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The aim of this study is to investigate the effects of eDialogue versus standard communication pathways on patient-initiated telephone contacts to the hospital following discharge. Secondary aims are to explore the effect on other patient-initiated contacts after hospital discharge (mail, video, SMS, personal attendance) and, if digital team-based communication can positively affect patients experience of continuity of care.
Full description
Transition of care from hospital to home following orthopaedic surgery pose a significant risk to patient safety. After discharge, patients or primary care providers may need to communicate with the specialized healthcare team at the hospital about symptoms, postoperative complications, rehabilitation, wounds and medication, but are hampered by a fragmented healthcare system with slow communication pathways. Communication through phone often involves several intermediaries and waiting time for both patients and healthcare professionals. The fact that patients and healthcare professionals must be present at the same time is inflexible and disruptive to work processes. However, cross-sectoral communication and collaboration with patients after hospital discharge are prerequisites to achieve high-quality care and good patient outcomes. Review of the literature show that few studies have explored the effects of digital team-based communication with the patient and across sectors to facilitate collaboration and knowledge sharing after discharge. On the basis of findings from a preliminary pilot study suggesting asynchronous digital team-based communication between orthopaedic surgery patients and healthcare professionals across sectors (eDialogue) may be a solution to the existing problems in communication pathways, we initiated this trial.
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Inclusion and exclusion criteria
Patients are recruited from the following orthopaedic surgery sub-specialties at Aalborg University Hospital:
Inclusion Criteria:
Patients admitted and operated at Aalborg University Hospital, who;
Patients at all ages, but:
Have access to and ability to use a smartphone Have access to NemID (needed to create a GDPR-safe user profile in LetDialog)
Exclusion Criteria:
Patients, who:
Primary purpose
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Interventional model
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70 participants in 2 patient groups
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Central trial contact
Lili WH Jensen, MSc; Ole Rahbek, PhD, MD
Data sourced from clinicaltrials.gov
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