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Randomized Controlled Trial on the Effectiveness of Human-AI Collaborative Personalized Education for Ambulatory Elderly Patients After Cataract Surgery

Randomized Controlled Trial on the Effectiveness of Human-AI Collaborative Personalized Education for Ambulatory Elderly Patients After Cataract Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117779
Enrollment
Unknown
Registered
2026-01-28
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Cataract

Interventions

Control group:On the day of surgery, patients in the control group received routine verbal health education and ward-based video health education.The follow-up nurse conducted a verbal knowledge asses
Experimental group:On the day of surgery, the designated-nurse in the experimental group generates a personalized draft text of the Safety and Life Guidance After Cataract Surgery and a matching ratio

Sponsors

General hospital of central theater command
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: All patients meeting the cataract-related diagnostic requirements, with the relevant criteria established by WHO; Age >= 60 years; Hospitalization duration not exceeding 24 hours; Education level of primary school or above, possessing a smartphone, and able to independently operate WeChat; Clear consciousness, without severe hearing, cognitive, or mental impairments, capable of normal communication; Voluntarily participating in this study and having signed informed consent.

Exclusion criteria

Exclusion criteria: Patients with severe cardiovascular diseases;Patients with severe diseases of other systems or concurrent infections;Patients with psychiatric disorders or cognitive impairment unable to communicate effectively;Inability to use smartphones or lack of assistance for utilizing audio files;Concurrent participation in other clinical studies.

Design outcomes

Primary

MeasureTime frame
Adherence to scheduled follow-ups;Incidence of medication errors;

Secondary

MeasureTime frame
Rate of patient health knowledge mastery;Evaluation of patient health education;Frequency of repeated consultations for postoperative care issues;Nurses' evaluation of new educational models;

Countries

China

Contacts

Public ContactJuan Yu

General hospital of central theater command

82338619@qq.com+86 189 7116 3520

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026