Web-based education program for cognitive health in surgical patients
A Web-Based Education Program in Promoting Brain Health During the Surgical Journey in Older Patients
This study tests a web-based education program to help older surgical patients understand brain health and the risks of cognitive issues after surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 150 (estimated) |
| Ages | 60 Years and up |
| Sex | All |
| Sponsor | University Health Network, Toronto Academic / other |
| Locations | 2 sites (Toronto, Ontario and 1 other locations) |
| Trial ID | NCT06540638 on ClinicalTrials.gov |
What this trial studies
This program aims to enhance brain health awareness among older surgical patients by providing a web-based educational platform. It focuses on informing patients about the risks of cognitive impairment and postoperative delirium, enabling them to make informed decisions regarding their health. Participants will engage in a 20-minute educational session that includes pre- and post-education questionnaires to assess knowledge gains and satisfaction with the program. The study will be conducted at two major hospitals in Toronto, targeting patients aged 60 and older who are scheduled for elective non-cardiac surgery.
Who should consider this trial
Good fit: Ideal candidates for this program are patients aged 60 and older who are undergoing elective non-cardiac surgery and have basic computer skills.
Not a fit: Patients with previous major neurocognitive disorders or uncontrolled psychiatric conditions may not benefit from this educational intervention.
Why it matters
Potential benefit: If successful, this program could empower older patients to better manage their cognitive health and reduce the risk of postoperative complications.
How similar studies have performed: Other studies have shown that educational interventions can significantly improve patient outcomes and awareness, suggesting a positive outlook for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * patients ≥60 years old * undergoing elective non-cardiac surgery * competent to provide informed consent in English and * possess some computer skills Exclusion Criteria: * previous major neurocognitive disorder * uncontrolled psychiatric disorders * hearing and/or vision impairment
Where this trial is running
Toronto, Ontario and 1 other locations
- 399 Bathurst St. Toronto Western Hospital, Preadmission Clinic, Dept. of Anesthesia — Toronto, Ontario, Canada (Recruiting)
- Mount Sinai Hospital — Toronto, Ontario, Canada (Recruiting)
Study contacts
- Principal investigator: Frances Chung, MBBS, FRCPC — University Health Network, Toronto
- Study coordinator: Sazzadul Islam, M.Sc.
- Email: sazzadul.islam@uhn.ca
- Phone: 4166035800
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.