Social outcomes among emerging adults with juvenile idiopathic arthritis
Abstract
This longitudinal study examined social outcomes among young adults with juvenile idiopathic arthritis (JIA) and matched peers during the transition from adolescence to emerging adulthood. Participants included 45 participants with JIA (M = 12.64 years post diagnosis), 46 peers, and their parents. Young adults in both groups were similar on a variety of outcomes, including social self-concept, social competence, family relationships, friendships, and romantic relationships. In general, disease factors were not associated with adjustment. Interventions to assist social functioning may not be necessary for all children with JIA, but additional research is needed to identify potential subgroups at risk for difficulties.
Title of journal, book, etc.
Child Health Care
Date Published
Saturday, January 1, 2011