Reliability In Neurocognitive Telemedicine Screening (RING)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age65+
SponsorUniversity of British Columbia

About this trial

Perioperative neurocognitive disorders are common after surgery and pre-existing cognitive impairment is an important risk factor. Current guidelines recommend identifying cognitive impairment before surgery; however, screening remains inconsistent, particularly when preoperative assessments are performed remotely.

This prospective observational diagnostic validation study aims to determine whether a modified Mini-Cog cognitive screening tool administered by telephone can reliably identify cognitive impairment in patients aged 65 years and older undergoing preoperative assessment. Telephone-based modified Mini-Cog results will be compared with standard in-person Mini-Cog assessments to evaluate agreement and feasibility. This study may improve access to preoperative cognitive screening and support optimization of surgical care for older adults.

Eligibility criteria

Qualifiers

Patients with age >65 at time of listing for pre-operative assessment.

Patients with a conversational understanding of English language.

Patients scheduled for in-person consult with an anaesthesiologist.

Patients awaiting surgery at Vancouver General Hospital or University of British Columbia Hospital.

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Modified Mini-Cog Telephone Assessment

Treatment groups

No treatment groups listed

Sponsors and collaborators

University of British Columbia

Lead sponsor

Vancouver General Hospital

Collaborator