Electric Kettle Promotion: Provision of free electric kettles and promotional materials/information
Study summary
This study will evaluate the impact of a pilot Rural Electric Kettle Promotion Program offered to low-income households in rural Anhui Province, China. The primary objective of this study is to determine whether this promotion program causes poverty households currently boiling their drinking water with solid-fuels (or drinking untreated water or bottled water) to switch to boiling their drinking water with electric kettles, and if so, how such a switch might improve safe drinking water access and/or reduce household air pollution.
Eligibility
Sex
ALL
Min age
—
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria:
* Persons aged 18 or older will be eligible to provide consent for their households.
* Government classified "poverty households" (poverty classification based on 2016 data/records).
Exclusion Criteria:
* Persons aged 17 or younger will not be eligible to provide consent for their households.
* We will not have any exclusion criterion based on gender, race, ethnicity, language, or literacy.
Primary outcome measure(s)
Change in proportion of households using electric kettles for boiling drinking water — 24 months. Primary measurement via electricity use meters (Tepsung model 10/16A) affixed to electric kettle power cables for all household who report using electric kettles at each of five visits (based on total KWh consumed per data collection intervals and estimated mean liters boiled per person, per day, per household, by electric kettle type/size). Additional measurement via self-report of electric kettle use (household surveys) and via enumerator direct observations (during visits to households).
Trial sites (1)
Facility
City
Region
Status
National Center for Rural Water Supply Technical Guidance,Chinese Center for Disease Control and Prevention
Beijing
China
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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