Heathly SubjectsHeatSmartNCT07024628
Assessing the Effectiveness of Heat Adaptation Digital Messages From Primary Care Providers to Their Patients on the Change in Behaviour for Heatwave-related Preparedness
A study testing Heat adaptation digital messaging and Non-heat-related digital messaging in people with Heathly Subjects and Primary Health Care, run by Hopital Montfort at 1 site in Canada.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Heathly Subjects, Primary Health Care, Climate Change
- What is being tested?
- Heat adaptation digital messaging and Non-heat-related digital messaging
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 20,000 participants
- Where
- 1 siteCanada
- Study dates
- 1 Apr 2025to 31 Mar 2028
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- 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:
- Adults (18 years and older)
- Patients must be registered with a participating PCP.
- They must have had at least one visit with their PCP in the past two years to ensure active engagement.
- Participants must have an active email, cell phone or messaging service (SMS) to receive Heat Smart digital messages.
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- Patients must be able to understand and consent to participate in the study.
- Patients must be able to communicate in at least one of the official languages (English, French).
- Participants will be recruited from PCP located in two Eastern Ontario public health districts: the Eastern Ontario Health Unit and Ottawa Public Health (including urban, rural, and Indigenous communities such as Akwesasne).
- Primary Care Providers:
- Must be a licensed Family Physician (FP) or Nurse Practitioner (NP) in a practice of at least 2 PCPS.
- The providers must be offering comprehensive primary care to a panel of patients (not solely urgent care or walk-in services).
- Must work in a computerized primary care clinic with an electronic medical record system.
- Must expect to remain in practice for at least 24 months.
- Must be located in Eastern Ontario.
- Must be willing to use the Canadian Primary Care Information Network (CPIN) to deliver Heat Smart messages and surveys.
- Must be using Cliniconex or Qualtrics as a practice tool for communication enabling outreach before the patients are invited to consent to participate in the study.
Who cannot join
- 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.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
William Hogg, Dr contact
Canada1 site, 1 recruiting
- Recruiting
Institut du Savoir Montfort
Ottawa, Ontario, K1K0M9
Rebecca A Tobin, 613-746-4621 ext. 6014, rebeccatobin@montfort.on.ca
William Hogg, Dr, whogg@uottawa.ca
About this study
Official title: Heat Smart: Empowering Primary Care Providers to Safeguard Vulnerable Populations Against Extreme Heat
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:
Read more
- 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.
Read the detailed description
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
- Patients receiving Heat Smart messages will demonstrate greater engagement in specific heat preparedness activities, such as creating heat safety plans and forming networks among friends, neighbours, and relatives (patient survey data).
- Patients in the intervention group will experience lower rates of heat-related healthcare utilization, as measured by primary care provider visits, emergency department visits and filling prescription drugs during heat events (ICES data).
- The intervention will be effective across different socio-demographic subpopulations, including older adults, individuals with chronic illnesses, and socially isolated individuals.
- The integration of primary care into HARS will enhance public health system coordination and improve response strategies for extreme heat events.
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:
- Age (older adults, children)
- Chronic illnesses (e.g., cardiovascular disease, diabetes, asthma, mental health conditions)
- Social isolation and poverty
- Use of medications that impair thermoregulation
- 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:
- Educate them on heat-related health risks.
- Encourage the development of personalized heat safety plans for patients at increased risk.
- Provide information about local cooling stations, transportation options, and emergency resources.
- Issue early warning alerts to at-risk patients when excessive heat events are imminent.
- Evaluate the impact of the intervention through:
- Patient surveys assessing self-reported behaviour change in heat preparedness.
- Linking patient survey responses to health administrative data to measure healthcare utilization (e.g., emergency department visits, prescription medication use).
- Determine the effectiveness of integrating primary care providers into public health-led Heat Alert and Response Systems (HARS).
- Scale and Expand the Intervention
- Refine and adapt the intervention based on rapid-cycle evaluations.
- Expand to two additional provinces to test scaling feasibility.
- Develop a national model for integrating primary care into climate adaptation strategies, ensuring scalability and sustainability.
- Improve Health Equity and Climate Resilience
- Target vulnerable and equity-deserving populations, ensuring that interventions are tailored to their needs.
- Encourage social connectedness by fostering Check-in Companion heat response groups among friends, neighbours, and relatives.
- Enhance collaboration between primary care and public health to create a cohesive, system-wide approach to adaptation to extreme heat events.
- Provide policy-relevant insights to inform national heat adaptation strategies and reduce health inequities.
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
- Patients will be assigned to intervention or control arms using cluster randomization. Block of sizes of 2 will be used to randomly assign the primary care provider to either the treatment or control arms, to ensure balance between groups and between practices.
- After randomization, balance across the two arms will be assessed using variables associated with vulnerability (e.g., age, sex, housing marginalization (ONT-Marg, based on 6-digit postal code) is included as a covariate to account for socio-economic disparities in vulnerability to heat-related events, neighbourhood rurality, self-reported baseline Heat Action Plan, chronic illness (e.g., cardiovascular disease, diabetes, asthma, mental health conditions) and heat susceptible diseases (e.g., requiring medications that impair thermoregulation)).
- Conditions
- Heathly Subjects, Primary Health Care, Climate Change, Public Health, Preventive Health Services (PREV HEALTH SERV), Environmental Exposure
- Being tested
- Heat adaptation digital messaging, Non-heat-related digital messaging
- Keywords
- primary care, digital messaging, heatwave, climate change, public health, CPIN
- Medical subject headings
- Risk Reduction Behavior, Heat Stress Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Heat adaptation digital messagingOther
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.
Non-heat-related digital messagingOther
Digital health promotion messages not related to heatwaves
| Study group | Role | What they receive |
|---|---|---|
| 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. Receives: Other: Heat adaptation digital messaging |
| 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 Receives: Other: Non-heat-related digital messaging |
What is being measured
The primary outcome is the main question the study is designed to answer.
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).
Measured: Assessed after a heatwave event, up to 2 years following enrollment.
Secondary outcomes (1)
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.
Measured: Assessed after a heatwave event, up to 2 years following enrollment.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Jun 2025
- Study start1 Apr 2025
- Primary completionSep 2027 (estimated)
- Study completion31 Mar 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Heathly SubjectsStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- 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.
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 20,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Hopital Montfort
- Sponsor type
- University, hospital or other
- Collaborators
- Children's Hospital of Eastern Ontario Research Institute
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07024628
- Sponsor's protocol ID
- 24-25-02-055
- Acronym
- HeatSmart
- Status last verified
- Aug 2026
- First submitted
- 28 May 2025
- Last updated
- 18 Sep 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 18 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Heat Smart: Empowering Primary Care Providers to Safeguard Vulnerable Populations Against Extreme Heat
- ClinicalTrials.gov ID
- NCT07024628
- Acronym / sponsor ID
- HeatSmart / 24-25-02-055
- Conditions
- Heathly Subjects, Primary Health Care, Climate Change, Public Health, Preventive Health Services (PREV HEALTH SERV), Environmental Exposure
- Keywords
- primary care, digital messaging, heatwave, climate change, public health, CPIN
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 20,000 participants (estimated)
- Lead sponsor
- Hopital MontfortUniversity, hospital or other
- Collaborators
- Children's Hospital of Eastern Ontario Research Institute
- Study start
- 1 Apr 2025 (actual)
- Primary completion
- Sep 2027 (estimated)
- Study completion
- 31 Mar 2028 (estimated)
- First posted
- 17 Jun 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
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
- Patients receiving Heat Smart messages will demonstrate greater engagement in specific heat preparedness activities, such as creating heat safety plans and forming networks among friends, neighbours, and relatives (patient survey data).
- Patients in the intervention group will experience lower rates of heat-related healthcare utilization, as measured by primary care provider visits, emergency department visits and filling prescription drugs during heat events (ICES data).
- The intervention will be effective across different socio-demographic subpopulations, including older adults, individuals with chronic illnesses, and socially isolated individuals.
- The integration of primary care into HARS will enhance public health system coordination and improve response strategies for extreme heat events.
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:
- Age (older adults, children)
- Chronic illnesses (e.g., cardiovascular disease, diabetes, asthma, mental health conditions)
- Social isolation and poverty
- Use of medications that impair thermoregulation
- 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:
- Educate them on heat-related health risks.
- Encourage the development of personalized heat safety plans for patients at increased risk.
- Provide information about local cooling stations, transportation options, and emergency resources.
- Issue early warning alerts to at-risk patients when excessive heat events are imminent.
- Evaluate the impact of the intervention through:
- Patient surveys assessing self-reported behaviour change in heat preparedness.
- Linking patient survey responses to health administrative data to measure healthcare utilization (e.g., emergency department visits, prescription medication use).
- Determine the effectiveness of integrating primary care providers into public health-led Heat Alert and Response Systems (HARS).
- Scale and Expand the Intervention
- Refine and adapt the intervention based on rapid-cycle evaluations.
- Expand to two additional provinces to test scaling feasibility.
- Develop a national model for integrating primary care into climate adaptation strategies, ensuring scalability and sustainability.
- Improve Health Equity and Climate Resilience
- Target vulnerable and equity-deserving populations, ensuring that interventions are tailored to their needs.
- Encourage social connectedness by fostering Check-in Companion heat response groups among friends, neighbours, and relatives.
- Enhance collaboration between primary care and public health to create a cohesive, system-wide approach to adaptation to extreme heat events.
- Provide policy-relevant insights to inform national heat adaptation strategies and reduce health inequities.
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
- Patients will be assigned to intervention or control arms using cluster randomization. Block of sizes of 2 will be used to randomly assign the primary care provider to either the treatment or control arms, to ensure balance between groups and between practices.
- After randomization, balance across the two arms will be assessed using variables associated with vulnerability (e.g., age, sex, housing marginalization (ONT-Marg, based on 6-digit postal code) is included as a covariate to account for socio-economic disparities in vulnerability to heat-related events, neighbourhood rurality, self-reported baseline Heat Action Plan, chronic illness (e.g., cardiovascular disease, diabetes, asthma, mental health conditions) and heat susceptible diseases (e.g., requiring medications that impair thermoregulation)).
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
- Model description
- 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.
| Arm | Type | Receives |
|---|---|---|
| Treated - receive heat adaptation digital messages | Experimental | Other: Heat adaptation digital messagingPatients 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. |
| Control | Active comparator | Other: Non-heat-related digital messagingPatients in the Control arm will receive messages not related to heat waves. These messages will be related to other environmental risks |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (17 listed)
- 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:
- Adults (18 years and older)
- Patients must be registered with a participating PCP.
- They must have had at least one visit with their PCP in the past two years to ensure active engagement.
- Participants must have an active email, cell phone or messaging service (SMS) to receive Heat Smart digital messages.
Key exclusion criteria (1 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Heat adaptation digital messagingDigital 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. | Other | Treated - receive heat adaptation digital messages |
| Non-heat-related digital messagingDigital health promotion messages not related to heatwaves | Other | Control |
Primary outcome
Number of participants who report adopting at least one heat adaptation behaviour via self-report survey
Time frame: Assessed after a heatwave event, up to 2 years following enrollment.
Participants will be asked: "Have you taken any action to prepare for a heat wave?" (yes/no).
1 secondary outcome
Number of heat-adaptation behaviours self-reported by the participants.
Time frame: Assessed after a heatwave event, up to 2 years following enrollment.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Sep 2026.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
William Hogg, Dr contact
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Heat adaptation digital messaging and Non-heat-related digital messaging in people with Heathly Subjects and Primary Health Care, run by Hopital Montfort at 1 site in Canada.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 17 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 18 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Rebecca A Tobin (613-746-4621 ext. 6014, rebeccatobin@montfort.on.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of participants who report adopting at least one heat adaptation behaviour via self-report survey (time frame: Assessed after a heatwave event, up to 2 years following enrollment.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Sep 2026.