Validation of the freezing of gait questionnaire in patients with Parkinson's disease
Identifieur interne : 000231 ( France/Analysis ); précédent : 000230; suivant : 000232Validation of the freezing of gait questionnaire in patients with Parkinson's disease
Auteurs : Nir Giladi [Israël] ; Joseph Tal [Israël] ; Tali Azulay [Israël] ; Olivier Rascol [France] ; David J. Brooks [Royaume-Uni] ; Eldad Melamed [Israël] ; Wolfgang Oertel [Allemagne] ; Werner Poewe [Autriche] ; Fabrizio Stocchi [Italie] ; Eduardo Tolosa [Espagne]Source :
- Movement Disorders [ 0885-3185 ] ; 2009-04-15.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Congélation, Homme.
English descriptors
- KwdEn :
- Aged, Analysis of Variance, Antiparkinson Agents (adverse effects), Antiparkinson Agents (therapeutic use), Catechols (therapeutic use), Double-Blind Method, Female, Freezing, Freezing Reaction, Cataleptic (drug effects), Freezing Reaction, Cataleptic (physiology), Gait Disorders, Neurologic (chemically induced), Gait Disorders, Neurologic (diagnosis), Gait Disorders, Neurologic (drug therapy), Gait Disorders, Neurologic (physiopathology), Human, Humans, Indans (therapeutic use), Levodopa (adverse effects), Male, Middle Aged, Nervous system diseases, Neuroprotective Agents (therapeutic use), Nitriles (therapeutic use), Parkinson Disease (drug therapy), Parkinson disease, Parkinson's disease, Principal Component Analysis, Psychiatric Status Rating Scales, Questionnaire, Questionnaires, Rasagiline, Reproducibility of Results, Severity of Illness Index, Statistics as Topic, Validation, freezing of gait, rasagiline, validation.
- MESH :
- chemical , adverse effects : Antiparkinson Agents, Levodopa.
- chemical , therapeutic use : Antiparkinson Agents, Catechols, Indans, Neuroprotective Agents, Nitriles.
- chemically induced : Gait Disorders, Neurologic.
- diagnosis : Gait Disorders, Neurologic.
- drug effects : Freezing Reaction, Cataleptic.
- drug therapy : Gait Disorders, Neurologic, Parkinson Disease.
- physiology : Freezing Reaction, Cataleptic.
- physiopathology : Gait Disorders, Neurologic.
- Aged, Analysis of Variance, Double-Blind Method, Female, Humans, Male, Middle Aged, Principal Component Analysis, Psychiatric Status Rating Scales, Questionnaires, Reproducibility of Results, Severity of Illness Index, Statistics as Topic.
Abstract
To revalidate the Freezing of Gait Questionnaire (FOG‐Q), patients with Parkinson's disease (PD) were randomly assigned to receive rasagiline (1 mg/day) (n = 150), entacapone (200 mg with each dose of levodopa) (n = 150), or placebo (n = 154). Patients were assessed at baseline and after 10 weeks using the FOG‐Q, Unified Parkinson's Disease Rating Scale (UPDRS), Beck Depression Inventory (BDI), and Parkinson's Disease Questionnaire (PDQ‐39). FOG‐Q dimensionality, test–retest reliability, and internal reliability were examined. Convergent and divergent validities were assessed by correlating FOG‐Q with UPDRS, BDI, and PDQ‐39. Comparisons between FOG‐Q item 3 and UPDRS item 14 were also made. Principal component analysis indicated that FOG‐Q measures a single dimension. Test–retest reliability and internal reliability of FOG‐Q score was high. FOG‐Q was best correlated to items of the UPDRS relating to walking, general motor issues, and mobility. Correlations between baseline and endpoint suggested that FOG‐Q item 3 is at least as reliable as UPDRS item 14. At baseline, 85.9% of patients were identified as “Freezers” using FOG‐Q item 3 (≥1) and 44.1% using UPDRS item 14 (≥1) (P < 0.001). FOG‐Q was a reliable tool for the assessment of treatment intervention. FOG‐Q item 3 was effective as a screening question for the presence of FOG. © 2007 Movement Disorder Society
Url:
DOI: 10.1002/mds.21745
Affiliations:
- Allemagne, Autriche, Espagne, France, Israël, Italie, Royaume-Uni
- Angleterre, Catalogne, District de Giessen, Grand Londres, Hesse (Land), Latium, Midi-Pyrénées, Tyrol (Land)
- Barcelone, Innsbruck, Londres, Marbourg, Rome, Toulouse
- Université Toulouse III - Paul Sabatier, Université de Toulouse, Université de médecine d'Innsbruck
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<term>Antiparkinson Agents (therapeutic use)</term>
<term>Catechols (therapeutic use)</term>
<term>Double-Blind Method</term>
<term>Female</term>
<term>Freezing</term>
<term>Freezing Reaction, Cataleptic (drug effects)</term>
<term>Freezing Reaction, Cataleptic (physiology)</term>
<term>Gait Disorders, Neurologic (chemically induced)</term>
<term>Gait Disorders, Neurologic (diagnosis)</term>
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<term>Gait Disorders, Neurologic (physiopathology)</term>
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<term>Principal Component Analysis</term>
<term>Psychiatric Status Rating Scales</term>
<term>Questionnaire</term>
<term>Questionnaires</term>
<term>Rasagiline</term>
<term>Reproducibility of Results</term>
<term>Severity of Illness Index</term>
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<term>freezing of gait</term>
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<front><div type="abstract" xml:lang="en">To revalidate the Freezing of Gait Questionnaire (FOG‐Q), patients with Parkinson's disease (PD) were randomly assigned to receive rasagiline (1 mg/day) (n = 150), entacapone (200 mg with each dose of levodopa) (n = 150), or placebo (n = 154). Patients were assessed at baseline and after 10 weeks using the FOG‐Q, Unified Parkinson's Disease Rating Scale (UPDRS), Beck Depression Inventory (BDI), and Parkinson's Disease Questionnaire (PDQ‐39). FOG‐Q dimensionality, test–retest reliability, and internal reliability were examined. Convergent and divergent validities were assessed by correlating FOG‐Q with UPDRS, BDI, and PDQ‐39. Comparisons between FOG‐Q item 3 and UPDRS item 14 were also made. Principal component analysis indicated that FOG‐Q measures a single dimension. Test–retest reliability and internal reliability of FOG‐Q score was high. FOG‐Q was best correlated to items of the UPDRS relating to walking, general motor issues, and mobility. Correlations between baseline and endpoint suggested that FOG‐Q item 3 is at least as reliable as UPDRS item 14. At baseline, 85.9% of patients were identified as “Freezers” using FOG‐Q item 3 (≥1) and 44.1% using UPDRS item 14 (≥1) (P < 0.001). FOG‐Q was a reliable tool for the assessment of treatment intervention. FOG‐Q item 3 was effective as a screening question for the presence of FOG. © 2007 Movement Disorder Society</div>
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