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Application of LLM-based Conversational AI Agents in Preoperative Anxiety Health Education for Cervi

Application of LLM-based Conversational AI Agents in Preoperative Anxiety Health Education for Cervi

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600131300
Enrollment
Unknown
Registered
2026-08-31
Start date
2026-09-01
Completion date
Unknown
Last updated
2026-09-07

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

Conditions

Preoperative anxiety in patients with cervical spondylosis undergoing elective surgery

Interventions

Intervention group:Routine preoperative health education plus a large language model-based conversational artificial intelligence agent intervention

Sponsors

The Third Affiliated Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18 to 65 years. 2.Single-level C3-C7 cervical spondylotic myelopathy, cervical radiculopathy, or mixed cervical spondylosis caused by degenerative changes, unresponsive to at least 6 weeks of conservative treatment and requiring surgical treatment. 3.Imaging examinations, including CT or MRI, confirm cervical disc herniation or nerve compression, with clinical symptoms and signs consistent with the affected cervical level. 4.Owns a smartphone and is able to perform basic smartphone operations. 5.Voluntarily agrees to participate in the study and provides written informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients undergoing emergency surgery. 2.Patients undergoing revision surgery. 3.Patients with a history of spinal surgery. 4.Patients with a history of psychiatric disorders. 5.Patients receiving long-term psychotropic medication. 6.Patients with severe dysfunction of major organs, including the heart, lungs, liver, or kidneys. 7.Patients considered unsuitable for participation by the investigators for other reasons, such as an expected survival of less than 6 months or severe visual or hearing impairment.

Design outcomes

Primary

MeasureTime frame
State Anxiety Inventory score;

Secondary

MeasureTime frame
Decisional Conflict Scale score;Amsterdam Preoperative Anxiety and Information Scale score;Visual Analogue Scale for Anxiety score;Pittsburgh Sleep Quality Index score;Incidence of adverse events and serious adverse events;

Countries

China

Contacts

Public ContactXuemei Tan

The Third Affiliated Hospital of Southern Medical University

1150788853@qq.com+86 20 62784309

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 19, 2026