An interventional study of Heat adaptation digital messaging and Non-heat-related digital messaging in Heathly Subjects, Primary Health Care and Climate Change, sponsored by Hopital Montfort. Recruiting at 1 site in Canada. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-18.
Sponsored by Hopital Montfort · Not applicable, Interventional, and Prevention
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:
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.
Primary Hypothesis
The study will test the following primary hypothesis: "Patients who receive tailored digital health promotion messages from their primary care providers will perform more heat adaptive proactive behaviours to protect themselves from heat-related illness compared to those who do not receive such messages."
Secondary Hypotheses
This study employs a cluster randomized controlled trial (RCT) to evaluate the impact of a heat adaptation digital messages intervention. Only primary care practices with at least 2 participating practitioners will be included in the study, where each PCP will act as a patient cluster. For each practice, the Primary Care Providers will be randomly assigned, and all their adult patient panel will either receive heat smart adaptation digital messages (the exposed group) or non-heat wave health promotion digital messages (the control group).
The study follows an intention-to-treat (ITT) design, meaning that all participants who consent to participate will be analyzed based on their original group assignment, regardless of adherence to the heat smart digital messages intervention (e.g., did the participant read the message). The study will have a two-year follow-up period to assess behavioural changes related to heat adaptation.
Research Objectives
The Heat Smart project aims to enhance primary care involvement in public health led heat adaptation strategies and improve the preparedness of at-risk populations for extreme heat events.
Assess Individual-Level Risks for Excessive Heat-Related Illnesses
Characterize socio-cultural, demographic, and clinical factors that contribute to heat vulnerability, including:
Implement and Evaluate a Digital Messaging Intervention
Deliver tailored, evidence-based digital messages (via email or text) to all adult patients of participating primary care providers to:
Evaluate the impact of the intervention through:
Scale and Expand the Intervention
Improve Health Equity and Climate Resilience
These objectives align with Canada's HeatADAPT Program and National Adaptation Strategy, ensuring a whole-of-society approach to protecting health during extreme heat events.
Randomization
291 studies on the registry are indexed under Risk Reduction Behavior; 39 are open to participants now.
This study's planned enrollment of 20,000 is above the median of 201 across 250 interventional studies indexed under Risk Reduction Behavior.
Browse Risk Reduction Behavior studies →Hopital Montfort is the lead sponsor of 13 studies on the registry; 3 are open to participants now.
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Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
The Heat Smart randomized controlled trial study will recruit patients and primary care providers (PCPs) from Eastern Ontario. The inclusion criteria ensure that the intervention reaches at-risk individuals while being scalable across different patient populations:
Primary Care Patients:
Primary Care Providers:
Exclusion Criteria:
Patients who do not read French or English will be excluded from the study as they will not be able to give or to fill out the surveys. Patients who do not have an email address or text messaging service will be excluded for the same reason. Minors, patients with dementia and people who cannot read and write in English or French will not be eligible because the automated approach to surveying patients makes it impractical to properly obtain their consent.
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Patients in the Treated arm will receive messages to equip and prepare them for extreme heat events. The intervention is multifaceted: the first message will to encourage patients to prepare by creating a heat safety plan, and to form Check-in Companion groups among friends, neighbours, and relatives as well as to connect patients with existing key infrastructure that can be vital during heat events (ex: cooling stations and public facilities with air conditioning). When a heat-advisory is announced, additional messages will be sent to alert patients in the Treated group to activate their heat safety plans.
Other: Heat adaptation digital messaging
Patients in the Control arm will receive messages not related to heat waves. These messages will be related to other environmental risks
Other: Non-heat-related digital messaging
Digital messages to equip and prepare patients for extreme heat events. The first message will to encourage patients to prepare by creating a heat safety plan, and to form Check-in Companion groups among friends, neighbours, and relatives as well as to connect patients with existing key infrastructure that can be vital during heat events (ex: cooling stations and public facilities with air conditioning). When a heat-advisory is announced, additional messages will be sent to alert patients in the Treated group to activate their heat safety plans.
Digital health promotion messages not related to heatwaves
Number of participants who report adopting at least one heat adaptation behaviour via self-report survey
Participants will be asked: "Have you taken any action to prepare for a heat wave?" (yes/no).
Time frame: Assessed after a heatwave event, up to 2 years following enrollment.
Number of heat-adaptation behaviours self-reported by the participants.
Participants will be asked a question about which heat-adaptive behaviours they undertook prior to the most recent heat wave.
Time frame: Assessed after a heatwave event, up to 2 years following enrollment.
Self-reported heatwave-related challenges: frequency of economic and lifestyle impacts
Participants will select from a list of impacts (e.g., missed work, medical costs, utility bills, missed activities, increased caregiving responsibilities). Results will be reported as the proportion selecting each option.
Time frame: Assessed after a heatwave event, up to 2 years following enrollment.
Heatwave health risk and preparedness beliefs - Likert scores
Participants will respond to three belief statements on a 5-point Likert scale (1 = Strongly Disagree, 5 = Strongly Agree): 1. If I do not take steps to cool my home, keep my body cool, or stay hydrated during a heatwave, I may experience a medical emergency 2. I believe I have the resources and information needed to avoid a medical emergency during a heatwave. 3. Staying in touch with someone during a heatwave is important for my health.
Time frame: Assessed after a heatwave event, up to 2 years following enrollment.
Frequency of social interactions during heatwaves
Participants will report number of in-person or virtual interactions during the most recent heatwave using categorical options (none; 1-3; 4-6; 7+). Responses will be summarized as proportions by category.
Time frame: Assessed after a heatwave event, up to 2 years following enrollment.
Knowledge of heat waves - score based on number of correct answers
Four true/false questions assessing understanding of the health risks of heatwaves
Time frame: Assessed after a heatwave event, up to 2 years following enrollment.
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