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Solar Lighting to Reduce Indoor Air Pollution in Rural Uganda

Not Applicable
Completed
Conditions
Pollution; Exposure
Pollution Related Respiratory Disorder
Hypertension
Interventions
Other: Solar lighting system
Registration Number
NCT03351504
Lead Sponsor
Massachusetts General Hospital
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
80
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention (solar lighting)Solar lighting systemParticipants will receive an indoor solar lighting system
Primary Outcome Measures
NameTimeMethod
Fine particulate matter (PM2.5) and Black Carbon48 hour

Sampling for PM2.5 and Black Carbon over 48 hours will be collected

Secondary Outcome Measures
NameTimeMethod
Daily use of solar lighting system (hours per day)baseline, 3 months, 6 months, 12 months after the intervention

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 pressurebaseline, 3 months, 6 months, 12 months after the intervention

Resting blood pressure

Forced Expiratory Volume in one Second (FEV1)baseline, 3 months, 6 months, 12 months after the intervention

Pre- and Post- bronchodilator spirometry

Heart rate variabilitybaseline, 3 months, 6 months, 12 months after the intervention

Resting 10 minute heart rate variability

Stool microbiomebaseline, 3 months, 6 months, 12 months after the intervention

Microbial sequencing of the stool will be performed

Qualitative interviewsPost-intervention

1:1 qualitative interviews will be performed with participants

Respiratory symptomsbaseline, 3 months, 6 months, 12 months after intervention

Presence/absence of respiratory symptoms based on the American Thoracic Society Respiratory Disease questionnaire

Trial Locations

Locations (2)

Massachusetts General Hospital

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Boston, Massachusetts, United States

Mbarara University of Science and Technology

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Mbarara, Uganda

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