About this trial
This prospective, two-arm, open-label clinical trial compares digital aftercare with traditional follow-up in adult patients after surgical treatment of uncomplicated distal radius or clavicle fractures. The primary objective is to assess functional recovery at three months, using the Patient-Rated Wrist Evaluation (PRWE) for wrist fractures and the QuickDASH for clavicle fractures. Secondary outcomes include range of motion, patient satisfaction, quality of life, complication rates, healthcare costs, and work disability. In the digital aftercare group, program adherence and user experience will also be evaluated through app usage data and a structured questionnaire. The study aims to determine whether digital aftercare is a clinically and economically equivalent alternative to standard in-person care.
Eligibility criteria
Qualifiers
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
Disqualifiers
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
Trial design
Treatments tested in this trial
- Digital Aftercare
- Traditional Aftercare
Treatment groups
Sponsors and collaborators
Luzerner Kantonsspital
Lead sponsor
Johnson & Johnson
Collaborator