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Can wearable sensors unlock the hidden health toll of heat waves?

NCT ID NCT06850025

Knowledge-focused Sponsor: Institut National de la Santé Et de la Recherche Médicale, France Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jul 31, 2026 · Last updated Jul 31, 2026

Summary

This study uses wearable sensors to track how heat exposure during daily activities affects the body, sleep, and wellbeing in 180 adults aged 30-64 living in the Ile-de-France region. Participants wear bracelets that measure skin temperature, blood pressure, and movement, along with sensors to gauge personal heat stress. The goal is to understand which environmental and behavioral factors contribute to heat stress and how that stress impacts sleep and overall health. The findings could inform strategies to protect people during hot weather.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Wearable sensors and mobile sensing technology to measure heat stress, sleep, and wellbeing
What this could lead to
If successful, this could reveal how heat exposure in daily life affects health and sleep, potentially guiding urban design and public health advice to reduce heat-related harm.
What could go wrong
This is an observational study, so it cannot prove cause and effect. Results may be limited by the specific region and participant group, and personal factors could influence the measurements.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 180 people

The number the study aims to enrol. It can still change while the study runs.

Started

Feb 2025

Expected to finish

Feb 2035

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population is a sample recruited through internet advertisement, residing in the Grand Paris, in warmer or cooler areas and in different types of dwellings. Quota sampling is applied in this research.

Ages

30 to 64 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Person aged between 30-64 years * Person living in the Ile-de-France Exclusion Criteria: * Person subject to a legal protection measure (safeguarding of justice, curatorship, guardianship) * Person deprived of liberty by a judicial or administrative decision, * Person with a major functional limitation affecting their spatial mobility * Person unable to complete a questionnaire * Known cardiovascular (other than hypertension) or cerebrovascular disease: personal history of myocardial infarction, rhythm disorders or stroke * People wearing a pacemaker or other implanted device, due to the risk of interference * Pregnant or breastfeeding woman * Person working night or shift * Person with a definite plan to move in the coming months (before the second collection during summer) * Person who initially refuses to participate in this second wave of the study * Person working outside the Ile de France

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

General population, no specific condition

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Pierre Louis Institute of Epidemiology and Public Health

    RECRUITING

    Paris, 75012, France