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NCT06985680

Diabetic Patients,Self-Efficacy,Self-Care Behaviors,Artificial Intelligence-Based

Completed NA Last updated 22 May 2025
What this trial tests

NA trial testing LINE@ Diabetes Health Education Chatbot in Diabetic Patients,Self-Care,Artificial Intelligence-Based,Self-Efficacy in 104 participants. Completed in 18 February 2025.

Timeline
1 February 2024
Primary endpoint
1 November 2024
18 February 2025

Quick facts

Lead sponsorChia-Tzu Line
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposesupportive care
Enrollment104
Start date1 February 2024
Primary completion1 November 2024
Estimated completion18 February 2025
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Chia-Tzu Line

Who can join

Adults 18 to 80, any sex, with Diabetic Patients,Self-Care,Artificial Intelligence-Based,Self-Efficacy or Type 2 Diabetes Mellitus (T2DM). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study employed an experimental research design using a randomized controlled trial methodology. Group allocation was performed randomly by generating serial numbers through a computer. Participants were then randomly assigned to either the experimental or control group by placing the serial numbers into opaque envelopes and selecting envelopes in random order as patients arrived for appointments. The experimental group received conventional face-to-face education in addition to participating in the "Diabetes Smart Assistant" Line@ diabetes education robot program. Education was delivered individually in a one-on-one manner. Researchers spent 15 minutes instructing participants on the operation and usage of the Line@ diabetes education robot program, followed by educational content delivery. Educational sessions lasted for 30 minutes on the day of enrollment, and 15 minutes each at the 3rd and 6th months of enrollment, totaling three one-on-one educational sessions. Additionally, participants received telephone consultations for follow-up during the enrollment period. Telephone education sessions were conducted in the first week of enrollment, the second month, and the fourth month, each lasting 10 minutes, totaling three sessions. The control group received routine education and had follow-up visits every three months for one-on-one education. Data collection for both groups occurred at the time of enrollment, and at the 3rd and 6th months of enrollment.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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