Supporting the Wellness of Ontario Physicians During COVID-19

NCT ID: NCT04803812

Last Updated: 2021-11-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

19124 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-01-26

Study Completion Date

2021-09-02

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

In light of the coronavirus pandemic, the challenge of physician burnout has taken on a new urgency. Long-hours and difficult, sometimes unsafe work conditions are creating a severe strain for emergency physicians and others on the frontlines of Ontario's response to COVID-19. There are a variety of evidence-informed ways that physicians can protect their wellbeing with modest investments of time and energy that will be applied. The evaluation will be a randomized trial comparing the outcomes from each of the three treatment arms. Researchers may also use a pre-post comparison with control parameters to conduct an exploratory analysis to assess efficacy.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Mental Health Wellness 1 Anxiety Happiness

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

DOUBLE

Participants Caregivers

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Receive weekly SMS containing wellness stories shared by other Ontario physicians

Group Type EXPERIMENTAL

Remote SMS (short message service, also known as "text message") delivery

Intervention Type OTHER

Assessing the comparative effects of SMS types (storytelling; resources/strategies; and a combination of both) on physician wellbeing.

Receive weekly SMS containing aim wellness resources/strategies.

Group Type EXPERIMENTAL

Remote SMS (short message service, also known as "text message") delivery

Intervention Type OTHER

Assessing the comparative effects of SMS types (storytelling; resources/strategies; and a combination of both) on physician wellbeing.

Receive weekly SMS combining wellness stories & resources/strategies

Group Type EXPERIMENTAL

Remote SMS (short message service, also known as "text message") delivery

Intervention Type OTHER

Assessing the comparative effects of SMS types (storytelling; resources/strategies; and a combination of both) on physician wellbeing.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Remote SMS (short message service, also known as "text message") delivery

Assessing the comparative effects of SMS types (storytelling; resources/strategies; and a combination of both) on physician wellbeing.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Active membership to the Ontario Medical Association (OMA). Up-to-date cell phone information registered to the OMA.

Exclusion Criteria

* Participation in the OMA Physician Burnout Task Force. Opt-out from the intervention.
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

The Behavioural Insights Team

OTHER

Sponsor Role collaborator

Ontario Medical Association

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

James Wright

Role: PRINCIPAL_INVESTIGATOR

Ontario Medical Association

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Ontario Medical Association

Toronto, Ontario, Canada

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Canada

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

39707

Identifier Type: -

Identifier Source: org_study_id