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NCT Number: NCT07718867

Point-of-care Capillary HbA1c Testing for Type 2 Diabetes Screening Among At-risk Individuals in Rural Dali, China

This project aims to compare Point-of-care capillary HbA1c (POC-cHbA1c) testing and fingerstick random blood glucose (RBG) testing in terms of type 2 diabetes detection rate and cost-effectiveness, in order to optimise current screening strategies for rural populations at high risk of diabetes in rural Dali, China, and to improve treatment adherence and self-management among people with diabetes.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

This is a cluster randomised controlled trial conducted in rural Dali, Yunnan, China, to evaluate the effectiveness and cost-effectiveness of point-of-care capillary HbA1c testing (POC-cHbA1c) for screening type 2 diabetes among high-risk individuals. The study will involve six township health centres in rural Dali. The intervention group will receive immediate on-site POC-cHbA1c testing, while the control group will undergo fingerstick RBG testing, with both groups having confirmatory vHbA1c testing for validation. Primary outcome is the detection rates of T2DM, while secondary outcomes include the detection rate of pre-diabetes, sensitivity, specificity, and economic evaluations such as the incremental cost-effectiveness ratio (ICER). The findings are intended to inform optimized screening strategies in rural settings, potentially leading to earlier diagnosis, better treatment adherence, and improved health outcomes in rural populations at high risk of diabetes.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 18 years or above;
  • Permanent residents of Dali City who have lived locally for at least six consecutive months;
  • Registered as rural residents;
  • No known history of diabetes;
  • Meet at least one of the high-risk criteria for T2DM specified in the Chinese Guidelines for the Prevention and Treatment of Diabetes issued by the Chinese Diabetes Society;
  • Able to understand the study information and provide written informed consent.

Exclusion criteria

  • Known history of T2DM or currently receiving glucose-lowering treatment;
  • HbA1c testing with a clear result within the past three months, or completion of standardised diabetes screening within the past six months;
  • Pregnant or breastfeeding at the time of recruitment;
  • Active thyroid disease or other active endocrine disorders at recruitment, such as Cushing's syndrome or acromegaly;
  • Known haemoglobinopathy, severe anaemia, recent acute blood loss, or history of blood transfusion or blood donation within the past three months;
  • Currently receiving treatment that may substantially affect interpretation of HbA1c, such as erythropoietin therapy or recent high-dose iron therapy.

Treatment and study plan

POC-cHbA1c

Diagnostic Test

Research staff will use quality-certified POC HbA1c devices to perform finger-prick capillary HbA1c testing for participants. Testing will be completed on site and results will be provided immediately.

Fingerstick RBG

Diagnostic Test

Research staff will use standardised glucometers and test strips to measure fingerstick random blood glucose. Test results will be provided on site.

Primary outcomes

  1. Detection rate of T2DM

    Time frame: 1 week

Secondary outcomes

  1. Detection rate of pre-diabetes

    Time frame: 1 week

  2. Sensitivity and specificity

    Time frame: 1 week

  3. Number needed to screen

    Time frame: 1 week

  4. Incremental cost-effectiveness ratio

    Time frame: 3 months and 6 months

Other outcomes

  1. Proportion of treatment adherence

    Time frame: 3 months and 6 months

    Treatment adherence will be measured by the Medication Adherence Report Scale - 5 items, MARS-5

  2. Score of diabetes self-management

    Time frame: 3 months and 6 months

    The level of diabetes self-managment will be calculated as a score using the Summary of Diabetes Self-Care Activities - 6 items (SDSCA-6).

  3. Venous HbA1c levels

    Time frame: 3 months and 6 months

  4. Treatment-related adverse event

    Time frame: 3 months and 6 months

    Hypoglycaemia, anxiety and depression, etc.

  5. Level of satisfaction with the screening method

    Time frame: 3 months and 6 months

    The level of satisfaction with the screening method will be evaluated using a 5-point Likert item (very disappointed, disappointed, neutral, satisfied, very satisfied).

Study contacts

Contact information is provided by the study sponsor or research team.

Levon Yongle Zhan, PhD

CONTACT

[email protected]

852-25185656

Sponsors and collaborators

Lead sponsor

The University of Hong Kong

Other

Registry information

Official study title

Effectiveness and Cost-Effectiveness of Point-of-care Capillary HbA1c Testing for Type 2 Diabetes Screening Among At-risk Individuals in Rural Dali, Yunnan, China: A Cluster Randomised Controlled Trial

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jul 22, 2026
Registry last updated
Jul 28, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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