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Search / Trial NCT07055139

Digital Aftercare for Wrist and Clavicle Fractures

Launched by LUZERNER KANTONSSPITAL · Jun 27, 2025

Trial Information

Current as of July 24, 2025

Not yet recruiting

Keywords

Distal Radius Fracture Clavicle Fracture Digital Aftercare App Based Aftercare App Based Rehabilitation Wrist Fracture Fracture Recovery Functional Outcome Quick Dash Prwe E Health Patient Satisfaction Quality Of Life Eq 5 D Complication Rate Postoperative Care

ClinConnect Summary

This clinical trial is studying a new way to care for adults after surgery for certain broken bones in the wrist or collarbone. Instead of the usual in-person check-ups, this study will compare traditional follow-up visits with a digital aftercare program that patients can access through a smartphone app. The main goal is to see how well patients recover function in their wrist or shoulder three months after surgery. The study will also look at other important factors like how well the joint moves, how satisfied patients are with their care, their overall quality of life, any complications, healthcare costs, and time off work. For those using the app, researchers will check how easy it is to use and whether patients stick with the program.

Adults between 18 and 65 years old who have had surgery for a straightforward wrist or collarbone fracture may be eligible, as long as they can use a smartphone and understand German to complete questionnaires. People with more complex injuries, those who cannot use a smartphone, or who have certain health or language challenges won’t be able to join. Participants can expect to be followed for at least three months after their surgery, either through regular doctor visits or by using the digital program, to help track their recovery and share their experiences. This study hopes to find out if digital aftercare can be just as effective and convenient as traditional care, potentially making recovery easier and more accessible for patients.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Age between 18 and 65 years
  • Surgically treated, uncomplicated distal radius or clavicle fracture
  • Use of a smartphone (iOS or Android)
  • Ability to understand German and complete study-related questionnaires
  • Provided written informed consent
  • Exclusion Criteria:
  • Polytrauma or additional injuries to the same upper extremity
  • No access to or inability to use a smartphone
  • Cognitive, psychiatric, or language barriers impairing participation
  • Pregnancy
  • Inability or unwillingness to comply with the study protocol

About Luzerner Kantonsspital

Luzerner Kantonsspital (LUKS) is a leading academic hospital located in Lucerne, Switzerland, dedicated to providing high-quality healthcare and advancing medical research. As a prominent clinical trial sponsor, LUKS is committed to fostering innovation in medical treatments and therapies through rigorous clinical studies. The institution emphasizes collaboration with multidisciplinary teams of healthcare professionals, researchers, and academic partners to ensure that its trials adhere to the highest ethical standards and regulatory requirements. With a focus on improving patient outcomes, LUKS leverages its state-of-the-art facilities and expertise to contribute significantly to the advancement of medical science.

Locations

Lucerne, , Switzerland

Patients applied

0 patients applied

Trial Officials

Frank Beeres, Prof. MD

Principal Investigator

Luzerner Kantonsspital

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported