Mental health concerns in children with disabilities are common and have a significant and negative impact. Clinicians have reported high demand for this population to receive early, targeted, and family-centred mental health interventions.
We sought to map out and describe existing pediatric mental health services/resources for children with disabilities and their families across clinical sites and local and online communities.
Using a mixed-method triangulation study design, we outreached to clinical managers at the participating clinical sites and conducted a rapid online search of local in-person, telehealth, and web-based information. The nature, access method, admission criteria, target, focus, and other pertinent information were recorded and analyzed using descriptive statistics and a narrative synthesis approach.
Eighty-one ( n = 81) services/resources (in-person, n = 48; telehealth, n = 10; web-based information, n = 33) were identified. Few ( n = 6, 13%) in-person services had a method of care access through an online booking portal. Nearly half of in-person resources ( n = 23, 47%) had admission criteria specific for children with disabilities (e.g., diagnosis, age limit), and many ( n = 32, 67%) required a formal referral. A small number of in-person and telehealth services targeted the mental health concerns of the entire family ( n = 23, 47%; n = 2, 20%). Very few ( n = 13, 16%) services incorporated follow-up support. Important gaps emerged for certain populations (e.g., children with cerebral palsy). Practitioners’ inadequate training when intervening with co-existing mental health demands of children with disabilities was noted by clinical managers.
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