Study of a Patient Cohort Following Digestive Surgical Care After the Implementation of a Telemonitoring and Tele-coordination Platform for Medical, Paramedical, and Social Management

NCT07186738 | Not Yet Recruiting

• 1 other identifier: AP_ED_EPOCA
• Study Type: observational
• Target: 250
• Locations: 1 country
• Sites: 1

Brief Summary

Postoperative hospital stays and complications vary widely after digestive surgery. Enhanced Recovery After Surgery (ERAS) protocols have shortened stays and accelerated recovery after elective procedures, but they remain challenging in emergency surgery and among frail or elderly patients. While theoretical discharge after colorectal surgery is possible between postoperative days 2 and 7, average stays in practice are 12-14 days. Bariatric surgery similarly targets discharge on days 2-3, yet typical stays are 8-10 days. Patients successfully managed under ERAS may face higher readmission risk, often due to worsening comorbidities or serious complications. Prolonged hospitalization and readmissions impact patient safety, comfort, and healthcare costs. Daily hospital costs in surgical units range from €350 to €400. Post-acute care facilities can reduce readmissions but often have long waiting periods. To minimize readmission risk, many surgeons prefer in-hospital postoperative monitoring, limiting early discharge. Recent studies show that connected devices and teleconsultation can provide safe and effective postoperative follow-up. Teleconsultation follow-up is feasible for most patients, with satisfaction rates comparable to in-person visits. Remote monitoring of stoma care has been associated with reduced readmissions. Home-based monitoring using connected vital sign devices in high-risk patients reduces readmissions and emergency visits. In colorectal and bariatric surgery, daily remote monitoring after early discharge (24-48 hours) did not increase morbidity or readmission, suggesting that telemonitoring can safely enable earlier discharge while maintaining patient safety. Continuous monitoring is particularly important for high-risk patients due to rapid deterioration from potential complications. EPOCA is a telemonitoring and telecoordination platform providing medical, paramedical, and social follow-up at home. It combines connected devices, a digital platform for data analysis, and a dedicated medical and paramedical team. Services include teleconsultations, home paramedical care, support for families or care facilities, and 24/7 emergency management. EPOCA reassures patients and caregivers, supports primary care and home care teams, and integrates hospital and emergency services. It addresses challenges posed by aging populations, chronic disease prevalence, and increasingly complex patients. By enabling earlier discharge without increasing readmissions, EPOCA offers a holistic solution bridging hospital and home care. It has already demonstrated success in preventing hospitalizations in high-risk elderly patients and is authorized for telemonitoring of chronic conditions including diabetes, respiratory, renal, and cardiac insufficiency. This study aims to evaluate the feasibility of implementing EPOCA over two years in the CHU Nantes digestive surgery unit. It will target patients undergoing elective or urgent colorectal or bariatric surgery who are at risk of prolonged hospitalization or readmission. High-risk scenarios include anticipated early discharge within 24 hours and patients identified as having elevated readmission risk according to predefined criteria

Conditions

Telemonitoring

Keywords

telemonitoring; digestive surgery

Outcome Measures

Primary Outcomes (1)

• To assess the feasibility of implementing the EPOCA discharge program in the digestive surgery department of Nantes University Hospital

  Cumulative duration of re-hospitalization days up to 90 days post-surgery (number of day)

  90 days post surgery

Secondary Outcomes (1)

• Morbidity rate

  90 days

Study Arms (1)

telemonitoring patient after digestive surgery

EPOCA telemonitoring at home for patients following digestive surgery

Device: EPOCA telemonitoring

Interventions

EPOCA telemonitoring DEVICE

EPOCA is a telemonitoring and tele-coordination platform for medical, paramedical, and social care, enabling the follow-up of acute or chronic patients at home-whether after hospital discharge, as an alternative to hospitalization, or for long-term monitoring. The EPOCA solution relies on connected devices, a digital platform for analyzing incoming data, and a team of medical and paramedical professionals for monitoring and coordination. Remote medical monitoring includes teleconsultations, at-home paramedical care, guidance and support for families, nursing homes, or long-term care facilities, and 24/7 management of home emergencies

telemonitoring patient after digestive surgery

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

The project concerns patients undergoing colorectal or bariatric surgery, either emergent or elective, in the digestive surgery department of Nantes University Hospital, who are at high risk of readmission

You may qualify if:

• Male or female patients over 18 years of age.
• Patients undergoing colorectal or bariatric surgery not routinely managed as outpatient procedures at Nantes University Hospital.
• At least one of the following criteria:
• Anticipated early discharge (within 24 hours post-surgery) for procedures not routinely managed as outpatient at the hospital.
• Estimated risk of readmission greater than 6% according to the Tevis et al. nomogram, adapted to the postoperative context in digestive surgery (\>50 points on this score).
• Patients enrolled in a health insurance plan

You may not qualify if:

• Discharge to a rehabilitation center requested by the patient
• Condition routinely managed as an outpatient procedure
• Patient under home hospitalization care
• Suicidal or heteroaggressive risk in a patient living alone at home
• Homeless patients
• Pregnant or breastfeeding women
• Patients under legal guardianship, conservatorship, or judicial protection

Sponsors & Collaborators

• Nantes University Hospital: lead

Study Sites (1)

CHU Nantes

Nantes, 44000, France

Location

Central Study Contacts

Alexandra Poinas, PhD

CONTACT

02 53 48 28 57; alexandra.poinas@chu-nantes.fr

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: MD PhD

Study Record Dates

• First Submitted: September 15, 2025
• First Posted: September 22, 2025
• Study Start: October 1, 2025
• Primary Completion: February 1, 2026
• Study Completion (Estimated): October 1, 2027
• Last Updated: September 22, 2025

Record last verified: 2025-09

Locations

FR (1)