Understanding Patient Knowledge About Neurocognitive Disorders Related to Surgery
Evaluating Patient Knowledge About Perioperative Neurocognitive Disorders (KNOW-PND Study)
This study is trying to see how much older patients know about memory problems that can happen after hip surgery and anesthesia, to help improve their understanding and recovery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 65 Years and up |
| Sex | All |
| Sponsor | Université Libre de Bruxelles Academic / other |
| Locations | 1 site (Bruges) |
| Trial ID | NCT05590845 on ClinicalTrials.gov |
What this trial studies
This observational study aims to evaluate the level of knowledge patients have regarding perioperative neurocognitive disorders (PND), which are significant complications associated with anesthesia. The study focuses on patients aged 65 and older who are scheduled for elective hip surgery, assessing their awareness of the risks and implications of PND. By utilizing surveys, the research seeks to identify gaps in patient knowledge that could impact their recovery and quality of life. The findings may help inform educational initiatives to better prepare patients for surgery.
Who should consider this trial
Good fit: Ideal candidates for this study are patients aged 65 and older who are scheduled for elective hip surgery and have an ASA score of 1 to 3.
Not a fit: Patients who do not speak Dutch or have known neuropsychiatric conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance patient education and awareness, potentially leading to improved outcomes and quality of life for older surgical patients.
How similar studies have performed: While there is ongoing research into perioperative neurocognitive disorders, this specific focus on patient knowledge is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * age 65 and above * ASA score 1 to 3 * scheduled for elective hip surgery. Exclusion Criteria: * insufficient knowledge of Dutch * known neuropsychiatric conditions
Where this trial is running
Bruges
- AZ Sint-Jan Brugge Oostende AV — Bruges, Belgium (Recruiting)
Study contacts
- Principal investigator: Sarah Saxena, MD;PHD — AZ Sint-Lucas Brugge
- Study coordinator: Sarah Saxena, MD; PHD
- Email: sarah.saxena@ulb.ac.be
- Phone: +3250452111
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.