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Digital Follow-up Program After Discharge Home Following Thoracic Surgery

The Development and Evaluation of a Digital Follow-up Program During the Initial Four Weeks After Discharge Home Following Thoracic Surgery. A Confirmatory, Single-center, Prospective, Non-blinded, Randomized, Controlled Study

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07044440
Acronym
DFP
Enrollment
200
Registered
2025-07-01
Start date
2025-07-30
Completion date
2026-06-30
Last updated
2025-08-05

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

Conditions

Follow-up, Mobile Health, Post Operative Recovery, Thoracic Surgery

Keywords

Electronic Follow-up, Thoracic Surgery

Brief summary

The aim of the study is to evaluate whether a digital follow-up program can improve postoperative pain management and quality of life in patients during the first 28 days after discharge home following thoracic surgery, compared to standard follow-up care.

Detailed description

Thoracic surgery is essential for treating conditions such as thoracic malignancies, trauma, and chronic pulmonary diseases. While often life-saving, recovery after thoracic surgery can be challenging. Enhanced Recovery After Surgery (ERAS) programs have improved outcomes across surgical fields, but their impact on postoperative quality of life (QoL) in thoracic surgery is under-researched. QoL post-surgery involves factors such as pain, physical and respiratory function, psychological well-being, and return to daily life. Effective communication between patients and their physicians post-discharge is crucial for early detection and management of complications. Studies in other surgical areas (e.g., colorectal and cardiac surgery) have shown that mobile apps for follow-up can reduce emergency visits, readmissions, and improve patient experience. However, similar evidence is scarce in thoracic surgery. Existing studies suggest electronic patient-reported outcome (ePRO) systems could help monitor symptoms and improve care, but further research is needed. Despite promising results in other specialties, there is limited evidence on the use of digital tools to monitor and support recovery after thoracic surgery. Given the importance of pain management, QoL, and preventing complications, the researchers aim to explore whether a digital follow-up program could offer measurable benefits for patients recovering at home. The study aims to develop and evaluate a digital follow-up program for patients in the first 28 days after discharge home from thoracic surgery. The primary objective is to assess whether active, digital patient-physician communication can improve postoperative pain outcomes, compared to standard follow-up care.

Interventions

OTHERdigital outpatient follow-up

In addition to routine outpatient follow-up visits on day 14 and 28 post-operative, digital follow-up by questionnaire on their health status and general well-being are provided. Possibility to request an interaction with a doctor from our department at any time during the 28 days following discharge

OTHERstandard follow-up

routine outpatient follow-up visits on day 14 and 28 post-operative

Sponsors

University Hospital, Basel, Switzerland
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients who have signed an informed consent form and underwent a surgery performed at the Thoracic Surgery Department of the University Hospital Basel * Age ≥ 18 years at the time of informed consent * First participation in the Study * Patient operated under general anesthesia * Patients who are in possession of a smart phone or personal computer and have an e-mail account and are able to answer a digital questionnaire. Or an immediate caretaker in the same household owns a smartphone or personal computer and is familiar with the use * Patients who understand verbal and written German or French * Patients discharged at home after surgery * Hospital stay \> 3 nights after surgery

Exclusion criteria

* Patients under preoperative opioid/cortisone therapy * Patients who are unable to follow the procedure of the study, e. g. read or understand German or French, psychological disorders, dementia, etc. * Enrolment of the investigator, his/her family members, employees and other dependent person * Patients with polytrauma or who underwent mediastinoscopy

Design outcomes

Primary

MeasureTime frameDescription
Subjective pain perception4 weeks after discharge homeImpact on the subjective pain perception is assessed by the numeric rating scale (NRS). Scale ranges from 0-10 while 10 indicates more pain

Secondary

MeasureTime frameDescription
General well-being4 weeks after discharge homeGeneral well-being is assessed by the numeric rating scale (NRS). Scale ranges from 0-10 while 10 indicates better outcome
Post-Discharge documentation of analgesic useDuring the 4 weeks after discharge homeAssessment of any analgesics admitted after discharge home
Emergency consultationsDuring the 4 weeks after discharge homeNumber of emergency consultations within 4 weeks after discharge home
ReadmissionsDuring the 4 weeks after discharge home
postoperative complicationsDuring the 4 weeks after discharge homepostoperative complications after hospital discharge home according to the Clavien-Dindo Classification of surgical complications

Countries

Switzerland

Contacts

Primary ContactZeljko Djakovic, MD
zeljko.djakovic@usb.ch+41 61 328 51 96

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026