telephone or face to face (either in their own home or in C-TRIC). Interviews will be digitally recorded (following informed consent), transcribed verbatim and analysed following the template analysis style outlined by Miles and Huberman (1994).

Phase 3: Health Economic Analysis We will conduct an initial health economic assessment of BloodTrackR relative to current NHS phlebotomy practice. Metrics will include time saved per patient (reduced travel, waiting, and clinic time), reduction in staff workload compared with current phlebotomy practice, and early cost modelling (device/test vs ~£50 per current phlebotomy episode). These analyses will provide early evidence of workforce and system-level benefits.

研究类型

观察性的

注册 (估计的)

20

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

学习地点

      • Londonderry、英国、BT47 6SB
        • 招聘中
        • Personalised Medicine Centre
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

取样方法

非概率样本

研究人群

The study population will consist of approximately 20 adults aged 18 years and older with a confirmed diagnosis of rheumatoid arthritis living in or around Derry/Londonderry, Northern Ireland. Participants must be able to understand written and spoken English and have access to WiFi and a smartphone or tablet. Participants will be recruited through rheumatology patient organisations, support groups, community networks, and research recruitment platforms to evaluate the usability, acceptability, and concordance of the BloodTrackR home blood collection platform.

描述

Inclusion Criteria:

  • Individuals living with rheumatoid arthritis, who attend community groups or rheumatoid arthritis charity groups
  • Aged 18 years or older
  • Able to understand written and spoken English
  • Individuals who have the capacity to consent
  • Access to WiFi and a smartphone/tablet

Exclusion Criteria:

  • Participants <18years
  • Participants taking antibiotics/antivirals
  • No access to WiFi or a smartphone/tablet

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
干预/治疗
Adults with Rheumatoid Arthritis
Adults aged 18 years and older with rheumatoid arthritis who will use the BloodTrackR home blood collection device and companion mobile application. Participants will collect a blood sample at home and undergo paired venous blood sampling for concordance testing. Usability, acceptability, and user experience will be assessed through questionnaires and interviews.
A home-based blood collection device and mobile application that enables remote blood sampling, symptom tracking, temperature monitoring, and sample traceability.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Questionnaire to assess usability of the BloodTrackR Home Blood Collection Platform
大体时间:Immediately after completion of BloodTrackR device use (same day)
Usability of the BloodTrackR device and companion mobile application will be assessed using a study-specific usability questionnaire completed after device use. Participants will indicate whether each step of the blood collection procedure was successfully completed, completed with issues, or not completed, and will provide an overall usability rating on a scale of 0 to 10. Higher scores indicate greater usability and user satisfaction.
Immediately after completion of BloodTrackR device use (same day)

次要结果测量

结果测量
措施说明
大体时间
Post-Procedure Semi-Structured Interview on BloodTrackR User Experience
大体时间:Following completion of device use (up to 1 month)
Participant experience of using the BloodTrackR device and companion mobile application will be explored through a post-procedure semi-structured interview. Interview questions will explore ease of use, acceptability, perceived benefits, barriers to use, and suggestions for improvement. The responses will be summarised descriptively across participants.
Following completion of device use (up to 1 month)
Concordance Between BloodTrackR device and Venous CRP Measurements
大体时间:1 week following device use
Comparison of C-reactive protein (CRP) concentrations obtained from blood samples collected using BloodTrackR and paired venous blood samples analysed using standard laboratory methods.
1 week following device use
Successful Home Blood Sample Collection Rate
大体时间:Up to 1 day following device use
Proportion of participants able to successfully collect and return a blood sample using the BloodTrackR device without assistance.
Up to 1 day following device use
Estimated Patient Time Associated With Blood Collection
大体时间:At completion of study participation (up to 3 months)
A preliminary health economic assessment will compare BloodTrackR with standard NHS phlebotomy pathways. Estimated patient time associated with blood collection, including travel, waiting, and clinic time, comparing BloodTrackR with standard NHS phlebotomy pathways. Findings will be used to inform future economic evaluations of BloodTrackR.
At completion of study participation (up to 3 months)
Estimated Healthcare Staff Workload Associated With Blood Collection
大体时间:At completion of study participation (up to 3 months)
A preliminary health economic assessment will compare BloodTrackR with standard NHS phlebotomy pathways. Estimated healthcare staff workload associated with blood collection procedures comparing BloodTrackR with standard NHS phlebotomy pathways. Findings will be used to inform future economic evaluations of BloodTrackR.
At completion of study participation (up to 3 months)
Estimated Blood Collection Cost per Participant
大体时间:At completion of study participation (up to 3 months)
A preliminary health economic assessment will compare BloodTrackR with standard NHS phlebotomy pathways. Estimated cost per participant for blood collection using BloodTrackR compared with standard NHS phlebotomy pathways. Findings will be used to inform future economic evaluations of BloodTrackR.
At completion of study participation (up to 3 months)

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:David Gibson、Ulster University

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年6月1日

初级完成 (估计的)

2026年9月1日

研究完成 (估计的)

2026年12月1日

研究注册日期

首次提交

2026年6月3日

首先提交符合 QC 标准的

2026年6月15日

首次发布 (实际的)

2026年6月22日

研究记录更新

最后更新发布 (实际的)

2026年6月24日

上次提交的符合 QC 标准的更新

2026年6月19日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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