TY - JOUR
T1 - Habit reversal training in children and adolescents with chronic tic disorders
T2 - An Italian randomized, single-blind pilot study
AU - Seragni, Giorgio
AU - Chiappedi, Matteo
AU - Bettinardi, Barbara
AU - Zibordi, Federica
AU - Colombo, Timna
AU - Reina, Caterina
AU - Angelini, Lucia
PY - 2018/2/1
Y1 - 2018/2/1
N2 - BACKGROUND: The aim of the present study was to test the possibility to apply habit reversal training (HRTRT) in Italy and to evaluate the effectiveness of HRTRT in reducing tic severity compared with the "usual care" (UC) in Italian children and adolescents with Tourette Syndrome. MET HODS: We performed a single blind, randomized, pilot study comparing HRTRT (active treatment) and UC (usual treatment). Out of 69 patients seen during the study period, we were able to enroll 21 patients (11 randomized to HRTRT e 10 to UC). Assessment included in-depth neurological and psychiatric examination, K-SAD S-PL, YGTSS, KID SCREE N, GTS-QOL, CGI and C-GAS. All these evaluations but the K-SAD S-PL were used for baseline assessment but also one week after the end of treatment (T1) and then 3, 6 and 9 months later (respectively T2, T3, and T4). RESULTS: The sample was largely composed of patients of relevant clinical severity (CGI≥3: 85%). OCD and ADHD were the most frequent comorbidities (30% each). Only minor differences in terms of treatment effectiveness were found, although the HRTRT group turned out to include patients with more tics and a more compromised general functioning despite randomization. C ONCLUSIONS: We had a high number of patients who refused to be randomized (23 out of 69) and a high number of drop outs (27% in the HRT group, 50% in the UC group). There was an improvement in terms of reduced tics and improved global functioning in both groups, without significant changes in terms of Quality of Life.
AB - BACKGROUND: The aim of the present study was to test the possibility to apply habit reversal training (HRTRT) in Italy and to evaluate the effectiveness of HRTRT in reducing tic severity compared with the "usual care" (UC) in Italian children and adolescents with Tourette Syndrome. MET HODS: We performed a single blind, randomized, pilot study comparing HRTRT (active treatment) and UC (usual treatment). Out of 69 patients seen during the study period, we were able to enroll 21 patients (11 randomized to HRTRT e 10 to UC). Assessment included in-depth neurological and psychiatric examination, K-SAD S-PL, YGTSS, KID SCREE N, GTS-QOL, CGI and C-GAS. All these evaluations but the K-SAD S-PL were used for baseline assessment but also one week after the end of treatment (T1) and then 3, 6 and 9 months later (respectively T2, T3, and T4). RESULTS: The sample was largely composed of patients of relevant clinical severity (CGI≥3: 85%). OCD and ADHD were the most frequent comorbidities (30% each). Only minor differences in terms of treatment effectiveness were found, although the HRTRT group turned out to include patients with more tics and a more compromised general functioning despite randomization. C ONCLUSIONS: We had a high number of patients who refused to be randomized (23 out of 69) and a high number of drop outs (27% in the HRT group, 50% in the UC group). There was an improvement in terms of reduced tics and improved global functioning in both groups, without significant changes in terms of Quality of Life.
KW - Habits
KW - Tic disorders
KW - Tourette Syndrome
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U2 - 10.23736/S0026-4946.16.04344-9
DO - 10.23736/S0026-4946.16.04344-9
M3 - Article
AN - SCOPUS:85041011484
SN - 0026-4946
VL - 70
SP - 5
EP - 11
JO - Minerva Pediatrica
JF - Minerva Pediatrica
IS - 1
ER -