Movement Disorders (revue)

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A Randomized, Double-Blind Trial of Transcranial Electrostimulation in Early Parkinson's Disease

Identifieur interne : 000515 ( PascalFrancis/Corpus ); précédent : 000514; suivant : 000516

A Randomized, Double-Blind Trial of Transcranial Electrostimulation in Early Parkinson's Disease

Auteurs : Holly A. Shill ; Sanja Obradov ; Yakov Katsnelson ; Ray Pizinger

Source :

RBID : Pascal:11-0353391

Descripteurs français

English descriptors

Abstract

We studied the effects of noninvasive transcranial electrical stimulation on the motor and psychological symptoms of early Parkinson's disease. Twenty-three subjects were treated with 10 days of placebo versus active treatment and then followed for 14 weeks. Baseline off medication Unified Parkinson's Disease Rating Scale parts I-III was 29.4 ± 10.0. The primary end point, Unified Parkinson's Disease Rating Scale in week 2 following treatment, reduced by 5.3 ± 9.7 for those in active treatment and 7.7 ± 4.8 for those receiving placebo (not significant). Similarly, no significant differences were seen in the Hamilton Anxiety Scale, Geriatric Depression Scale, and Epworth Sleepiness Scale over the duration of the study. The treatment was well tolerated without device-related adverse events. Despite the negative study, nonpharmacological approaches should continue to be pursued in Parkinson's disease, as they are generally well received by patients.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A03   1    @0 Mov. disord.
A05       @2 26
A06       @2 8
A08 01  1  ENG  @1 A Randomized, Double-Blind Trial of Transcranial Electrostimulation in Early Parkinson's Disease
A11 01  1    @1 SHILL (Holly A.)
A11 02  1    @1 OBRADOV (Sanja)
A11 03  1    @1 KATSNELSON (Yakov)
A11 04  1    @1 PIZINGER (Ray)
A14 01      @1 Banner Sun Health Research Institute @2 Sun City, Arizona @3 USA @Z 1 aut. @Z 2 aut.
A14 02      @1 Kalaco Scientific, Inc @2 Scottsdale, Arizona @3 USA @Z 3 aut. @Z 4 aut.
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A43 01      @1 INIST @2 20953 @5 354000508552620150
A44       @0 0000 @1 © 2011 INIST-CNRS. All rights reserved.
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A47 01  1    @0 11-0353391
A60       @1 P
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C01 01    ENG  @0 We studied the effects of noninvasive transcranial electrical stimulation on the motor and psychological symptoms of early Parkinson's disease. Twenty-three subjects were treated with 10 days of placebo versus active treatment and then followed for 14 weeks. Baseline off medication Unified Parkinson's Disease Rating Scale parts I-III was 29.4 ± 10.0. The primary end point, Unified Parkinson's Disease Rating Scale in week 2 following treatment, reduced by 5.3 ± 9.7 for those in active treatment and 7.7 ± 4.8 for those receiving placebo (not significant). Similarly, no significant differences were seen in the Hamilton Anxiety Scale, Geriatric Depression Scale, and Epworth Sleepiness Scale over the duration of the study. The treatment was well tolerated without device-related adverse events. Despite the negative study, nonpharmacological approaches should continue to be pursued in Parkinson's disease, as they are generally well received by patients.
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C03 03  X  ENG  @0 Depression @5 03
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Format Inist (serveur)

NO : PASCAL 11-0353391 INIST
ET : A Randomized, Double-Blind Trial of Transcranial Electrostimulation in Early Parkinson's Disease
AU : SHILL (Holly A.); OBRADOV (Sanja); KATSNELSON (Yakov); PIZINGER (Ray)
AF : Banner Sun Health Research Institute/Sun City, Arizona/Etats-Unis (1 aut., 2 aut.); Kalaco Scientific, Inc/Scottsdale, Arizona/Etats-Unis (3 aut., 4 aut.)
DT : Publication en série; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2011; Vol. 26; No. 8; Pp. 1477-1480; Bibl. 19 ref.
LA : Anglais
EA : We studied the effects of noninvasive transcranial electrical stimulation on the motor and psychological symptoms of early Parkinson's disease. Twenty-three subjects were treated with 10 days of placebo versus active treatment and then followed for 14 weeks. Baseline off medication Unified Parkinson's Disease Rating Scale parts I-III was 29.4 ± 10.0. The primary end point, Unified Parkinson's Disease Rating Scale in week 2 following treatment, reduced by 5.3 ± 9.7 for those in active treatment and 7.7 ± 4.8 for those receiving placebo (not significant). Similarly, no significant differences were seen in the Hamilton Anxiety Scale, Geriatric Depression Scale, and Epworth Sleepiness Scale over the duration of the study. The treatment was well tolerated without device-related adverse events. Despite the negative study, nonpharmacological approaches should continue to be pursued in Parkinson's disease, as they are generally well received by patients.
CC : 002B17; 002B17G
FD : Maladie de Parkinson; Angoisse anxiété; Etat dépressif; Pathologie du système nerveux
FG : Pathologie de l'encéphale; Syndrome extrapyramidal; Maladie dégénérative; Pathologie du système nerveux central; Affect affectivité; Trouble de l'humeur
ED : Parkinson disease; Anxiety; Depression; Nervous system diseases
EG : Cerebral disorder; Extrapyramidal syndrome; Degenerative disease; Central nervous system disease; Affect affectivity; Mood disorder
SD : Parkinson enfermedad; Angustia ansiedad; Estado depresivo; Sistema nervioso patología
LO : INIST-20953.354000508552620150
ID : 11-0353391

Links to Exploration step

Pascal:11-0353391

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<SD>Parkinson enfermedad; Angustia ansiedad; Estado depresivo; Sistema nervioso patología</SD>
<LO>INIST-20953.354000508552620150</LO>
<ID>11-0353391</ID>
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