Heat Stress Exposure Among Low-Income Residents in Bangladesh and Evaluation of Indoor Interventions

ConditionHeat Stress
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorUniversity of California, Berkeley

About this trial

The goal of this clinical trial is to learn if infrastructure and equipment installed to cool homes reduce adverse health outcomes. The main questions it aims to answer are:

What is the impact of the intervention on indoor heat stress? What is the impact of the intervention on personal exposure to heat stress? What is the impact of the intervention on health outcomes, including heart rate, and heart rate variability, and sleep quality?

Participants will have cooling infrastructure and/or equipment installed in their home; have heat stress sensors installed inside and outside their home and wear personal heat stress monitors; allow some biological functions such as heat rate, heat rate variability, and sleep quality.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

House is located in an informal settlement in an urban area in Bangladesh

The house has a corrugated iron roof and corrugated iron walls

The household plans to remain in the house from Feb-Nov

Disqualifiers

There is an inhabited structure about the house

The landlord does not allow the proposed intervention

Lives in an eligible household

Has access to air conditioning in their home or place of work

Trial design

Design model

Single group

Treatments tested in this trial

  • Cooling intervention

    Other intervention

    Infrastructure and/or equipment that cools the house in the hot season

Treatment groups

1,539 Participants
are divided into 2 treatment groups
Group A: Indoor cooling interventionExperimental treatment 1 intervention
Group B: ControlNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Heart rate

resting heart rate (beats per minute, bpm), where lower heart rate is better

Time frame
0, 2, and 4 weeks

Secondary outcomes

1

Heart rate variability

resting heart rate (beats per minute, bpm) variability, where higher variability is better

Time frame
0, 2, and 4 weeks
2

Sleep quality

Self-reported sleep quality and number of minutes in rapid eye movement (REM), as recorded by a fitness watch, where more time in REM is better

Time frame
0, 2, and 4 weeks
3

Irritability

Self-reported irritability, as measured by the Brief Irritability Test (BITe), where a lower score is better

Time frame
0, 2, and 4 weeks
4

Environmental Symptoms

Environmental symptoms, as measured by the abbreviated environmental symptoms questionnaire, where a lower score is better

Time frame
0, 2, and 4 weeks

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of California, Berkeley

Lead sponsor

National Institute of Environmental Health Sciences (NIEHS)

Collaborator