| Literature DB >> 34313861 |
Per Andrén1, Ewgeni Jakubovski2, Tara L Murphy3, Katrin Woitecki4, Zsanett Tarnok5, Sharon Zimmerman-Brenner6, Jolande van de Griendt7, Nanette Mol Debes8, Paula Viefhaus4, Sally Robinson9, Veit Roessner10, Christos Ganos11, Natalia Szejko12,13,14, Kirsten R Müller-Vahl2, Danielle Cath15, Andreas Hartmann16, Cara Verdellen17.
Abstract
Part II of the European clinical guidelines for Tourette syndrome and other tic disorders (ECAP journal, 2011) provides updated information and recommendations for psychological interventions for individuals with tic disorders, created by a working group of the European Society for the Study of Tourette Syndrome (ESSTS). A systematic literature search was conducted to obtain original studies of psychological interventions for tic disorders, published since the initial European clinical guidelines were issued. Relevant studies were identified using computerized searches of the MEDLINE and PsycINFO databases for the years 2011-2019 and a manual search for the years 2019-2021. Based on clinical consensus, psychoeducation is recommended as an initial intervention regardless of symptom severity. According to a systematic literature search, most evidence was found for Habit Reversal Training (HRT), primarily the expanded package Comprehensive Behavioral Intervention for Tics (CBIT). Evidence was also found for Exposure and Response Prevention (ERP), but to a lesser degree of certainty than HRT/CBIT due to fewer studies. Currently, cognitive interventions and third-wave interventions are not recommended as stand-alone treatments for tic disorders. Several novel treatment delivery formats are currently being evaluated, of which videoconference delivery of HRT/CBIT has the most evidence to date. To summarize, when psychoeducation alone is insufficient, both HRT/CBIT and ERP are recommended as first-line interventions for tic disorders. As part of the development of the clinical guidelines, a survey is reported from ESSTS members and other tic disorder experts on preference, use and availability of psychological interventions for tic disorders.Entities:
Keywords: Behavior therapy; Comprehensive behavioral intervention for tics; Exposure and response prevention; Habit reversal training; Tic disorders; Tourette syndrome; Treatment guidelines
Mesh:
Year: 2021 PMID: 34313861 PMCID: PMC8314030 DOI: 10.1007/s00787-021-01845-z
Source DB: PubMed Journal: Eur Child Adolesc Psychiatry ISSN: 1018-8827 Impact factor: 4.785
Randomized controlled trials of psychological interventions for tic disorders published since 2011, as well as a selection* of previous influential trials to enable comparison
| Study | Groups | Subjects | Efficacy | Follow-up | Comments |
|---|---|---|---|---|---|
| Verdellen et al. (2004) [ | HRT vs ERP | Age 7–55 | HRT: 24.1 (pre) to 19.7 (post) Within-group effect size: 1.06 ERP: 26.2 (pre) to 17.6 (post) Within-group effect size: 1.42 | HRT: 13.5 ERP: 14.0 | |
| Piacentini et al. (2010) [ | CBIT vs PST | Age 9–17 | CBIT: 24.7 (pre) to 17.1 (post) PST: 24.6 (pre) to 21.1 (post) Between-group effect size: 0.68 | CBIT: 20 out of 23 available initial treatment responders were still classified as treatment responders (according to the CGI-I) | |
| Himle et al. (2012) [ | F2F CBIT vs VC CBIT | Age 8–17 | F2F CBIT: 24.1 (pre) to 17.6 (post) VC CBIT: 23.4 (pre) to 15.6 (post) | F2F CBIT: 20.1 VC CBIT: 16.8 | |
| Wilhelm et al. (2012) [ | CBIT vs PST | Age 16–69 | CBIT: 24.0 (pre) to 17.8 (post) PST: 21.8 (pre) to 19.3 (post) Between-group effect size: 0.57 | CBIT: 12 out of 15 available initial treatment responders were still classified as treatment responders (according to the CGI-I) | |
| McGuire et al. (2015) [ | LWT vs Waitlist | Pediatric sample | LWT: 20.2 (pre) to 14.3 (post) Waitlist: 24.7 (pre) to 24.8 (post) LWT: 27.5 (pre) to 8.3 (post) Waitlist: 31.7 (pre) to 23.8 (post) Between-group effect size: 1.50 | 1FU was completed for 5 out of 10 initial treatment responders (according to the CGI-I). No change was found between the post and 1FU YGTSS Impairment scores, indicating maintenance of the treatment effects | |
| Ricketts et al. (2016) [ | VC CBIT vs Waitlist | Age 8–16 | VC CBIT: 25.8 (pre) to 18.5 (post) Waitlist: 22.0 (pre) to 20.3 (post) Between-group effect size: 0.15 (partial η2) | N/a | |
| Yates et al. (2016) [ | Group HRT vs Group PE | Age 9–13 | N/a Group HRT: 17.7 (pre) to 15.1 (post) Group PE: 16.3 (pre) to 15.9 (post) Between-group effect size: 0.55 | Group HRT: 12.2 Group PE: 13.8 | |
| Seragni et al. (2018) [ | HRT vs UC | Pediatric sample | N/a | Significant within-group effect for HRT and UC combined into one group. Scores n/a | |
| Rizzo et al. (2018) [ | BT vs. PE PT vs. PE BT vs. PT | Age 8–17 | BT: 19.8 (pre) to 11.4 (post) PT: 24.1 (pre) to 15.7 (post) PE: 22.0 (pre) to 21.7 (post) | BT: 12.4 PT: 14.7 PE: 20.7 | |
| Andrén et al. (2019) [ | Internet ERP vs. Internet HRT | Age 8–16 | Internet ERP: 23.8 (pre) to 18.3 (3FU) Within-group effect size: 1.12 Internet HRT: 23.5 (pre) to 20.2 (3FU) Within-group effect size: 0.50 | Internet ERP: 16.9 Internet HRT: 19.4 | |
| Nissen et al. (2019, 2021) [ | Individual HRT + ERP vs Group HRT + ERP | Age 9–17 | Individual HRT + ERP: 23.8 (pre) to 14.3 (post) Within-group effect size: 1.21 Group HRT + ERP: 23.4 (pre) to 15.9 (post) Within-group effect size: 1.38 | Individual HRT + ERP: 12.7 Group HRT + ERP: 12.8 | |
| Chen et al. (2020) [ | CBIT + UC vs. UC | Age 6–18 | CBIT: 19.3 (pre) to 10.4 (post) UC: 17.7 (pre) to 14.5 (post) Between-group effect size: 0.56 | CBIT: 6.6 | |
| McGuire et al. (2020) [ | HRT + DCS vs. HRT + placebo | Age 8–17 | N/a | N/a | |
| Rachamim et al. (2020) [ | Internet CBIT vs. Waitlist | Age 7–18 | Internet CBIT: 22.7 (pre) to 16.1 (post) Waitlist: 21.9 (pre) to 20.9 (post) Between-group effect size: 0.20 (partial η2) | Internet CBIT: 11.0 | |
| Singer et al. (2020) [ | DVD HRT vs. HRT | Age 7–13 | DVD HRT: 27.8 (pre) to 18.8 (post) HRT: 28.2 (pre) to 20.7 (post) | N/a | |
| Zimmerman-Brenner et al. (2021) [ | Group CBIT vs. Group PE | Age 8–15 | Group CBIT: 24.8 (pre) to 39.8 (post) Group PE: 22.0 (pre) to 37.1 (post) | Group CBIT: 18.4 Group PE: 21.8 |
*The previous trials were selected following expert consensus as especially important for the recommendations of the initial European clinical guidelines published in 2011
1–3−4–6−12FU 1–3-4–6-12 months post-treatment time-point follow-up; BT behavior therapy; CBIT comprehensive behavioral intervention for tics; CGI−I Clinical Global Impressions—Improvement scale; CTD chronic tic disorder; DCS d-cycloserine; ERP exposure and response prevention; F2F face-to-face; FU follow-up; HRT habit reversal training; LWT Living with tics; N/a not available; PE psychoeducation; post post-treatment time-point; pre pre-treatment/baseline time-point; PST psychoeducation and supportive psychotherapy; PT pharmacotherapy; TS Tourette syndrome; UC usual care; VC videoconference; YGTSS Yale Global Tic Severity Scale; YGTSS−MTSS Yale Global Tic Severity Scale—Motor Tic Severity Score; YGTSS−TTS Yale Global Tic Severity Scale—Total Tic Severity Score