Reliability and Validity of Outcome Measures for Pain in Multiple Sclerosis

NCT ID: NCT05742152

Last Updated: 2024-07-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-04-01

Study Completion Date

2024-05-01

Brief Summary

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This project aims to provide values of test-retest reliability and insights from concurrent validity of outcome measures for pain in multiple sclerosis.

Detailed Description

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Pain is one of the most annoying symptoms in multiple sclerosis (MS). However, it is underestimated albeit its high prevalence rate with 63%. It negatively affects health related quality of life, activity of daily living, mental health, social functioning, employment, sleep and life enjoyment. In literature, the prevalence of pain varies in the MS literature from 29% to 86%. This wide-range prevalence is the result of methodological differences and non-uniformity of the studied populations which makes pain unclear and underdiagnosed in multiple sclerosis.It is hypothesized that the consistency, severity and interference of pain have varying relationships between other factors such as depression, anxiety, sleep or fatigue.

Evaluating pain was done with various outcome measures resulting in inconclusive results. However, very few of the pain outcome measures are validated for MS population. Thus, it cannot be advised yet whether they contain similar or complementary information. Finally, the interference of pain on activities and participation level of the International Classification of Functioning, Disability and Health (ICF) is poorly documented.

This project aims to put the foundations for future interventional research by providing values of test-retest reliability and insights from concurrent validity. As well, the perceived interference from pain on activities and participation level will be documented.

Conditions

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Pain

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Age 18 and above,
* Ambulatory pwMS with definite diagnosis based on McDonald criteria
* Expanded Disability Status Scale of 6.0 or below,
* Having pain in last month
* Able to understand and answer the questions in the questionnaires.

Exclusion Criteria

* Diagnosed with major musculoskeletal disorder and any neurological disorder other than MS,
* a relapse in the last month before enrolment,
* cognitive decline that renders the patient incapable of performing tests and questionnaires,
* patients with only headache
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hasselt University

OTHER

Sponsor Role lead

Responsible Party

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Peter Feys

Prof. dr.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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National MS center

Melsbroek, Brabant, Belgium

Site Status

Noorderhart

Overpelt, Limburg, Belgium

Site Status

AZ Sint-Jan

Bruges, , Belgium

Site Status

Pontificia universidad catolica de Chile

Santiago, , Chile

Site Status

Countries

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Belgium Chile

References

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Yilmazer C, D'haeseleer M, Soler B, Van Wijmeersch B, Solaro C, Ciampi E, Carcamo C, Van Asch P, Cambron M, Lamers I, Feys P. Assessing pain in multiple sclerosis: Test-retest reliability of patient-reported outcome measures and accuracy of screening tools. Mult Scler. 2025 Apr;31(4):474-488. doi: 10.1177/13524585241310139. Epub 2025 Jan 16.

Reference Type DERIVED
PMID: 39819131 (View on PubMed)

Other Identifiers

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B1152022000014

Identifier Type: -

Identifier Source: org_study_id

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