Safety, effectiveness, and economic evaluation of an herbal medicine, Ukgansangajinpibanha granule, in children with autism spectrum disorder: a study protocol for a prospective, multicenter, randomized, double-blinded, placebo-controlled, parallel-group clinical trial

被引:6
|
作者
Lee, Sun Haeng [1 ,2 ]
Shin, Seungwon [3 ]
Kim, Tae-hun [4 ]
Kim, Sang Min [1 ]
Do, Tae Yoon [1 ,2 ]
Park, Sulgi [1 ,2 ]
Lee, Boram [1 ]
Shin, Hye Jin [1 ,5 ]
Lee, Jihong [1 ,5 ]
Lee, Jin Yong [1 ,2 ]
Chang, Gyu Tae [1 ,5 ]
机构
[1] Kyung Hee Univ, Dept Clin Korean Med, Grad Sch, 26 Kyungheedae Ro, Seoul 02447, South Korea
[2] Kyung Hee Univ, Dept Pediat Korean Med, Korean Med Hosp, Med Ctr, 23 Kyungheedae Ro, Seoul 02447, South Korea
[3] Kyung Hee Univ, Dept Korean Med, 26 Kyungheedae Ro, Seoul 02447, South Korea
[4] Kyung Hee Univ, Korean Med Clin Trial Ctr, Korean Med Hosp, Med Ctr, 23 Kyungheedae Ro, Seoul 02447, South Korea
[5] Kyung Hee Univ Hosp Gangdong, Dept Pediat Korean Med, 892 Dongnam Ro, Seoul 05278, South Korea
关键词
Herbal medicine; Acupuncture; Autism spectrum disorder; Randomized controlled trial; Ukgansangajinpibanha; BEHAVIOR CHECKLIST; RELIABILITY; YOKUKANSAN; SYMPTOMS; VALIDITY; ADOLESCENTS; PREVALENCE; CONSTRUCT; NETWORK;
D O I
10.1186/s13063-019-3537-7
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundAutism spectrum disorder (ASD) is characterized by continuous impairment in communication and social interaction and by limited and repetitive behaviors, interests, or activities. Behavioral, educational, and pharmaceutical interventions have been shown to reduce behavioral disabilities, improve verbal/non-verbal communication, and help patients acquire self-reliance skills. However, there has been a lack of systematic verification and consensus regarding the treatment of the core symptoms of ASD because of its unclear etiology. Ukgansangajinpibanha (UGSJB), a legitimately prescribed herbal medicine for nervousness, insomnia, night crying, and malnutrition in South Korea and Japan, has been used for angry, sensitive, nervous, and unsettled children with ASD.Methods/designThis trial is a prospective, multicenter, randomized, double-blinded, placebo-controlled, parallel-group, clinical trial. The 4- to 6-year-old children with ASD will be randomly assigned to following groups: A UGSJB granule with acupuncture, twice daily (n=120)A placebo group with acupuncture, twice daily (n=120).The following outcome measures will be used: behavior by the Childhood Autism Rating Scale, Autism Behavior Checklist, and Aberrant Behavior Checklist; social maturity by the Social Maturity Scale; quality of life by the Child Health Questionnaire and EuroQoL Five-dimension Five-level Youth; and parental stress by the Parenting Stress Index at baseline and at 6, 12, and 24weeks after the beginning of treatment.In addition, to evaluate safety, we will investigate the adverse reactions that may be caused by UGSJB granule. Finally, we will make an economic evaluation of UGSJB for the treatment of ASD.DiscussionWe prepared a well-designed clinical trial to investigate the safety and effectiveness of UGSJB on ASD symptoms compared with placebo treatment. The results from this study will provide clinical evidence on the safety, effectiveness, and economic value of UGSJB combined with acupuncture in children with ASD.Trial registrationClinical Research Information Service: KCT0003007 (registered on April 5, 2018)
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页数:11
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