Skip to content

Verification and Promotion of the Comprehensive-Cycle Dynamic Intervention and Precision Management System for Diabetes Mellitus

Verification and Promotion of the Comprehensive-Cycle Dynamic Intervention and Precision Management System for Diabetes Mellitus

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114620
Enrollment
Unknown
Registered
2025-12-15
Start date
2025-12-17
Completion date
Unknown
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 diabetes and prediabetes

Interventions

X Life – Smartphone:During this phase, participants utilised the X Life system via their smartphones to complete dietary logging, information viewing, and system prompt-related operations within real-
X Life – AR Glasses:Participants will use the X Life system while wearing augmented reality (AR) glasses. In daily life settings, the system presents diet-, physical activity-, and glucose-related inf
SIBIONICS App:Participants will use the commercially available digital health application, the SIBIONICS app, to record glucose- and lifestyle-related information and view basic data visualisations. T

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18–70 years; 2. Diagnosed with type 2 diabetes mellitus or impaired glucose tolerance; 3. Able to understand the study procedures and independently use smart terminal devices; 4. Willing to wear a continuous glucose monitoring (CGM) device and complete the required assessments; 5. Provided written informed consent.

Exclusion criteria

Exclusion criteria: 1. Significant visual or vestibular system impairment; 2. A history of moderate or severe motion sickness; 3. Ocular or head/skin conditions that may interfere with wearing AR glasses; 4. Cognitive impairment; 5. Participation in a similar wearable-device study within the past three months; 6. Other medical or psychological conditions deemed by the investigator to make participation unsuitable.

Design outcomes

Primary

MeasureTime frame
System Usability Scale (SUS) score;System-recorded usage metrics;

Secondary

MeasureTime frame
Single Ease Question (SEQ) score;Net Promoter Score (NPS);Simulator Sickness Questionnaire (SSQ) score;Diabetes Distress Scale (DDS) score;Hypoglycaemia Fear Survey (HFS) score;Usage scenario preference;Open-ended user feedback;

Countries

China

Contacts

Public ContactHuating Li

Shanghai Sixth People's Hospital

huarting99@sjtu.edu.cn+86 139 1650 2465

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026