Postoperative Follow-up Via Artificial Intelligence-Based Application Versus Automated Messaging Application in Patients Receiving Continuous Regional Analgesia: A Comparative Study
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 166
- 试验地点
- 1
- 主要终点
- Comparison of patient-initiated inquiry rates between AI-App and Control-App
研究概览
简要总结
Effective postoperative analgesia is critical for patient recovery, satisfaction, and the reduction of hospital stay duration. Continuous peripheral nerve blocks (CPNB) via catheter placement represent a cornerstone in achieving these objectives. Traditionally, follow-up for these patients has relied on standardized telephone protocols conducted by trained personnel. Original previous research in 2024 demonstrated that an automated text-messaging platform was feasible and maintained high patient satisfaction, it resulted in a significantly higher rate of unscheduled patient-initiated inquiries (28.3% vs. 6.4%) compared to traditional phone calls, likely due to a lack of adaptive response capabilities.
Objective: This study aims to evaluate an enhanced technological iteration of our follow-up platform. By integrating an Artificial Intelligence (AI) interface trained on specialized clinical protocols, the new system is designed to provide automated, personalized and adaptive recommendations to patients.
Methods and Intervention: The study will compare the effectiveness of this AI-driven platform against the previous version of the non-adaptive automated messaging system. The primary outcome is to compare the number of patient-initiated inquiries (re-consultations). Secondary outcomes include patient satisfaction, adherence to the follow-up protocol, and response rates from postoperative days one through three.
Impact: The investigators hypothesize that the integration of AI will optimize human resources and improve patient autonomy without compromising safety or satisfaction, ultimately providing a scalable model for postoperative regional analgesia monitoring.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Health Services Research
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 75 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Patients aged between 18 and 75 years.
- •Physical status classification ASA I or II.
- •Scheduled for ambulatory surgical programs at UC Christus Health Network centers (Hospital Clínico, Clínica San Carlos de Apoquindo, or Centro Médico Santa Lucía).
- •Patients receiving postoperative pain management via continuous peripheral nerve block (CPNB) with a perineural catheter and disposable infusion pump.
- •Ownership and documented proficiency in operating a smartphone to access the mobile application.
- •Provision of written informed consent.
排除标准
- •Inability to understand or follow the digital monitoring protocol.
- •Patients not meeting the age or ASA physical status requirements.
研究组 & 干预措施
AI-App
Artificial Intelligence-driven application
干预措施: AI-driven follow-up platform (Other)
AI-App
Artificial Intelligence-driven application
干预措施: Satisfaction (Other)
AI-App
Artificial Intelligence-driven application
干预措施: Adherence to the follow-up protocol (Other)
AI-App
Artificial Intelligence-driven application
干预措施: Response rates from postoperative days one through three (Other)
Control-App
Standard automated messaging application
干预措施: Satisfaction (Other)
Control-App
Standard automated messaging application
干预措施: Adherence to the follow-up protocol (Other)
Control-App
Standard automated messaging application
干预措施: Response rates from postoperative days one through three (Other)
结局指标
主要结局
Comparison of patient-initiated inquiry rates between AI-App and Control-App
时间窗: From registration to the end of the 3-day outpatient postoperative follow-up
Comparison of patient-initiated inquiry rates between the Artificial Intelligence-driven application (AI-App) and the standard automated messaging application (Control-App) during ambulatory postoperative follow-up.
次要结局
- Engage with the AI-driven app(From registration to the end of the 3-day outpatient postoperative follow-up)
- Assessment patient satisfaction(From registration to the end of the 3-day outpatient postoperative follow-up)
- Adherence between the Control-App and AI-App(From registration to the end of the 3-day outpatient postoperative follow-up)
