ACTRN12619001778178
Recruiting
未知
Perioperative Enhancement to improve the Cognitive Trajectory of older patients undergoing cardiac and non-cardiac surgery (The PROTECT trial)
ConditionsDeliriumPostoperative Neurocognitive DisorderMild Neurocognitive DisorderMajor Neurocognitive DisorderAnaesthesiology - AnaestheticsNeurological - Neurodegenerative diseasesPublic Health - Health promotion/educationSurgery - Other surgeryMental Health - Studies of normal psychology, cognitive function and behaviour
Overview
- Phase
- 未知
- Status
- Recruiting
- Sponsor
- The University of Melbourne
- Enrollment
- 692
Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- Randomised controlled trial
- Primary Purpose
- Prevention
- Masking
- Blinded (masking used)
Eligibility Criteria
- Ages
- 65 Years to o limit (—)
- Sex
- All
Inclusion Criteria
- •1\. Patients aged 65 years or older, scheduled for cardiac or non\-cardiac surgery, requiring at minimum, one night hospital stay
- •2\. Reside within a reasonable proximity to St Vincent's Hospital Melbourne to facilitate neuropsychology follow up and participation with intervention strategies.
- •3\. Capacity to provide written informed consent
Exclusion Criteria
- •1\. Prior neurological injury or insult (e.g., major traumatic brain injury)
- •2\. Contraindication to neuropsychological testing such as language, visual or hearing impairment
- •3\. Associated medical problems that may lead to significant complications and subsequent loss to follow or inability to engage with prehabilitation activities.
- •4\. Patients unable to consent independently to their surgery on account of cognitive impairment
Investigators
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