Evidence map›Paper›PMID 26715841›Full record

ArticlePatient preference and adherence2015

The interactive web-based program MSmonitor for self-management and multidisciplinary care in multiple sclerosis: concept, content, and pilot results.

Peter Joseph Jongen, Ludovicus G Sinnige, Björn M van Geel, Freek Verheul, Wim I Verhagen, Ruud A van der Kruijk, Reinoud Haverkamp, Hans M Schrijver, J Coby Baart, Leo H Visser and 8 more

Open access · goldAbstract read
In one paragraph

Article in Patient preference and adherence, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Trial
  2. Article
  3. Medication self-management toolkits for adults with multiple sclerosis: A scoping review.Exploratory research in clinical and social pharmacy · 2023
    Article
  4. Article
  5. Observational
  6. Article
  7. Review
  8. Review
  9. 'It struck at the heart of who I thought I was': A meta-synthesis of the qualitative literature examining the experiences of people with multiple sclerosis.Health expectations : an international journal of public participation in health care and health policy · 2020
    Review
  10. Patient and clinician perspectives on a patient-facing dashboard that visualizes patient reported outcomes in rheumatoid arthritis.Health expectations : an international journal of public participation in health care and health policy · 2020
    Article
  11. Article
  12. Article
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  14. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 13 institutions in 2 countries.

Peter Joseph JongenDepartment of Community and Occupational Medicine, University Medical Center Groningen, University Groningen, Groningen, the Netherlands ; MS4 Research Institute, Nijmegen, the Netherlands.
Ludovicus G SinnigeMultiple Sclerosis Centre Leeuwarden, Medical Centre Leeuwarden, Leeuwarden, the Netherlands.
Björn M van GeelDepartment of Neurology, Medical Centre Alkmaar, Alkmaar, the Netherlands.
Freek VerheulDepartment of Neurology, Groene Hart Hospital, Gouda, the Netherlands.
Wim I VerhagenDepartment of Neurology, Canisius Wilhelmina Hospital, Nijmegen, the Netherlands.
Ruud A van der KruijkDepartment of Neurology, Slingeland Hospital, Doetinchem, the Netherlands.
Reinoud HaverkampDepartment of Neurology, Zuwe Hofpoort Hospital, Woerden, the Netherlands.
Hans M SchrijverMultiple Sclerosis Centre, Westfries Gasthuis, Hoorn, the Netherlands.
J Coby BaartDepartment of Neurology, Ziekenhuisgroep Twente, Almelo-Hengelo, the Netherlands.
Leo H VisserMultiple Sclerosis Centre Midden Brabant, St Elisabeth Hospital, Tilburg, the Netherlands.
Edo P ArnoldusMultiple Sclerosis Centre Midden Brabant, Tweesteden Hospital, Tilburg, the Netherlands.
H Jacobus GilhuisDepartment of Neurology, Reinier de Graaf Gasthuis, Delft, the Netherlands.
Paul PopDepartment of Neurology, Viecuri Medical Centre, Venlo-Venray, the Netherlands.
Monique BooyMultiple Sclerosis Centre, Amphia Hospital, Breda, the Netherlands.
Wim LemmensDepartment for Health Evidence, Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands.
Rogier DondersDepartment for Health Evidence, Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands.
Anton KoolCuravista bv, Geertruidenberg, the Netherlands.
Esther van NoortCuravista bv, Geertruidenberg, the Netherlands.
Canisius-Wilhelmina Ziekenhuis · NLAmphia Ziekenhuis · NLElisabeth-TweeSteden Ziekenhuis · NLGroene Hart Ziekenhuis · NLMedisch Centrum Leeuwarden · NLRadboud University Medical Center · NLRadboud University Nijmegen · NLReinier de Graaf Hospital · NLSlingeland Ziekenhuis · NLSt. Elisabeth Hospital · CWUniversity Medical Center Groningen · NLVieCuri Medisch Centrum · NLZiekenhuis Groep Twente · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is a growing need to offer persons with multiple sclerosis (PwMS) possibilities for self-management and to integrate multidisciplinary health data. In 2009-2014 we developed a patient-reported outcome based, interactive, web-based program (MSmonitor) for (self-)monitoring, self-management and integrated, multidisciplinary care in MS.

methodsThe notions underlying the MSmonitor concept and the program's elements are described. We analyze MSmonitor's role in the self-management of fatigue by retrospective comparison of fatigue and health-related quality of life (HRQoL) before and after usage of specific elements of MSmonitor, and by a correlative analysis between frequency of usage and fatigue change.

resultsAfter a step-wise development the program comprises six validated questionnaires: Multiple Sclerosis Impact Profile, Modified Fatigue Impact Scale-5 items (MFIS-5), Hospital Anxiety and Depression Scale, Multiple Sclerosis Quality of Life-54 items, and the 8-item Leeds Multiple Sclerosis Quality of Life (LMSQoL) questionnaires; two inventories: Medication and Adherence Inventory, Miction Inventory; two diaries: Activities Diary, Miction Diary; and two functionalities: e-consult and personal e-logbook. The program is now used in 17 hospitals by 581 PwMS and their neurologists, MS nurses, physical therapists, rehabilitative doctors, continence nurses, and family doctors. Those PwMS (N=105) who used the LMSQoL and MFIS-5 questionnaires at least twice in a period of up to 6 months, showed improved HRQoL (P<0.026). In the subgroup (N=56) who had also used the Activities Diary twice or more, the frequency of diary usage correlated modestly with the degree of fatigue improvement (r=0.292; P=0.028).

conclusionMSmonitor is an interactive web-based program for self-management and integrated care in PwMS. Pilot data suggest that the repeated use of the short MFIS-5 and LMSQoL questionnaires is associated with an increase in HRQoL, and that a repeated use of the Activities Diary might contribute to the self-management of fatigue.

Indexed as

caremultidisciplinarymultiple sclerosispatient-reported outcomeself-managementweb-based

Identifiers

PMID26715841
PMCPMC4685885
OpenAlexW2208163614

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LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.