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Active Not RecruitingNCT07163000

Earlier Diagnosis of Peripheral Neuropathy Using A Simple sCreening Tool (ACT)

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
150 (actual)
Sponsor
Weill Cornell Medical College in Qatar · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is looking at people with diabetes (type 1 and type 2 diabetes) to see how well a short questionnaire, called the ACT, can identify nerve damage in the feet and legs (also known as peripheral neuropathy). The investigators will compare the ACT questionnaire to other commonly used tools (the DN4 and Michigan Neuropathy Screening Instrument) and to an eye-test that detects small nerve fibers in the eye (called corneal confocal microscopy, or CCM). The main goal is to find out if the ACT questionnaire is accurate in detecting nerve damage and painful nerve damage caused by diabetes. The investigators will also look at whether changes in blood sugar levels, measured with a continuous glucose monitor (Freestyle Libre 3 and iCan), are linked to nerve pain and small nerve fiber damage.

Detailed description

This a cross-sectional cohort study in patients with diabetes with the aim of assessing the validity and diagnostic accuracy of the ACT questionnaire in identifying peripheral neuropathy (PN) in patients with diabetes and explore underlying mechanisms for nerve damage. The primary endpoint is to validate the ACT tool in identifying diabetic painful neuropathy against the DN4 questionnaire, Michigan Neuropathy Screening Instrument (MNSI) and in relation to underlying small nerve fibre damage (CCM). And the secondary endpoints include the investigation of the association between glycemic indices using continuous glucose monitoring (CGM- Freestyle Libre 3 and iCan) with neuropathic pain (ACT/DN4/MNSI) and small nerve fibre damage (CCM). Participants will attend 3 visits and the following will be assessed: * Visit 1(baseline): Consent, screening, CCM, ACT, MNSI, DN4, CGM (Freestyle Libre 3). * Visit 2 (14-days follow-up): CGM (freestyle Libre 3), ACT, MNSI, DN4 * Visit 3 (between 1-6 months): CGM (iCan)

Conditions

Timeline

Start date
2025-05-11
Primary completion
2026-12-30
Completion
2026-12-30
First posted
2025-09-09
Last updated
2025-09-09

Locations

1 site across 1 country: Qatar

Source: ClinicalTrials.gov record NCT07163000. Inclusion in this directory is not an endorsement.