Table 1.

Primary and secondary outcome measures at 6 and 12 months post injury.

Outcomes		Participants	Description	Completed by
Primary outcomes
	Rehabilitation Complexity Scale Extended–Trauma (RCS E–Trauma) [31]	Adult/child	Estimation of specialized inpatient rehabilitation needs	Rehabilitation specialist
	Needs and Provision Complexity Scale (NPCS) A (Needs) and B (Gets) [27]	Adult/child	Estimation of community-based rehabilitation needs and registration of community-based rehabilitation provided (Gets)	Clinician version: rehabilitation specialist Patient version: patients by interview
	Family Needs Questionnaire–Pediatric Version (FNQ-P) [32]	Families of children and youth	A measure for assessing the degree to which the family’s needs have been met	Caregivers for children 2-18 years
Secondary outcomes
	Glasgow Outcome Scale Extended (GOSE) [33]	Adult/child	A global outcome commonly used in trauma research	Clinician
	Resilience Scale for Adults (RSA) [34]	Adult	A measure of resilience	Patients
	Patient Health Questionnaire 9 (PHQ-9) [35]	Adult	A screening of depression	Patients
	Generalized Anxiety Disorder 7 (GAD-7) [36]	Adult	A screening of anxiety	Patients
	Impact of Event Scale–Revised (IES-R) [37]	Adult	A measure of presence of subjective distress in adults	Patients
	Children’s Revised Impact of Event Scale (CRIES-8) [38]	Child/parent	A measure of subjective distress in pediatric cases	Children from 8 years of age; caregivers
	Strengths and Difficulties Questionnaire (SDQ) [39]	Child	A brief behavioral measure (4-17 years)	Caregivers for children 4-17 years Children 11-17 years
	Return to work/school	Adult/family caregiver/ child/parent	Work/school status, return to same role/position, benefits from the labor welfare system at individual and family levels	Clinicians by interview
	WHOa Disability Assessment Schedule 2.0 (WHODAS 2.0) [40]	Adult	A measure of functioning and disability: cognition, mobility, self-care, getting along, life activities and participation	Patients/caregivers
	EuroQol Questionnaire (EQ-5D) [41]	Adult/family caregiver/ child/parent	A generic measure of health status (mobility, self-care, usual activities, pain/discomfort, anxiety/depression); health profiles and a weighted total value for HRQL	Patients/caregivers Parent proxy for children 0-15 years Children: 8-15 years
	Pediatric Quality of Life Inventory (Peds-QL) 4.0 Generic Core Scales [42]	Child/parent	Patient’s and parent’s perceptions of quality of life	Parents: parent proxy for toddlers (2-4 years), young children (5-7 years), children (8-12 years), and teens (13-18 years) Children/teens: self-report for 5-7 years, 8-12 years, and teens (13-18 years)

^aWHO: World Health Organization.