Data collection on children in residential care

Protocol and tools for a national census and survey on children in residential care

A child’s care status impacts his or her health, developmental outcomes and general well-being, both during childhood and later in life. Children outside of a family setting are more likely than their family-based peers to experience abuse, neglect, exploitation, lack of stimulation, poor nutrition and toxic stress, with lifelong physical and psychological repercussions. Moreover, children living in institutional settings are frequently missing from official statistics since reporting for many indicators, particularly those that comprise global monitoring frameworks such as the Sustainable Development Goals (SDGs), rely heavily on data collected through household surveys.

In response to the need for accurate and reliable statistics on children in residential care, UNICEF has developed the first-ever comprehensive package to collect data on children living in residential care settings. It is comprised of a protocol that outlines the recommended steps for gathering the data; 12 data collection tools; and a comprehensive implementation package covering all aspects from design to dissemination of the findings.

These objectives are achieved through two phases of data collection: Phase 1 is the census of facilities and enumeration of children and Phase 2 is the follow-up survey on selected measures of well-being for a representative sample of children living in residential care.

Available documentation currently includes a concept note  and a webinar recording. The full protocol and package of implementation tools are currently been finalized and will be posted online as they become available.