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Consultation Optimization Based on Large Language Models: A Randomized Study to Evaluate the Effect of ChatGPT and DeepSeek on Anxiety and Satisfaction in Patients Undergoing Minimally Invasive Spine Surgery

Consultation Optimization Based on Large Language Models: A Randomized Study to Evaluate the Effect of ChatGPT and DeepSeek on Anxiety and Satisfaction in Patients Undergoing Minimally Invasive Spine Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107672
Enrollment
Unknown
Registered
2025-08-15
Start date
2025-08-15
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Cervical disc herniation

Interventions

DeepSeek Advisory Group:The chief surgeon team used DeepSeek to answer patient questions preoperatively and interpret the information based on clinical experience
ChatGPT Advisory Group:The chief surgeon's team used ChatGPT to answer patient questions before surgery and interpret the information based on clinical experience
Control group:The chief surgeon team used DeepSeek to answer patient questions preoperatively and interpret the information based on clinical experience

Sponsors

Affiliated hangzhou first people's hospital, zhejiang university school of medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Clear diagnosis: Meets the diagnostic criteria for CDH in the "Expert Consensus on Surgical Treatment and Perioperative Management of Cervical Spondylosis (2018)", and is diagnosed as cervical disc herniation by clinical manifestations and imaging examination; 2. Meet surgical indications: According to the "Expert Consensus on Surgical Treatment and Perioperative Management of Cervical Spondylosis (2018)", patients with cervical disc herniation have been treated conservatively for >=3 months, or require surgical treatment due to severe pain or muscle weakness due to nerve compression; 3. 18-80 years old (including 18 and 80 years old); 4. Be able to cooperate with the completion of evaluation and treatment; 5. Understand and be willing to participate in this clinical trial and provide signed informed consent.

Exclusion criteria

Exclusion criteria: 1.People with severe mental illness, aphasia and cognitive dysfunction due to various reasons; 2.Those who are unable to cooperate with the assessment and treatment;

Design outcomes

Primary

MeasureTime frame
Hospital Anxiety and Depression Scale score;

Secondary

MeasureTime frame
Preoperative anxiety scoring scale score;Visual analogue scale score;Satisfaction score (Likert scale-5);

Countries

China

Contacts

Public ContactYu Liang

Affiliated hangzhou first people's hospital, zhejiang university school of medicine

yuliang0601@zju.edu.cn+86 571 5600 7674

Outcome results

None listed

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