Hypertension Clinical Trial
Official title:
Solar Lighting Intervention Trial to Reduce Indoor Air Pollution and Improve Adult Respiratory Health in Rural Uganda
Verified date | December 2020 |
Source | Massachusetts General Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 80 |
Est. completion date | October 31, 2020 |
Est. primary completion date | October 31, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 65 Years |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
Uganda | Mbarara University of Science and Technology | Mbarara | |
United States | Massachusetts General Hospital | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Massachusetts General Hospital | Harvard School of Public Health, Mbarara University of Science and Technology |
United States, Uganda,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Fine particulate matter (PM2.5) and Black Carbon | Sampling for PM2.5 and Black Carbon over 48 hours will be collected | 48 hour | |
Secondary | 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 | baseline, 3 months, 6 months, 12 months after the intervention | |
Secondary | Blood pressure | Resting blood pressure | baseline, 3 months, 6 months, 12 months after the intervention | |
Secondary | Forced Expiratory Volume in one Second (FEV1) | Pre- and Post- bronchodilator spirometry | baseline, 3 months, 6 months, 12 months after the intervention | |
Secondary | Heart rate variability | Resting 10 minute heart rate variability | baseline, 3 months, 6 months, 12 months after the intervention | |
Secondary | Stool microbiome | Microbial sequencing of the stool will be performed | baseline, 3 months, 6 months, 12 months after the intervention | |
Secondary | Qualitative interviews | 1:1 qualitative interviews will be performed with participants | Post-intervention |
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