Literature DB >> 25111654

The National ALS Registry: a recruitment tool for research.

Angela M Malek1, David E Stickler, Vinicius C Antao, D Kevin Horton.   

Abstract

INTRODUCTION: Subject recruitment is critical for understanding fatal diseases like ALS, however linking patients with researchers can be challenging. The U.S. population-based National ALS Registry allows recruitment of persons with ALS (PALS) for research opportunities.
METHODS: The Registry's Research Notification Mechanism was used to recruit PALS aged ≥21 years; participants completed a Web-based epidemiologic survey. PALS (n = 2,232) were sent an email describing the study, and 268 surveys were completed.
RESULTS: The mean age (± SD) of eligible participants was 57.7 ± 9.3 years for men and 61.5 ± 8.9 for women. Most were men (63%) and Caucasian (92%). Of 256 potentially eligible participants, 37.5% (n = 96) returned an authorization to disclose protected health information. ALS was confirmed for 94% (83/88) from physician responses.
CONCLUSIONS: This analysis demonstrates the National ALS Registry's usefulness in recruiting PALS for research. This recruitment source can potentially foster the discovery of better treatment options and therapies, and of prevention strategies.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  ALS; National ALS Registry; amyotrophic lateral sclerosis; recruitment; research

Mesh:

Year:  2014        PMID: 25111654      PMCID: PMC4206601          DOI: 10.1002/mus.24421

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  8 in total

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2.  The National Amyotrophic Lateral Sclerosis (ALS) Registry.

Authors:  Vinicius C Antao; D Kevin Horton
Journal:  J Environ Health       Date:  2012 Jul-Aug       Impact factor: 1.179

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Authors:  Anne-Marie Wills; Jane Hubbard; Eric A Macklin; Jonathan Glass; Rup Tandan; Ericka P Simpson; Benjamin Brooks; Deborah Gelinas; Hiroshi Mitsumoto; Tahseen Mozaffar; Gregory P Hanes; Shafeeq S Ladha; Terry Heiman-Patterson; Jonathan Katz; Jau-Shin Lou; Katy Mahoney; Daniela Grasso; Robert Lawson; Hong Yu; Merit Cudkowicz
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Authors:  Yanli Zhao; Merit E Cudkowicz; Jeremy M Shefner; Lisa Krivickas; William S David; Francine Vriesendorp; Alan Pestronk; James B Caress; Jonathan Katz; Ericka Simpson; Jeffrey Rosenfeld; Robert Pascuzzi; Jonathan Glass; Kourosh Rezania; Jerold S Harmatz; David Schoenfeld; David J Greenblatt
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7.  Dexpramipexole versus placebo for patients with amyotrophic lateral sclerosis (EMPOWER): a randomised, double-blind, phase 3 trial.

Authors:  Merit E Cudkowicz; Leonard H van den Berg; Jeremy M Shefner; Hiroshi Mitsumoto; Jesus S Mora; Albert Ludolph; Orla Hardiman; Michael E Bozik; Evan W Ingersoll; Donald Archibald; Adam L Meyers; Yingwen Dong; Wildon R Farwell; Douglas A Kerr
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Authors:  Angela M Malek; Aaron Barchowsky; Robert Bowser; Terry Heiman-Patterson; David Lacomis; Sandeep Rana; Ada Youk; David Stickler; Daniel T Lackland; Evelyn O Talbott
Journal:  Neurodegener Dis       Date:  2013-11-12       Impact factor: 2.977

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5.  Designing an Internationally Accessible Web-Based Questionnaire to Discover Risk Factors for Amyotrophic Lateral Sclerosis: A Case-Control Study.

Authors:  Jane Alana Parkin Kullmann; Susan Hayes; Min-Xia Wang; Roger Pamphlett
Journal:  JMIR Res Protoc       Date:  2015-08-03

6.  Patients with sporadic and familial amyotrophic lateral sclerosis found value in genetic testing.

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Journal:  Mol Genet Genomic Med       Date:  2017-12-20       Impact factor: 2.183

7.  Recruitment of Patients With Amyotrophic Lateral Sclerosis for Clinical Trials and Epidemiological Studies: Descriptive Study of the National ALS Registry's Research Notification Mechanism.

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  7 in total

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