Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07024628

Assessing the Effectiveness of Heat Adaptation Digital Messages From Primary Care Providers to Their Patients on the Change in Behaviour for Heatwave-related Preparedness

Led by Hopital Montfort · Updated on 2025-06-17

20000

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

Sponsors

H

Hopital Montfort

Lead Sponsor

C

Children's Hospital of Eastern Ontario Research Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

Extreme heat events pose a significant health threat in Canada, as demonstrated by the 2021 heat wave that claimed over 600 lives in Western Canada. Most heat-related deaths occur indoors and are preventable. Primary care providers (PCPs), who serve 88% of Canadians, are uniquely positioned to identify and support at-risk individuals. Heat Smart, in alignment with Heat Alert and Response Systems (HARS), aims to bridge the gap between primary care and public health to enhance community resilience and reduce health inequities related to extreme heat events. This randomized control trial in Eastern Ontario will examine whether patients receiving tailored digital health messages from their family physician or nurse practitioner change their behaviour to protect themselves from extreme heat-related illness. The Heat Smart study will: * Assess risk: Analyze electronic medical records and patient surveys to identify vulnerable individuals. * Deliver tailored messages: Send personalized digital guidance via e-mail or text, offering heat safety advice and local resource information in English and French. * Issue early warning alerts: Notify at-risk patients of upcoming heat events, prompting action. * Evaluate impact: Use surveys and health data to measure effectiveness in reducing heat-related health impacts. Short-term outcomes include increased awareness and preparedness among patients about heat-related health risks. Long-term goals involve scaling the intervention across Canada to reduce heat-related illnesses, enhance social connectedness, and decrease healthcare utilization.

CONDITIONS

Official Title

Assessing the Effectiveness of Heat Adaptation Digital Messages From Primary Care Providers to Their Patients on the Change in Behaviour for Heatwave-related Preparedness

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Registered patients with a participating primary care provider
  • At least one visit with their primary care provider in the past two years
  • Have an active email, cell phone, or SMS service to receive digital messages
  • Able to understand and consent to participate in the study
  • Able to communicate in English or French
  • Patients recruited from primary care providers located in Eastern Ontario public health districts (including urban, rural, and Indigenous communities)
  • Primary care providers must be licensed family physicians or nurse practitioners in practices with at least 2 providers
  • Providers must offer comprehensive primary care (not only urgent or walk-in care)
  • Providers must use electronic medical records and expect to remain in practice for at least 24 months
  • Providers must be located in Eastern Ontario and willing to use the Canadian Primary Care Information Network and communication tools for outreach
Not Eligible

You will not qualify if you...

  • Patients who cannot read or understand English or French
  • Patients without an email address or text messaging service
  • Minors (under 18 years old)
  • Patients with dementia
  • Patients unable to read or write in English or French

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Institut du Savoir Montfort

Ottawa, Ontario, Canada, K1K0M9

Actively Recruiting

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Research Team

R

Rebecca A Tobin

CONTACT

W

William Hogg, Dr

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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