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Evaluating functional disability in clinical trials of lisdexamfetamine dimesylate in binge eating disorder using the Sheehan Disability Scale.
Yee, Karen S; Pokrzywinski, Robin; Hareendran, Asha; Shaffer, Shannon; Sheehan, David V.
Afiliação
  • Yee KS; Shire, a Member of the Takeda Group of Companies, Cambridge, Massachusetts, USA.
  • Pokrzywinski R; Patient-Centered Research, Evidera, Bethesda, Maryland, USA.
  • Hareendran A; Patient-Centered Research, Evidera, London, UK.
  • Shaffer S; Patient-Centered Research, Evidera, Bethesda, Maryland, USA.
  • Sheehan DV; University of South Florida College of Medicine, Tampa, Florida, USA.
Int J Methods Psychiatr Res ; 30(1): e1849, 2021 03.
Article em En | MEDLINE | ID: mdl-32841462
ABSTRACT

OBJECTIVES:

This study examined Sheehan Disability Scale (SDS) performance in binge eating disorder (BED) and explored relationships between SDS and BED outcomes using data from three placebo-controlled lisdexamfetamine (LDX) studies (two short-term, dose-optimized studies and one double-blind, randomized-withdrawal study) in adults with Diagnostic and Statistical Manual of Mental Disorders, fourth edition, text revision (DSM-IV-TR)-defined BED.

METHODS:

Analyses evaluated the psychometric properties of the SDS.

RESULTS:

Confirmatory factor analysis supported a unidimensional total score in the short-term studies, with internal consistency (Cronbach's α) being 0.878. Total score exhibited good construct validity, with moderate and statistically significant correlations observed with Yale-Brown Obsessive Compulsive Scale modified for binge eating, Binge Eating Scale (BES), and EuroQol Group 5-Dimension 5-Level health status index scores. Known-groups validity analysis for the short-term studies demonstrated a significantly lower total score at end of study in participants considered "not ill" versus "ill" based on Clinical Global Impressions-Severity scores. SDS total score changes in the short-term studies were greater in responders than nonresponders based on binge eating abstinence or BES score. In the randomized-withdrawal study, SDS scores increased relative to baseline to a greater extent in participants randomized to placebo than LDX.

CONCLUSIONS:

These analyses support the reliability, validity, and responsiveness to change of the SDS in individuals with BED.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno da Compulsão Alimentar / Dimesilato de Lisdexanfetamina Tipo de estudo: Clinical_trials / Guideline Limite: Adult / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtorno da Compulsão Alimentar / Dimesilato de Lisdexanfetamina Tipo de estudo: Clinical_trials / Guideline Limite: Adult / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article