NCT04105036

Brief Summary

Social deprivation is a state to which older adults may be exposed, leading to adverse social, psychological, and health outcomes. Social deprivation may be more sensitive than socioeconomic status for predicting adversity while using only a few items for evaluation. However, there is no practical assessment for social deprivation in older Canadian adults. Two indices that capture a broad picture of social vulnerability have previously been developed for older Canadians. Using participants in the Canadian Longitudinal Study on Aging (CLSA), the overall objective is to examine and compare the associations of the COAD score and index, as well as the Keefe et al. and Andrew et al. indices with prevalent and incident adverse social, psychological, and health outcomes in participants at baseline assessment.

Trial Health

55
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
30,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Apr 2020

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

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

September 23, 2019

Completed
3 days until next milestone

First Posted

Study publicly available on registry

September 26, 2019

Completed
6 months until next milestone

Study Start

First participant enrolled

April 1, 2020

Completed
4.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2025

Completed
Last Updated

September 19, 2024

Status Verified

September 1, 2024

Enrollment Period

4.9 years

First QC Date

September 23, 2019

Last Update Submit

September 16, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Social Deprivation

    EPICES ( Évaluation de la Précarité et des Inégalités de santé dans les Centres d'Examens de Santé) scale, the cutoff 30.17 will be used

    1 day

Secondary Outcomes (14)

  • Polypharmacy

    1 day

  • Comorbidities

    1 day

  • Mortality

    1 day

  • Depression

    1 day

  • Falls

    1 day

  • +9 more secondary outcomes

Study Arms (4)

45-54 years of age

Divided into two subgroups: individuals who are and are not socially deprived

Other: Data Collection

54-64 years of age

Divided into two subgroups: individuals who are and are not socially deprived

Other: Data Collection

65-74 years of age

Divided into two subgroups: individuals who are and are not socially deprived

Other: Data Collection

75-85 years of age

Divided into two subgroups: individuals who are and are not socially deprived

Other: Data Collection

Interventions

Telephone interview questionnaire, in-home face-to-face interview, and data from the Collection Site

45-54 years of age54-64 years of age65-74 years of age75-85 years of age

Eligibility Criteria

Age45 Years - 85 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Individuals eligible for this study will be the participants of the CLSA

You may qualify if:

  • Participants of the comprehensive CLSA assessment.

You may not qualify if:

  • No information on social status
  • No information on social, psychological, and health outcomes

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Jewish General Hospital

Montreal, Quebec, H3T 1E2, Canada

Location

MeSH Terms

Interventions

Data Collection

Intervention Hierarchy (Ancestors)

Epidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Olivier Beauchet, MD

    McGill University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 23, 2019

First Posted

September 26, 2019

Study Start

April 1, 2020

Primary Completion

March 1, 2025

Study Completion

March 1, 2025

Last Updated

September 19, 2024

Record last verified: 2024-09

Locations