Efficacy of Hippotherapy Versus Pharmacotherapy in Attention-Deficit/Hyperactivity Disorder: A Randomized Clinical Trial

CBCL公司 医学 药物治疗 注意缺陷多动障碍 生活质量(医疗保健) 社会心理的 评定量表 随机对照试验 临床全球印象 冲动性 精神科 临床试验 物理疗法 儿科 临床心理学 安慰剂 心理学 内科学 替代医学 护理部 病理 发展心理学
作者
Yunhye Oh,Yoo‐Sook Joung,Byongsu Jang,Jae Hyun Yoo,Jihye Song,Jiwon Kim,Ki-Ho Kim,Seonwoo Kim,Ji-Young Lee,Hye-Yeon Shin,Jeong‐Yi Kwon,Yun‐Hee Kim,Bumseok Jeong
出处
期刊:Journal of Alternative and Complementary Medicine [Mary Ann Liebert, Inc.]
卷期号:24 (5): 463-471 被引量:58
标识
DOI:10.1089/acm.2017.0358
摘要

OBJECTIVES: Pharmacotherapy among children with attention-deficit/hyperactivity disorder (ADHD) is effective, but many patients suffer from secondary psychiatric problems even after improvement of ADHD core symptoms. Hippotherapy have been used as adjunct treatment options for physical and psychosocial rehabilitation as well as to ameliorate core symptoms. The aim of this study was to investigate the effects of Hippotherapy versus pharmacotherapy for children with ADHD. DESIGN: Thirty-four participants with ADHD were randomly assigned at a 1:1 ratio to either 24 sessions of a twice-weekly hippotherapy or pharmacotherapy. To assess therapeutic effects, the ADHD Rating Scale (ARS) was used pretreatment and posttreatment as the primary outcome measure. Secondary outcomes included the Child Behavior Checklist (CBCL), Self-Esteem Scale (SES), Pediatric Quality of Life Inventory (PedsQL) child and parent report version, Developmental Coordination Disorder Questionnaire (DCDQ), Clinical Global Impressions-Severity (CGI-S), and quantitative electroencephalography. RESULTS: Both groups showed marked improvements in ADHD symptoms, CGI-S. No significant differences between groups were detected regarding treatment outcome except thought problem subscales of CBCL. Twelve weeks of hippotherapy improved attention, impulsivity/hyperactivity, and quality of life. CONCLUSION: This trial is promising, but further studies are required to evaluate the long-term clinical effectiveness of hippotherapy. The study is registered with ClinicalTrials.gov, number NCT 02482649.
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