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A Randomized Controlled Trial of AI Smart Glasses-Based First-Person Real-Time Video with Remote Voice Guidance versus Traditional Bedside Teaching for Clinical Skills Training in Medical Students

A Randomized Controlled Trial of AI Smart Glasses-Based First-Person Real-Time Video with Remote Voice Guidance versus Traditional Bedside Teaching for Clinical Skills Training in Medical Students

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124482
Enrollment
Unknown
Registered
2026-05-13
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

None listed

Interventions

AI glasses remote voice guidance group:The teaching physician, relying on real-time images, communicates with the research subjects through voice, providing explanations of operation steps, reminders
Traditional bedside teaching group:The teaching physician adopted the conventional clinical teaching method, providing face-to-face guidance to the research subjects through oral explanations, manual

Sponsors

Shenzhen University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: 1.Age range: 18-30 years old. Clinical medicine undergraduate interns or professional master's trainee physicians; 2.Have not systematically learned or mastered the target clinical operations set in this trial (confirmed through pre-test scoring, with the operation pass rate being less than 60%); 3.Normal vision and hearing, without contraindications for wearing smart glasses (such as severe refractive errors not corrected, eye diseases, etc.), and able to operate smart devices proficiently; 4.Voluntarily sign the informed consent form and willing to cooperate in completing the entire trial process and follow-up; 5.During the trial, there are no situations of long-term absence or leave, which can ensure full participation.

Exclusion criteria

Exclusion criteria: 1.Those who have mastered the target clinical operation (with a pre-test pass rate of >= 60%) or have relevant operational experience; 2.Those with visual or auditory impairments who cannot wear the AI glasses properly or receive voice guidance; 3.Those with mental disorders, severe physical diseases, or cognitive functional impairments who cannot cooperate in completing the operation and assessment; 4.Those who cannot complete the intervention or follow-up during the trial due to personal reasons, or who refuse to cooperate with data collection; 5.Those who are currently participating in other similar clinical teaching trials.

Design outcomes

Primary

MeasureTime frame
Total operation duration;Compliance and accuracy rate of key operation steps;

Secondary

MeasureTime frame
Re-test qualification rate after 1 week;Cognitive load;

Countries

China

Contacts

Public ContactXiaoyong Chen

Shenzhen University General Hospital

1255005341@qq.com+86 755 2183 9100

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026