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| Name | Class |
|---|---|
| Children's Hospital of Eastern Ontario Research Institute | OTHER |
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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
Identify patients at increased risk of heat-related illness using primary care provider's electronic medical records and patient surveys.
Characterize socio-cultural, demographic, and clinical factors that contribute to heat vulnerability, including:
Segment patients into subpopulations based on shared characteristics to tailor interventions.
Assess patients' information needs and barriers to heat preparedness.
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:
Issue early warning alerts to at-risk patients when excessive heat events are imminent.
Evaluate the impact of the intervention through:
Determine the effectiveness of integrating primary care providers into public health-led Heat Alert and Response Systems (HARS).
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
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Treated - receive heat adaptation digital messages | Experimental | 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. |
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| Control | Active Comparator | Patients in the Control arm will receive messages not related to heat waves. These messages will be related to other environmental risks |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Heat adaptation digital messaging | Other | 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. |
| Measure | Description | Time Frame |
|---|---|---|
| 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). | Assessed after a heatwave event, up to 2 years following enrollment. |
| Measure | Description | Time Frame |
|---|---|---|
| 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. | Assessed after a heatwave event, up to 2 years following enrollment. |
| Measure | Description | Time Frame |
|---|---|---|
| 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. | Assessed after a heatwave event, up to 2 years following enrollment. |
Inclusion Criteria:
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 informed consent 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.
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Rebecca A Tobin | Contact | 613-746-4621 | 6014 | rebeccatobin@montfort.on.ca |
| William Hogg, Dr | Contact | whogg@uottawa.ca |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Institut du Savoir Montfort | Recruiting | Ottawa | Ontario | K1K0M9 | Canada |
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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).
There will be continuous recruitment through the study. Outcomes will be assessed after each heatwave. This means that participants enrolled at the start of the study will have a greater number of timepoints for data collection.
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| Non-heat-related digital messaging | Other | Digital health promotion messages not related to heatwaves |
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| 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):
| 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. | 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 | Assessed after a heatwave event, up to 2 years following enrollment. |
| ID | Term |
|---|---|
| D040242 | Risk Reduction Behavior |
| D018882 | Heat Stress Disorders |
| ID | Term |
|---|---|
| D001519 | Behavior |
| D014947 | Wounds and Injuries |
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