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Not yet recruiting NCT07144540

The Effectiveness of NeuroBot in Alleviating Anxiety of Patients Undergoing Neurovascular Surgeries

No phase Interventional Anxiety Patient Compliance Knowledge

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: NeuroBot, Standard Care (in control arm).
Who it may be relevant to
Registry conditions: Anxiety, Patient Compliance, Knowledge. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Hong Kong
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The goal of this randomized controlled trial is to investigate the effectiveness of NeuroBot in alleviating anxiety of patients undergoing neurovascular procedures. The main questions it aims to answer are: Is NeuroBot effective in alleviating anxiety? Is NeuroBot effective in enhancing patients' procedure and disease-related knowledge? Is NeuroBot effective in enhancing patients' compliance to treatment? If there is a comparison group: Researchers will compare with standard perioperative education (control group) to see if there is any difference in results. Participants will be invited to chat with the artificial intelligence based chatbot "NeuroBot" for 6 weeks, from the date of preoperative clinic visit till 4 weeks after the surgery. The participants are allowed to access the NeuroBot at anytime anywhere, to ask surgery- related questions at their discretion.

Detailed description

The NeuroBot is co-developed by the neurosurgeons, nuerosurgical specialty nurses in Queen Elisabeth Hospital and AI experts from the Hong Kong Polytechnic University and the Chinese University of Hong Kong. The NeuroBot is developed based on the large language model that used machine learning algorithm and generative pretrained transformer model. Vast dataset of neurovascular surgery related information from validated sources, including DynaMed, UpToDate and textbooks were included and used for training of NeuroBot. The precision of the responses generated by NeuroBot was verified by a group of neurosurgical domain experts (neurosurgeons and experienced neurosurgical nurses).

Interventions

  • Other NeuroBot
    NeuroBot is an artificial intelligence online accessible chatbot that used machine learning and generative pretrained transformer model for supporting patients undergoing neurovascular surgery during perioperative period
  • Other Standard Care (in control arm)
    Standard care include face-to-face consultation in preoperative nurse clinic and provision of leaflet

Primary outcome measures

  • Anxiety [Time frame: From preoperative (at nurse clinic) to postoperative from 1 week to 4 weeks after surgery]
Secondary outcome measures (4)
  • Knowledge [Time frame: From preoperative nurse clinic visit to 1 week postoperative]
  • Compliance [Time frame: 4 weeks after surgery]
  • Readmission [Time frame: 4 weeks after surgery]
  • Postoperative complications [Time frame: 4 weeks after surgery]

Eligibility criteria

Inclusion criteria

  • aged above 18 years;
  • scheduled for elective neuroendovascular surgery;
  • able to understand Chinese and read Chinese;
  • mobile device with internet capability.

Exclusion criteria

  • identified cognitive impairment or have difficulty in understanding study procedures, following instructions, or providing informed consent;
  • prior exposure to health chatbot to acquire health-related information in previous 3 months;
  • have neurovascular surgeries before

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Triple blind
Primary purpose
Supportive care

Study locations

Hong Kong · 2 centers
  • The Chinese University of Hong Kong — Hong Kong
  • The Chinese University of Hong Kong — Hong Kong

Identifiers

NCT: NCT07144540 · NeuroBot202527

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗