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NCT Number: NCT07044440

Digital Follow-up Program After Discharge Home Following Thoracic Surgery

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital Basel

Basel, 4031, Switzerland

Location status: Recruiting

Location contact

Zeljko Djakovic, MD

CONTACT

[email protected]

+41 61 328 51 96

Zeljko Djakovic, MD

PRINCIPAL_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

digital outpatient follow-up

Other

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

standard follow-up

Other

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

Primary outcomes

  1. Subjective pain perception

    Time frame: 4 weeks after discharge home

    Impact on the subjective pain perception is assessed by the numeric rating scale (NRS). Scale ranges from 0-10 while 10 indicates more pain

Secondary outcomes

  1. General well-being

    Time frame: 4 weeks after discharge home

    General well-being is assessed by the numeric rating scale (NRS). Scale ranges from 0-10 while 10 indicates better outcome

  2. Post-Discharge documentation of analgesic use

    Time frame: During the 4 weeks after discharge home

    Assessment of any analgesics admitted after discharge home

  3. Emergency consultations

    Time frame: During the 4 weeks after discharge home

    Number of emergency consultations within 4 weeks after discharge home

  4. Readmissions

    Time frame: During the 4 weeks after discharge home

  5. postoperative complications

    Time frame: During the 4 weeks after discharge home

    postoperative complications after hospital discharge home according to the Clavien-Dindo Classification of surgical complications

Study contacts

Contact information is provided by the study sponsor or research team.

Zeljko Djakovic, MD

CONTACT

[email protected]

+41 61 328 51 96

Sponsors and collaborators

Lead sponsor

University Hospital, Basel, Switzerland

Other

Registry information

Official study title

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

Acronym: DFP

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jul 1, 2025
Registry last updated
Aug 5, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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