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
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Switzerland
University Hospital Basel
RECRUITING
Basel
Contact Information
Primary
Zeljko Djakovic, MD
zeljko.djakovic@usb.ch
+41 61 328 51 96
Time Frame
Start Date: 2025-07-30
Estimated Completion Date: 2026-06
Participants
Target number of participants: 200
Treatments
Experimental: digital follow-up
digital follow-up by questionnaire in addition to routine follow-up
Active_comparator: standard follow-up
routine follow-up
Related Therapeutic Areas
Sponsors
Leads: University Hospital, Basel, Switzerland

This content was sourced from clinicaltrials.gov