Optimizing Ventilation to Improve Health

October 7, 2022 updated by: Stephen P Luby, Stanford University

Optimizing Windows to Improve Ventilation in Dhaka Slums

Our overall goal is to optimize preferred, ventilating windows/apertures/vents in low-income neighborhoods of Dhaka, Bangladesh. We will:

I. Collect baseline data on housing types and finalize windows/vents protoypes.

II. Measure the impact of improved ventilation on air exchange rates in houses in low-income neighborhoods of Dhaka and characterize the current and potential market for windows/vents in households in low-income neighborhoods of Dhaka, Bangladesh.

III. Understand recipients' (tenants and landords) perceived benefits of installed window/vent designs and difficulties faced with adoption of each design

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

240

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Dhaka, Bangladesh, 1212
        • International Centre for Diarrhoeal Disease Research, Bangladesh

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • 1) lack cross-ventilation at the time of enrollment
  • 2) have obtained landlord permission to make adjustments to their dwelling,
  • 3) have a free roof where a window can be installed

Exclusion Criteria:

  • 1) Household reports receiving dust from nearby machine that pulverizes materials for making roads

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Part 1. Focus group discussions on ventilation preferences
Participant's perceived benefits/detriments of having ventilation options in the household and their opinions on the behavior change material developed to encourage increased household ventilation will be explored using 6-9 focus group discussions with 10-12 participants each.
No Intervention: Part 2. PM 2.5 pilot
Indoor, outdoor, and personal particulate matter concentrations among ten mother-child pairs and their homes will be monitored.
Experimental: Part 3. Intervention
Households will participate in a baseline survey and a Beck-DeGroot-Marshak auction to establish willingness-to-pay for ventilation. If the household wins, or if it is decided to install ventilation in all intervention households, the household will receive installation of a ventilating mechanism.
The intervention is installation of a ventilating structure, in this case a window in the house roof.
No Intervention: Part 3. Control
For 12 month after intervention, the air exchange rate will be measured in all control households.
No Intervention: Part 4. Spillover
Households that neighbor enrolled study households will be surveyed and asked whether they, on their own, chose to install a window. If they did install a window, they will be asked how much they paid.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Household air exchange rate - spring (Part 3)
Time Frame: 50 minutes
Repeated household measurements of effective point ventilation to approximate air exchange rates in both treatment and control households will be obtained. Air exchange rates will be reported as air changes per hour for the home as well as liters of air per cubic meter per second per person.
50 minutes
Household air exchange rate - summer (Part 3)
Time Frame: 50 minutes
Repeated household measurements of effective point ventilation to approximate air exchange rates in both treatment and control households will be obtained. Air exchange rates will be reported as air changes per hour for the home as well as liters of air per cubic meter per second per person.
50 minutes
Household air exchange rate - fall (Part 3)
Time Frame: 50 minutes
Repeated household measurements of effective point ventilation to approximate air exchange rates in both treatment and control households will be obtained. Air exchange rates will be reported as air changes per hour for the home as well as liters of air per cubic meter per second per person.
50 minutes
Household air exchange rate - winter (Part 3)
Time Frame: 50 minutes
Repeated household measurements of effective point ventilation to approximate air exchange rates in both treatment and control households will be obtained. Air exchange rates will be reported as air changes per hour for the home as well as liters of air per cubic meter per second per person.
50 minutes
Number of households that adopt the intervention (Part 3)
Time Frame: 20 minutes
Takeup of the intervention will be defined by whether a household had a ventilation design installed, either by winning the BDM auction paying the full price or by accepting a free installation after previously losing the BDM auction.
20 minutes
Revealed willingness-to-pay for ventilation (Part 3)
Time Frame: 20 minutes
We will obtain stated willingness-to-pay for the ventilation designs through the BDM auction mechanism, which will be used to trace out a demand curve for ventilation, plotting the number of households that are willing to pay for a window agaist their stated price.
20 minutes
Concentration of radon gas in house (Part 3)
Time Frame: 7 days
We will assess the concentration gas in a subset of study households.
7 days
Concentration of indoor particulate matter 2.5 (Part 3)
Time Frame: 48 hours for normal tests; 72 hours for quality control tests.
We will determine the indoor PM2.5 levels in study households, as well as the number of hours with indoor PM2.5 exceeding 50 and 100 µg/m3 during the observation period. A subset of households will have longer tests for quality control.
48 hours for normal tests; 72 hours for quality control tests.
Concentration of indoor particulate matter 2.5 (Part 2)
Time Frame: up to 5 hours
We will determine the indoor PM2.5 levels in study households, as well as the number of hours with indoor PM2.5 exceeding 50 and 100 µg/m3 during the observation period.
up to 5 hours
Concentration of outdoor particulate matter 2.5 (Part 2)
Time Frame: up to 5 hours
We will determine the outdoor PM2.5 levels near the study households.
up to 5 hours
Personal exposure to particulate matter 2.5 - mother (Part 2)
Time Frame: up to 5 hours
We will determine the PM2.5 levels near the mother using a monitor worn on her body.
up to 5 hours
Personal exposure to particulate matter 2.5 - child (Part 2)
Time Frame: up to 5 hours
We will determine the PM2.5 levels near the child using a monitor worn on her body.
up to 5 hours
Number of non-study, neighboring households that adopt the intervention and their willingness to pay (Part 4)
Time Frame: 15 minutes
We will survey households that neighbor enrolled study households to ask if they have installed a window on their own since the enrollment for the randomized control trial. If they did install a window, we will ask how much they paid.
15 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Stephen P Luby, Dr., Stanford University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 19, 2018

Primary Completion (Actual)

November 1, 2021

Study Completion (Actual)

June 30, 2022

Study Registration Dates

First Submitted

March 27, 2019

First Submitted That Met QC Criteria

March 27, 2019

First Posted (Actual)

March 29, 2019

Study Record Updates

Last Update Posted (Actual)

October 12, 2022

Last Update Submitted That Met QC Criteria

October 7, 2022

Last Verified

October 1, 2022

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 46212

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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