Determining Postoperative Recovery and the Impact of Adverse Events in Neurosurgery Based on Self-reported, App-based Longitudinal Assessment
Recruiting
Observational Study
Disc Disease
Instabilities Lumbar
Brain Tumor
Aneurysm
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 400 (estimated)
- Sponsor
- Cantonal Hospital of St. Gallen · Other
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About This Trial
Analyzing the impact of surgery and adverse events (AEs) on patients' well-being is of paramount importance as it provides essential information for benefit-risk assessment. Current methods in outcome research are static, resource-intensive and subject to missing-data issues. Moreover, AEs are inconsistently reported using various grading systems that usually do not account for patients' subjectiv…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age ≥ 18 years
* The patient must be able to consent
* The patient is willing to provide data upon one year after surgery
* The patient possesses and is capable of using a smartphone (Android or iOS operative systems)
* The patient has the necessary language and cognitive skil…
Contacts