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

This trial does not accept healthy volunteers

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 population

This study will include adults aged 65 years and older who are scheduled for elective surgery and undergoing preoperative anesthetic assessment at Vancouver General Hospital or University of British Columbia Hospital. Participants will be recruited from the Pre-Admission Clinic referral list and will complete a modified Mini-Cog cognitive screening assessment by telephone followed by a standard in-person Mini-Cog assessment during their preoperative visit. The study population represents older adults undergoing surgical evaluation who do not have a known diagnosis of cognitive impairment.

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • Modified Mini-Cog Telephone Assessment

    Diagnostic test

    A modified Mini-Cog cognitive screening assessment administered by telephone to evaluate its reliability and concordance with standard in-person Mini-Cog assessment in older adults undergoing preoperative assessment.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Concordance between telephone-administered modified Mini-Cog and standard in-person Mini-Cog assessment

Agreement between modified Mini-Cog scores obtained by telephone and standard in-person Mini-Cog scores in identifying cognitive impairment using the established Mini-Cog cutoff score.

Time frame
Within 1-2 weeks of telephone assessment

Secondary outcomes

1

Sensitivity and specificity of telephone modified Mini-Cog

Sensitivity and specificity of the telephone-administered modified Mini-Cog for detection of cognitive impairment compared with the in-person Mini-Cog assessment.

Time frame
Within 1-2 weeks of telephone assessment
2

Completion time of modified Mini-Cog assessment

Time required to complete the telephone and in-person Mini-Cog assessments.

Time frame
During each assessment
3

Feasibility of telephone-based cognitive screening

Proportion of participants able to complete the telephone-administered modified Mini-Cog assessment.

Time frame
During telephone assessment

Other outcomes

Sponsors and contacts

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University of British Columbia

Lead sponsor

Vancouver General Hospital

Collaborator