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Evaluating Patient Knowledge About Perioperative Neurocognitive Disorders (KNOW-PND Study)

Evaluating Patient Knowledge About Perioperative Neurocognitive Disorders (KNOW-PND Study)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05590845
Enrollment
100
Registered
2022-10-21
Start date
2023-01-15
Completion date
2024-12-15
Last updated
2024-12-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia Complication

Brief summary

Neurocognitive disorders remain one of the major perioperative complications. They are associated with delayed recovery, prolonged length of hospital stay and impacts on patients' quality of life. The incidence of PND ranges from 15-50%. While several causes have been investigated, PND seems to be due to the non-resolution of an inflammatory cascade, making some patients more at risk than others. As such, major risk factors include old age and lower education levels. As the global proportion of people aged 60 and above between 2015 and 2050 will increase from 12% to 22% and worldwide surgeries increases to \>300 million procedures per annum the incidence of perioperative neurocognitive disorders with high morbidity and mortality will go up. In 2015, the American Society of Anesthesiologists (ASA) launched the 'Perioperative Brain Health Initiative' to increase awareness about perioperative neurocognitive disorders. (PND) While physicians seems to be more and more aware about this condition, data regarding patient awareness are not available. An observational, single-centre, cross-sectional survey study (with initially a feasibility study) will be conducted in patients, 65 years and above undergoing elective total hip replacement surgery at AZ Sint-Jan (Brugge, Belgium) to assess patients' basic knowledge regarding PND.

Interventions

OTHERSurvey

Patients, 65 and above, scheduled for elective total hip replacement surgery, will be invited to participate in a survey (consisting of 15 questions) testing their knowledge regarding PND. After completion of the survey, patients will receive a standard preoperative brochure on anaesthesia-related topics and delirium. T-MOCA scores will be collected (22 = perfect score; \<18 = cutoff for cognitive impairment) (through a pre-operative telephone call). Six weeks post-operatively patients will once again be called for T-moca scores. Initially a feasibility study for 1/3 of sample size will be done.

Sponsors

Université Libre de Bruxelles
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
PND knowledge1 week pre-operativelyPatient knowledge regarding PND will be evaluated through 15 yes/no questions

Secondary

MeasureTime frameDescription
Baseline cognition1 week pre-operativelyBaseline T-moca scores will be documented in order to evaluate PND presence.
PND6 weeks post-operativelyT-moca scores will be documented post-operatively (and compared to baseline scores) in order to evaluate PND presence.

Countries

Belgium

Contacts

Primary ContactSarah Saxena, MD; PHD
sarah.saxena@ulb.ac.be+3250452111

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026