Solar Lighting to Reduce Indoor Air Pollution in Rural Uganda
Primary Purpose
Pollution; Exposure, Hypertension, Pollution Related Respiratory Disorder
Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Solar lighting system
Sponsored by
About this trial
This is an interventional treatment trial for Pollution; Exposure focused on measuring household air pollution, fine particulate matter, kerosene
Eligibility Criteria
Inclusion Criteria:
- Women living in Nyakabare Parish, Uganda with no prior history of chronic lung disease
Exclusion Criteria:
- Current active tuberculosis in any family member
Sites / Locations
- Massachusetts General Hospital
- Mbarara University of Science and Technology
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Control (usual lighting)
Intervention (solar lighting)
Arm Description
Participants will continue to use their usual lighting sources.
Participants will receive an indoor solar lighting system
Outcomes
Primary Outcome Measures
Fine particulate matter (PM2.5) and Black Carbon
Sampling for PM2.5 and Black Carbon over 48 hours will be collected
Secondary Outcome Measures
Daily use of solar lighting system (hours per day)
A current monitory is installed as part of the solar lighting system that measures the hours per day each light switch is turned on
Blood pressure
Resting blood pressure
Forced Expiratory Volume in one Second (FEV1)
Pre- and Post- bronchodilator spirometry
Heart rate variability
Resting 10 minute heart rate variability
Stool microbiome
Microbial sequencing of the stool will be performed
Qualitative interviews
1:1 qualitative interviews will be performed with participants
Full Information
NCT ID
NCT03351504
First Posted
November 19, 2017
Last Updated
December 5, 2020
Sponsor
Massachusetts General Hospital
Collaborators
Mbarara University of Science and Technology, Harvard School of Public Health (HSPH)
1. Study Identification
Unique Protocol Identification Number
NCT03351504
Brief Title
Solar Lighting to Reduce Indoor Air Pollution in Rural Uganda
Official Title
Solar Lighting Intervention Trial to Reduce Indoor Air Pollution and Improve Adult Respiratory Health in Rural Uganda
Study Type
Interventional
2. Study Status
Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
February 7, 2018 (Actual)
Primary Completion Date
October 31, 2019 (Actual)
Study Completion Date
October 31, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital
Collaborators
Mbarara University of Science and Technology, Harvard School of Public Health (HSPH)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study evaluates the impact of a solar lighting system on kerosene lamp use, levels of indoor air pollution, and health in women living in rural Uganda. Half of the participants will receive the lighting systems immediately, while the other half will receive them after an 18 month delay.
Detailed Description
One fifth of the global population relies on kerosene lamps for lighting, yet few studies have focused on kerosene lighting as a source of indoor air pollution. In our preliminary studies performed in Uganda, we show that homes using solar lighting have much lower levels of indoor air pollution compared to homes using kerosene lighting. The primary goal of this study is to determine the extent to which solar lighting will reduce kerosene use and indoor air pollution in rural Uganda, whether this intervention improves lung health, and to identify the role bacteria in our gut have on determining whether or not people will get sick from indoor air pollution.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pollution; Exposure, Hypertension, Pollution Related Respiratory Disorder
Keywords
household air pollution, fine particulate matter, kerosene
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
Randomization will be performed using dummy codes to represent intervention and control groups by an independent statistician; blinding of the intervention to the participants and field team is not possible, but data analysis will take place prior to unblinding.
Allocation
Randomized
Enrollment
80 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Control (usual lighting)
Arm Type
No Intervention
Arm Description
Participants will continue to use their usual lighting sources.
Arm Title
Intervention (solar lighting)
Arm Type
Experimental
Arm Description
Participants will receive an indoor solar lighting system
Intervention Type
Other
Intervention Name(s)
Solar lighting system
Intervention Description
consisting of a solar panel, rechargeable lead acid battery, charge controller, wiring and switches to 4 lighting points fitted with LED bulbs. This system will include a two-year service warranty.
Primary Outcome Measure Information:
Title
Fine particulate matter (PM2.5) and Black Carbon
Description
Sampling for PM2.5 and Black Carbon over 48 hours will be collected
Time Frame
48 hour
Secondary Outcome Measure Information:
Title
Daily use of solar lighting system (hours per day)
Description
A current monitory is installed as part of the solar lighting system that measures the hours per day each light switch is turned on
Time Frame
baseline, 3 months, 6 months, 12 months after the intervention
Title
Blood pressure
Description
Resting blood pressure
Time Frame
baseline, 3 months, 6 months, 12 months after the intervention
Title
Forced Expiratory Volume in one Second (FEV1)
Description
Pre- and Post- bronchodilator spirometry
Time Frame
baseline, 3 months, 6 months, 12 months after the intervention
Title
Heart rate variability
Description
Resting 10 minute heart rate variability
Time Frame
baseline, 3 months, 6 months, 12 months after the intervention
Title
Stool microbiome
Description
Microbial sequencing of the stool will be performed
Time Frame
baseline, 3 months, 6 months, 12 months after the intervention
Title
Qualitative interviews
Description
1:1 qualitative interviews will be performed with participants
Time Frame
Post-intervention
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Women living in Nyakabare Parish, Uganda with no prior history of chronic lung disease
Exclusion Criteria:
Current active tuberculosis in any family member
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peggy S Lai, MD MPH
Organizational Affiliation
Massachusetts General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States
Facility Name
Mbarara University of Science and Technology
City
Mbarara
Country
Uganda
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
35225388
Citation
Wallach ES, Lam NL, Nuwagira E, Muyanja D, Tayebwa M, Valeri L, Tsai AC, Vallarino J, Allen JG, Lai PS. Effect of a solar lighting intervention on fuel-based lighting use and exposure to household air pollution in rural Uganda: A randomized controlled trial. Indoor Air. 2022 Feb;32(2):e12986. doi: 10.1111/ina.12986.
Results Reference
derived
Learn more about this trial
Solar Lighting to Reduce Indoor Air Pollution in Rural Uganda
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