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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.

Authors :
Lee, Sun Haeng
Shin, Seungwon
Kim, Tae-hun
Kim, Sang Min
Do, Tae Yoon
Park, Sulgi
Lee, Boram
Shin, Hye Jin
Lee, Jihong
Lee, Jin Yong
Chang, Gyu Tae
Source :
Trials. 7/15/2019, Vol. 20 Issue 1, pN.PAG-N.PAG. 1p. 1 Diagram, 3 Charts.
Publication Year :
2019

Abstract

<bold>Background: </bold>Autism 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.<bold>Methods/design: </bold>This 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: 1. A UGSJB granule with acupuncture, twice daily (n = 120) 2. 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 24 weeks 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.<bold>Discussion: </bold>We 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.<bold>Trial Registration: </bold>Clinical Research Information Service: KCT0003007 (registered on April 5, 2018). [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17456215
Volume :
20
Issue :
1
Database :
Academic Search Index
Journal :
Trials
Publication Type :
Academic Journal
Accession number :
137490002
Full Text :
https://doi.org/10.1186/s13063-019-3537-7