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Resource Navigators for Caregiver Burnout

N/A
Recruiting
Research Sponsored by Unity Health Toronto
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, and 6 months.
Awards & highlights
No Placebo-Only Group

Summary

This trial tests how a resource navigator can help care home staff access health and wellness resources, to improve their wellness, burnout, and vaccine uptake.

Who is the study for?
This trial is for full-time or part-time employees aged 18 and older who work in Ontario long-term care or retirement homes, including PSWs and support staff. Participants must be comfortable with English and willing to use email for study communications.
What is being tested?
The trial tests if resource navigators can improve the wellness of long-term care and retirement home staff by providing one-on-one support. It compares a group with navigator access to a control group without it, focusing on wellness, burnout, vaccine status, and COVID-19 outcomes.
What are the potential side effects?
Since this intervention involves non-medical assistance rather than drugs or medical procedures, traditional side effects are not expected. However, there may be indirect effects on stress levels or emotional well-being.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, and 6 months.
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, and 6 months. for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Rate of Change in Wellness
Secondary study objectives
Rate Changes in number of participants with COVID-19 vaccination, number of participants with COVID infection and hospitalization, over time
Rate of Change in Level of Burnout
Rate of Changes in knowledge, access to and use of wellness supports

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Intervention GroupExperimental Treatment1 Intervention
Receiving sessions with a resource navigator 2x a month, and monthly resources.
Group II: ControlActive Control1 Intervention
Receiving monthly resources only
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Intervention
2011
Completed Phase 4
~73780

Find a Location

Who is running the clinical trial?

Unity Health TorontoLead Sponsor
562 Previous Clinical Trials
453,777 Total Patients Enrolled
Canadian Institutes of Health Research (CIHR)OTHER_GOV
1,394 Previous Clinical Trials
26,527,684 Total Patients Enrolled
University of TorontoOTHER
725 Previous Clinical Trials
1,115,522 Total Patients Enrolled
~7 spots leftby Mar 2025
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