Literature DB >> 15026500

The MS Symptom and Impact Diary (MSSID): psychometric evaluation of a new instrument to measure the day to day impact of multiple sclerosis.

J Greenhalgh1, H Ford, A F Long, K Hurst.   

Abstract

OBJECTIVES: This study aimed to develop further a diary originally devised to measure the impact of multiple sclerosis (MS) as part of a cost utility study of beta interferon, and to evaluate its reliability, validity, and responsiveness in an outpatient sample of people with MS.
METHODS: The original diary was further developed using qualitative and quantitative methods to ensure that it addressed the views of people with MS. The psychometric properties of the MS Symptom and Impact Diary (MSSID) were evaluated in a sample of 77 people who completed the MSSID daily for 12 weeks. Internal and test-retest reliability, discriminant and convergent validity, and responsiveness were assessed using traditional psychometric methods.
RESULTS: The MSSID formed three, internally consistent scales that measured mobility, fatigue, and the overall impact of MS. The test-retest reliability of the mobility scale was adequate for individual comparisons (ICC>0.90) and the fatigue and overall impact scales were adequate for group comparisons (ICC>0.70). The MSSID was able to distinguish between clinical groups depending on clinical course, indoor ambulation status, and relapse status. It demonstrated associations with other single point instruments in the expected direction. Compared with single point instruments, its responsiveness was similar or better, especially in detecting short term improvements in functioning.
CONCLUSIONS: The MSSID may provide a useful complement to currently available instruments to measure the outcomes of MS within clinical trials. Further research is needed to explore its feasibility in the context of a randomised controlled trial and its utility for clinicians.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15026500      PMCID: PMC1739024          DOI: 10.1136/jnnp.2003.020529

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  33 in total

Review 1.  Assessing relapses in treatment trials of relapsing and remitting multiple sclerosis: can we do better?

Authors:  C Liu; L D Blumhardt
Journal:  Mult Scler       Date:  1999-02       Impact factor: 6.312

2.  Quality of life in multiple sclerosis.

Authors:  P M Rothwell
Journal:  J Neurol Neurosurg Psychiatry       Date:  1998-10       Impact factor: 10.154

3.  Reviewing and selecting outcome measures for use in routine practice.

Authors:  J Greenhalgh; A F Long; A J Brettle; M J Grant
Journal:  J Eval Clin Pract       Date:  1998-11       Impact factor: 2.431

4.  Outcome research in neurology: incorporating health-related quality of life.

Authors:  O Devinsky
Journal:  Ann Neurol       Date:  1995-02       Impact factor: 10.422

5.  Sense making in multiple sclerosis: the information needs of people during an acute exacerbation.

Authors:  L M Baker
Journal:  Qual Health Res       Date:  1998-01

6.  A systematic overview of the use of diary cards, quality-of-life questionnaires, and psychometric tests in treatment trials of Helicobacter pylori-positive and -negative non-ulcer dyspepsia.

Authors:  G S Sandha; R H Hunt; S J Veldhuyzen van Zanten
Journal:  Scand J Gastroenterol       Date:  1999-03       Impact factor: 2.423

7.  A health-related quality of life measure for multiple sclerosis.

Authors:  B G Vickrey; R D Hays; R Harooni; L W Myers; G W Ellison
Journal:  Qual Life Res       Date:  1995-06       Impact factor: 4.147

8.  The journey to multiple sclerosis: a qualitative study.

Authors:  W Koopman; A Schweitzer
Journal:  J Neurosci Nurs       Date:  1999-02       Impact factor: 1.230

9.  The lived experience of relapsing multiple sclerosis: a phenomenological study.

Authors:  C M Miller
Journal:  J Neurosci Nurs       Date:  1997-10       Impact factor: 1.230

10.  Doctors and patients don't agree: cross sectional study of patients' and doctors' perceptions and assessments of disability in multiple sclerosis.

Authors:  P M Rothwell; Z McDowell; C K Wong; P J Dorman
Journal:  BMJ       Date:  1997-05-31
View more
  10 in total

1.  Health-related quality of life in relapsing remitting multiple sclerosis patients during treatment with glatiramer acetate: a prospective, observational, international, multi-centre study.

Authors:  Peter J Jongen; Dirk Lehnick; Evert Sanders; Pierette Seeldrayers; Sten Fredrikson; Magnus Andersson; Joachim Speck
Journal:  Health Qual Life Outcomes       Date:  2010-11-15       Impact factor: 3.186

2.  Variability of current symptoms in women with pelvic organ prolapse.

Authors:  Vivian W Sung; Melissa A Clark; Eric R Sokol; Charles R Rardin; Deborah L Myers
Journal:  Int Urogynecol J Pelvic Floor Dysfunct       Date:  2006-11-18

3.  An assessment of the feasibility and utility of the MS symptom and impact diary (MSSID).

Authors:  Joanne Greenhalgh
Journal:  Qual Life Res       Date:  2005-06       Impact factor: 4.147

4.  Electronic Health Diary Campaigns to Complement Longitudinal Assessments in Persons With Multiple Sclerosis: Nested Observational Study.

Authors:  Chloé Sieber; Deborah Chiavi; Christina Haag; Marco Kaufmann; Andrea B Horn; Holger Dressel; Chiara Zecca; Pasquale Calabrese; Caroline Pot; Christian Philipp Kamm; Viktor von Wyl
Journal:  JMIR Mhealth Uhealth       Date:  2022-10-05       Impact factor: 4.947

5.  Listening to patients: using verbal data in the validation of the Aberdeen Measures of Impairment, Activity Limitation and Participation Restriction (Ab-IAP).

Authors:  Jeremy Horwood; Beth Pollard; Salma Ayis; Teresa McIlvenna; Marie Johnston
Journal:  BMC Musculoskelet Disord       Date:  2010-08-12       Impact factor: 2.362

6.  Joint Healthcare Professional and Patient Development of Communication Tools to Improve the Standard of MS Care.

Authors:  Celia Oreja-Guevara; Stanca Potra; Birgit Bauer; Diego Centonze; Maria-Paz Giambastiani; Gavin Giovannoni; Jürg Kesselring; Dawn Langdon; Sarah A Morrow; Jocelyne Nouvet-Gire; Maija Pontaga; Peter Rieckmann; Sven Schippling; Nektaria Alexandri; Jane Shanahan; Heidi Thompson; Pieter Van Galen; Patrick Vermersch; David Yeandle
Journal:  Adv Ther       Date:  2019-09-05       Impact factor: 3.845

7.  Potentials and barriers of using digital tools for collecting daily measurements in multiple sclerosis research.

Authors:  Westergaard Katrine; Signe Baattrup Ritzel; Krogh Caroline; Lynning Marie; Bergien Sofie Olsgaard; Skovgaard Lasse
Journal:  Digit Health       Date:  2021-11-26

8.  Cost-effectiveness of multiple sclerosis disease-modifying therapies: a systematic review of the literature.

Authors:  David Yamamoto; Jonathan D Campbell
Journal:  Autoimmune Dis       Date:  2012-12-06

9.  A prospective web-based patient-centred interactive study of long-term disabilities, disabilities perception and health-related quality of life in patients with multiple sclerosis in The Netherlands: the Dutch Multiple Sclerosis Study protocol.

Authors:  Peter Joseph Jongen; Marco Heerings; Wim A Lemmens; Rogier Donders; Anneke van der Zande; Esther van Noort; Anton Kool
Journal:  BMC Neurol       Date:  2015-08-04       Impact factor: 2.474

10.  Responsiveness of the Multiple Sclerosis International Quality of Life questionnaire to disability change: a longitudinal study.

Authors:  Karine Baumstarck; Helmut Butzkueven; Oscar Fernández; Peter Flachenecker; Sergio Stecchi; Egemen Idiman; Jean Pelletier; Mohamed Boucekine; Pascal Auquier
Journal:  Health Qual Life Outcomes       Date:  2013-07-29       Impact factor: 3.186

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.