ClinicalTrials.gg
RecruitingNCT06982339Updated Jan 22, 2026

Beat the Heat Boston

An interventional study of Air Conditioner and Electricity subsidy in Hot Weather; Adverse Effect, Heat Effect and Heat Stress, sponsored by Harvard School of Public Health (HSPH). Recruiting at 1 site in United States. Open to participants aged 55 Years to 95 Years. Per ClinicalTrials.gov, last updated 2026-01-22.

Primary conditionHeat StrokeRegistry: Heat Stress DisordersReclassifiedWhy we changed it
Registry
Heat Stress Disorders — the first condition term the registry derived for this study.
ClinicalTrials.gg
Heat Stroke
Why
  1. The study's listed conditions name Heat Stroke, a narrower term within Heat Stress Disorders.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Harvard School of Public Health (HSPH) · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Started May 2025; still recruiting 1 year 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
55 Years to 95 Years
Sex
All
01

Study summary

The goal of this stepped wedge trial is to assess the practical effects of air conditioners on hot weather impacts among older adults. The main questions it aims to answer are:

How does the presence of an air conditioning unit affect heat stress, heat strain, mental health, and healthcare utilization among older adults who did not previously have access to air conditioning?

How, and in what conditioners, do older adults use air conditioning once it is installed in their home?

Researchers will compare participants in arms with (A) and without (B) air conditioning units in the first summer season; this will allow them to assess the effect of air conditioners. In the second summer season, both arms will have air conditioning units, but those in the year two distribution arm (B) will receive an electricity subsidy, while those in the year one AC distribution arm (A) will not, allowing researchers to assess the effect of an electricity subsidy.

Participants will be randomized to receive an air conditioner and financial support for electricity costs in either the first summer season or the second summer season of the study.

  • Heat stress, heat strain, mental health, and healthcare utilization will be assessed via participant survey.
  • Air conditioner utilization will be assessed via continuous load monitoring devices.
  • Indoor air temperature will be assessed via continuous data loggers.
Read the detailed description

This community-based, randomized stepped wedge trial investigates whether the provision of educational resources and air conditioning (AC) improves thermal comfort and health outcomes among older adults with chronic disease and material hardships. The study will enroll 100 participants residing in at risk neighborhoods. Eligibility criteria include adults aged 55-95 who speak English or Spanish, lack access to home cooling systems, and have at least one qualifying chronic health condition or a history of recent hospitalization (see Eligibility section) .

Participants will be randomly assigned (1:1) to receive window AC units and an electricity cost subsidy either in Year 1 or Year 2. All participants in both arms will receive a baseline intervention including heat health educational materials and cooling kits. Data collection will occur over two warm seasons (April-September) and involve pre- and post-intervention assessments using structured surveys, real-time environmental monitoring, and AC usage tracking.

Surveys administered at enrollment and in late summer each year will capture a broad range of covariates including sociodemographic data, housing conditions, health service utilization, self-reported symptoms, and adaptive behaviors. Heat stress, heat strain, mental health, and healthcare utilization outcomes will be assessed via surveys that include previously validated survey instruments. Specific emphasis will be placed on measures of energy insecurity, such as utility shutoff notices, receipt of energy assistance, and trade-offs between essential expenses. Environmental sensors will log indoor temperature, humidity, and pollutant data throughout the study period.

The primary outcome is self-reported health status as measured by a modified ESQ-IV, supplemented by secondary metrics including ASHRAE thermal comfort scores, POMS, emergency department presentations, and hospitalizations. Statistical analysis will employ two-sample t-tests to detect treatment effects, with a minimum detectable effect size of 5.66 assuming a standard deviation of 10 and balanced sample sizes.

This study aims to empirically quantify the health benefits of cooling interventions in high-risk older adults and inform scalable public health strategies that address the intersecting challenges of urban heat, chronic disease management, and housing-related inequities.

02

Conditions studied

  • Hot Weather; Adverse Effect
  • Heat Effect
  • Heat Stress
  • Heat Stroke, Heat Exhaustion
  • Heat Exposure
  • Heat Strain

Browse trials for

Keywords

  • Cooling
  • Air conditioner
  • Heat related illness
  • stepped wedge
03

In context

Heat Stroke Reclassified

21 studies on the registry are indexed under Heat Stroke; 10 are open to participants now.

This study's planned enrollment of 100 is above the median of 34 across 13 interventional studies indexed under Heat Stroke.

Browse Heat Stroke studies →

Lead sponsor

Harvard School of Public Health (HSPH) is the lead sponsor of 154 studies on the registry; 10 are open to participants now.

Compared within Heat Stroke, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Heat Stress Disorders. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
55 Years to 95 Years
Sexes eligible
All
Accepts healthy volunteers
No

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.

Inclusion criteria

  • reside in Roxbury, Dorchester, East Boston or Mattapan MA
  • age 55-95 years old
  • speak English or Spanish
  • do not have air conditioning in the home
  • living with at least one of the following conditions: chronic CVD (hypertension, hyperlipidemia, diabetes, history of stroke or myocardial infarction, atrial fibrillation, or heart failure), chronic pulmonary disease (asthma, /emphysema, interstitial lung disease), chronic neurologic disease (stroke, Parkinson's disease, or other chronic neurologic conditions), chronic mental health conditions (including anxiety disorder, major depression, bipolar disorder), and/or history of hospitalization (defined as spending at least one night in the hospital) for any reason within the past three years.

Exclusion criteria

Exclusion Criteria:

- Lack a location in their home suitable for installation of the AC unit provided during the research study.

Terms in these criteria, in plain language(1)

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.

COPD

Chronic obstructive pulmonary disease: long-term lung disease that makes it hard to breathe out, including emphysema and chronic bronchitis.

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    Early Air Conditioning

    Year 1: Participants receive a window AC unit and a financial subsidy for electricity. Year 2: Participants continue to have their AC unit, but do not receive a financial subsidy for electricity.

    Other: Air Conditioner · Other: Electricity subsidy

  • No intervention
    Delayed Air Conditioning

    Year 1: No intervention. Year 2: Participants receive an AC unit along with a financial subsidy for electricity.

Interventions

  • OtherAir Conditioner

    Air conditioners will be window-mounted units powered by 110v AC.

  • OtherElectricity subsidy

    Electricity subsidies will consist of a single block subsidy of USD 100, intended to provide support for the electricity costs associated with operating an air conditioning unit.

06

What researchers measure

Primary outcomes

  1. Environmental Symptoms Questionnaire (ESQ-IV)

    The primary outcome will be a two-sample t-test for differences in means in the treatment and control groups in responses to the Environmental Symptoms Questionnaire (ESQ-IV). We will assess self-reported health impacts across all sites using a modified (truncated) version of the Environmental Symptoms Questionnaire (ESQ-IV), referred to as the Heat Stress Symptoms Questionnaire. Originally developed for assessing the health impacts of environmental exposures (Sampson et al, 1993), the ESQ-IV has been validated for assessing health impacts associated with heat illness in soldiers (Johnson \& Merullo, 1993). More recently, smaller subsets of the ESQ-IV's questions have served as a health endpoint for assessing the impacts of heat stress and acclimatization in the general population and older adults (McGarr et al, 2023; Manning et al, 2023). In an urban population, a question using similar language in a simplified format was used to assess prior experiences of heat-related illness (Card

    Time frame: Difference in self-reported symptoms on HSSQ administered in the late summer season, 2-12 weeks after enrollment.

Secondary outcomes

  1. Air Conditioner Utilization

    Air conditioner utilization will be prospectively assessed throughout the study. In year 1, air conditioner utilization will be analyzed in relation to indoor air temperature to identify threshold temperatures that trigger AC utilization. In Year 2, utilization rates and thresholds will be compared between the the two arms to assess the impact of electricity subsidies on AC utilization.

    Time frame: From enrollment to study completion, approximately 2 years.

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Yes — Non-identifiable study dataset, specifically data on treatment arm assignment and survey results including primary endpoint

Supporting information: Study protocol, Statistical analysis plan, Informed consent form

Time frame: Data will be made available at the time of publication of study results.

Access criteria: Data will be available upon reasonable request.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started May 2025 (actual). Primary completion is estimated for Oct 2026, 16 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
May 13, 2025
First posted
May 21, 2025
StartActual
May 19, 2025
Primary completionEst.
Oct 15, 2026
CompletionEst.
Oct 15, 2026
Last update
Jan 22, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jan 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06982339
Responsible party
Gary Adamkiewicz (Associate Professor of Environmental Health and Exposure Disparities, Harvard School of Public Health (HSPH)) — Principal investigator
First posted
May 21, 2025
Start date
May 19, 2025
Primary completion
Oct 15, 2026 (estimated)
Completion
Oct 15, 2026 (estimated)
Last update
Jan 22, 2026

Study contacts

Caleb Dresser Assistant Professor in Environmental Health, MD MPH
Contact
beattheheatboston@gmail.com
(617) 446-3248
Gary Adamkiewicz Associate Professor of Environmental Health and Exposure Disp., PhD, MPH, MS
principal investigator · Harvard School of Public Health (HSPH)

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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