Solar Lighting to Reduce Indoor Air Pollution in Rural Uganda
- Conditions
- Pollution; ExposurePollution Related Respiratory DisorderHypertension
- 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
- Women living in Nyakabare Parish, Uganda with no prior history of chronic lung disease
- Current active tuberculosis in any family member
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Intervention (solar lighting) Solar lighting system Participants will receive an indoor solar lighting system
- Primary Outcome Measures
Name Time Method Fine particulate matter (PM2.5) and Black Carbon 48 hour Sampling for PM2.5 and Black Carbon over 48 hours will be collected
- Secondary Outcome Measures
Name Time Method 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 pressure baseline, 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 variability baseline, 3 months, 6 months, 12 months after the intervention Resting 10 minute heart rate variability
Stool microbiome baseline, 3 months, 6 months, 12 months after the intervention Microbial sequencing of the stool will be performed
Qualitative interviews Post-intervention 1:1 qualitative interviews will be performed with participants
Respiratory symptoms baseline, 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
πΊπΈBoston, Massachusetts, United States
Mbarara University of Science and Technology
πΊπ¬Mbarara, Uganda