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Not Yet RecruitingNCT07510425

Artificial Intelligence vs. Automated Messaging for Continuous Regional Analgesia Follow-up

Postoperative Follow-up Via Artificial Intelligence-Based Application Versus Automated Messaging Application in Patients Receiving Continuous Regional Analgesia: A Comparative Study

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
166 (estimated)
Sponsor
Pontificia Universidad Catolica de Chile · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
OTHERAI-driven follow-up platformThe 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.
OTHERSatisfactionRegister patient satisfaction, adherence to the follow-up protocol, and response rates from postoperative days one through three
OTHERAdherence to the follow-up protocolRegister patient satisfaction, adherence to the follow-up protocol, and response rates from postoperative days one through three
OTHERResponse rates from postoperative days one through threeRegister patient satisfaction, adherence to the follow-up protocol, and response rates from postoperative days one through three

Timeline

Start date
2026-04-01
Primary completion
2026-07-01
Completion
2027-07-01
First posted
2026-04-03
Last updated
2026-04-03

Locations

1 site across 1 country: Chile

Source: ClinicalTrials.gov record NCT07510425. Inclusion in this directory is not an endorsement.