{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["13"],"submitter":["Xu W"],"pubmed_abstract":["<h4>Objective</h4>To investigate the adaptability of Comprehensive Behavioral Intervention for Tics (CBIT) for a Chinese population, and evaluate the efficacy of combined CBIT and pharmacotherapy (CBIT + PT) compared to CBIT or pharmacotherapy (PT) alone for reducing tics and for improving the quality of life (QoL) in a sample of Chinese children with chronic tic disorders (CTD) and Tourette syndrome (TS).<h4>Materials and methods</h4>In this 10-week randomized controlled pilot trial, 37 outpatients aged between 6 and 16 years affected by TS and CTD were randomly assigned to receive CBIT (<i>n</i> = 22) or PT alone (<i>n</i> = 15). Considering the feasibility, the patients allocated to the CBIT treatment group could further choose whether to simultaneously take medicine voluntarily, result"],"journal":["Frontiers in psychiatry"],"pagination":["997174"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9691679"],"repository":["biostudies-literature"],"pubmed_title":["A preliminary study of comprehensive behavioral intervention for tics in Chinese children with chronic tic disorder or Tourette syndrome."],"pmcid":["PMC9691679"],"pubmed_authors":["Jiang W","Ding Q","Han J","Xu W","Zhao Y","Sun J"],"additional_accession":[]},"is_claimable":false,"name":"A preliminary study of comprehensive behavioral intervention for tics in Chinese children with chronic tic disorder or Tourette syndrome.","description":"<h4>Objective</h4>To investigate the adaptability of Comprehensive Behavioral Intervention for Tics (CBIT) for a Chinese population, and evaluate the efficacy of combined CBIT and pharmacotherapy (CBIT + PT) compared to CBIT or pharmacotherapy (PT) alone for reducing tics and for improving the quality of life (QoL) in a sample of Chinese children with chronic tic disorders (CTD) and Tourette syndrome (TS).<h4>Materials and methods</h4>In this 10-week randomized controlled pilot trial, 37 outpatients aged between 6 and 16 years affected by TS and CTD were randomly assigned to receive CBIT (<i>n</i> = 22) or PT alone (<i>n</i> = 15). Considering the feasibility, the patients allocated to the CBIT treatment group could further choose whether to simultaneously take medicine voluntarily, result","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022","modification":"2025-07-13T03:04:10.699Z","creation":"2025-04-19T14:14:08.051Z"},"accession":"S-EPMC9691679","cross_references":{"pubmed":["36440399"],"doi":["10.3389/fpsyt.2022.997174"]}}