NCT05653154

Brief Summary

This study will examine preoperative concerns in older adults through the use of a self-administered questionnaire. The development of this questionnaire will involve adapting survey questions from previously validated studies, creating new questions, and generating a comprehensive questionnaire.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
264

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Dec 2022

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 29, 2022

Completed
16 days until next milestone

Study Start

First participant enrolled

December 15, 2022

Completed
1 day until next milestone

First Posted

Study publicly available on registry

December 16, 2022

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 23, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 23, 2024

Completed
Last Updated

April 13, 2025

Status Verified

April 1, 2025

Enrollment Period

1.9 years

First QC Date

November 29, 2022

Last Update Submit

April 9, 2025

Conditions

Cognitive Impairment

Keywords

Elderly, surgical

Outcome Measures

Primary Outcomes (1)

  • preoperative concerns

    current daily functional status

    1 day

Secondary Outcomes (1)

  • Cognitive assessments

    1 day

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Surgical patients

You may qualify if:

  • Older adults, who are aged 65 or older and
  • Medical patients in geriatric clinic or surgical inpatients in pre-operative clinics

You may not qualify if:

  • Lack English language capability

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

399 Bathurst St., Toronto Western Hospital, Dept. of Anesthesia

Toronto, Ontario, M5T2S8, Canada

Location

Mount Sinai Hospital

Toronto, Ontario, Canada

Location

MeSH Terms

Conditions

Cognitive Dysfunction

Condition Hierarchy (Ancestors)

Cognition DisordersNeurocognitive DisordersMental Disorders

Study Officials

  • Frances Chung, MBBS MD FRCPC

    University Health Network, Toronto

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Anesthesiologist

Study Record Dates

First Submitted

November 29, 2022

First Posted

December 16, 2022

Study Start

December 15, 2022

Primary Completion

October 23, 2024

Study Completion

October 23, 2024

Last Updated

April 13, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will not share

Locations

CA(2)