Welcome to the Family Needs Questionnaire – Pediatric Version (FNQ-P)
The Family Needs Questionnaire – Pediatric Version [FNQ-P] is a reliable and valid family-report tool that consists of 40 items representing a range of family needs that may appear after a child or youth sustains an acquired brain injury (ABI). These needs may present across the care continuum (i.e., during acute rehabilitation, post-discharge, or in the community), or over the course of the child’s development. The FNQ-P is suitable for families of children and youth ages 2 to 18 years who have a diagnosed ABI. Clinicians can use the FNQ-P to assess the degree to which the family’s needs have been met across six categories of need: Health Information, Emotional Support, Community Support, Instrumental Support, Professional Support, and Involvement with Care.
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Please note: The BIFI-A Training page is password-protected. Participants attending BIFI-A training must log in to access videos, handouts and reading materials.
