Resiliency Intervention for Siblings of Children With Autism Spectrum Disorder: A Randomized Pilot Trial

被引:3
作者
Kuhlthau, Karen A. [1 ,2 ,7 ]
Traeger, Lara [3 ,4 ,5 ]
Luberto, Christina M. [3 ,4 ,5 ,6 ]
Perez, Giselle K. [3 ,4 ,5 ,6 ]
Goshe, Brett M. [3 ,6 ]
Fell, Lucy [1 ]
Iannuzzi, Dorothea [1 ]
Park, Elyse R. [3 ,4 ,5 ,6 ]
机构
[1] Massachusetts Gen Hosp Children, Dept Pediat, Div Gen Acad Pediat, Boston, MA USA
[2] Harvard Med Sch, Dept Pediat, Boston, MA USA
[3] Harvard Med Sch, Massachusetts Gen Hosp, Dept Neurol, Boston, MA USA
[4] Massachusetts Gen Hosp, Dept Psychiat, Hlth Promot & Resiliency Intervent Res Program, Boston, MA 02114 USA
[5] Massachusetts Gen Hosp, Dept Med, Hlth Promot & Resiliency Intervent Res Program, Boston, MA USA
[6] MGH Benson Henry Inst Mind Body Med, Boston, MA USA
[7] Massachusetts Gen Hosp, 125 Nashua St 860, Boston, MA 02114 USA
关键词
Autism; Sibling; Resiliency; VALIDATION; ADJUSTMENT; PROGRAM; HEALTH;
D O I
10.1016/j.acap.2022.11.011
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BACKGROUND /OBJECTIVES: Neurotypical siblings (NT sib-lings) of children with autism spectrum disorder (ASD) are at elevated risk for emotional distress and adjustment problems. Resiliency is the ability to cope and adapt with ongoing stressors. We conducted a randomized waitlist-controlled pilot trial to examine the feasibility, acceptability, and preliminary efficacy of an adapted virtual mind-body resiliency group intervention for teen NT siblings of children with ASD.METHODS: We modified the Stress Management and Resiliency Training-Relaxation Response Resiliency Program for NT siblings of children with ASD (SibChat). We randomly assigned teens (aged 14-17) to immediate intervention (IG) versus waitlist control (WLC). The intervention included eight 60-minute weekly video conference group sessions. We assessed feasibility (enrollment, attendance, and retention) and acceptability (post treatment survey and weekly relaxation response practice). We explored group differences in pre-post change scores for 1) stress coping (Measure of Current Status-A) and 2) resiliency (Current Experiences Scale) using independent samples t tests and effect size calculations.RESULTS: We enrolled 83% of screened eligible teens. A total of 90% IG and 75% WLC participants attended at least 6/8 sessions. Among IG participants who completed the post treatment survey, 79% reported practicing relaxation response exercises at least "a few times a week". Comparing change in baseline to time 1, the IG showed better relative changes than the WLC group in stress coping (d = 0.60) and resiliency (d = 0.24).CONCLUSIONS: Our pilot trial showed promising feasibility, acceptability, and preliminary efficacy of SibChat on at least one of the 2 primary outcomes supporting further testing of the SibChat intervention.CLINICAL TRIAL REGISTRATION: US National Library of Medicine. Registration number: NCT04369417. https://clinical trials.gov/ct2/show/NCT04369417.
引用
收藏
页码:1187 / 1195
页数:9
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