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Active, not recruitingNCT06038669Updated Mar 27, 2026

User Evaluation of a Home-collection Kit for People With Diabetes

An observational study in Diabetes, sponsored by University Hospitals of North Midlands NHS Trust. Active, not recruiting at 1 site in United Kingdom. Open to participants aged 18 Years to 90 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-03-27.

Sponsored by University Hospitals of North Midlands NHS Trust · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
63
Ages
18 Years to 90 Years
Sex
All
01

Study summary

Type 1 and Type 2 are the most common types of diabetes mellitus. Although the cause of Type 1 is different to Type 2, they can both lead to high blood glucose levels as the patient is unable to store and use sugar. The disease is an epidemic of the 21st century which is increasing, having a current prevalence of approximately 8%.

Poor disease control is associated with a range of long-term health conditions which have a severe impact upon quality of life and are responsible for the increased morbidity and mortality associated with the disease.

Healthcare professionals use HbA1c as the main marker to monitor diabetic control. Patients with diabetes have regular review appointments to monitor their overall health and discuss their HbA1c target and results. The purpose of monitoring patients with diabetes is to improve patient outcomes. It is known that poor control is associated with poor clinical outcomes and also that reduced monitoring is linked to suboptimal diabetic control. Therefore, aiming for the correct monitoring frequency helps towards achieving the best control which can lead to the most favourable clinical outcomes. The inconvenience of attending for a blood test and follow-up appointment is a major factor affecting patient adherence to monitoring, locally approximately 50% of patients with diabetes have their HbA1c level measured either too soon or too late.

To address this issue and improve access to monitoring at the correct time interval we aim to produce a HbA1c home testing kit which can be posted back to the laboratory at the convenience of the patient. The kit will be developed based on feedback from patients with diabetes and will use a dried blood spot sample to produce HbA1c results comparable to the whole blood standard method.

02

Conditions studied

  • Diabetes

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03

In context

Diabetes Mellitus

10,925 studies on the registry are indexed under Diabetes Mellitus; 1,319 are open to participants now.

This study's enrollment of 63 is below the median of 233 across 2,220 observational studies indexed under Diabetes Mellitus.

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Lead sponsor

University Hospitals of North Midlands NHS Trust is the lead sponsor of 28 studies on the registry; 9 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Diabetic patients (type I and II) aged over 18 years old.

Healthcare professionals aged 18 or over who work with patients with diabetes.

Inclusion criteria

  • Diagnosis of Type I or Type II diabetes
  • Aged 18 years or over
  • Venous blood sample for HbA1c collected within the two weeks prior to the clinic appointment
  • Ability to provide fully informed consent

Exclusion criteria

Exclusion Criteria:

  • Non-English speaking where translation of the study documents and procedures could limit fully informed consent
  • Severe visual impairment which would leave the participant unable to complete the study procedures.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
63 participants (actual)
Patient registry
No

Groups and cohorts

  • People with diabetes

    Patients who have diabetes will be asked to use a home collection kit to collect a dried blood spot sample which will be compared to the HbA1C result.

    Device: Dried blood spot device

  • Health care professionals

    Health care professionals who work with diabetic patients will be interviewed and asked about diabetes monitoring in the healthcare setting, comments on current laboratory service, patient engagement, comments on service improvement

    Other: Healthcare professional interviews

Interventions

  • DeviceDried blood spot device

    Patients will be asked to provide a dried blood spot sample

  • OtherHealthcare professional interviews

    Health care professionals only will be interviewed using the topic guide and asked about their experience of diabetes monitoring

06

What researchers measure

Primary outcomes

  1. DBS kit assay performance

    For the DBS-based home collection kit used by patients to be 'fit for purpose', it must achieve the following: Assay performance - correlation and bias. Correlation coefficient (r2 value) from linear regression plot should be \>0.95 with a bias of less than 5%.

    Time frame: 1 year, 3 months

Secondary outcomes

  1. Participant questionnaires theme analysis

    Completed participant questionnaires will be collated and analysed for themes. We aim to determine whether participants deem the home-collection kit to be acceptable. The information gained will be used to design a full study.

    Time frame: 1 year, 3 months

  2. Interviews

    The health care professional interview transcripts will be recorded and analysed. The emerging themes will be taken into consideration when designing the full study.

    Time frame: 1 year, 3 months

07

Study locations

1 site
  • University Hospitals of North Midlands NHS Trust
    Stoke-on-Trent, United Kingdom
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06038669
Lead sponsor
University Hospitals of North Midlands NHS Trust
Responsible party
Sponsor
First posted
Sep 15, 2023
Start date
Feb 20, 2024
Primary completion
Mar 31, 2025
Completion
Dec 31, 2026 (estimated)
Last update
Mar 27, 2026

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

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