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A Measurement Study of TIS-modNV and AccuGait Force Platform in People With MS

N

Nordlandssykehuset HF

Status

Not yet enrolling

Conditions

Multiple Sclerosis

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT05503628
HNF1608-21 (Other Grant/Funding Number)
Trunk & balance tests in MS

Details and patient eligibility

About

The current project will fill a knowledge gap in the follow-up of people with Multiple Sclerosis (MS) with mild and moderate disability levels, with the purpose to assess the adequacy of measurement tools for trunk control and balance, functions that are pre-requisites for optimal performance in everyday physical activities.

Full description

Trunk control and balance, necessary for daily activities, are frequently impaired in people with MS. Adequate measurement tools for clinical- and research purposes are thus warranted. In this study two measurement tools will be explored:

  1. The Trunk Impairment scale - modified Norwegian version (TIS-modNV), which has demonstrated high validity and reliability in individuals with stoke (Gjelsvik et al., 2012), however its properties has not yet been assessed in people with MS. Concurrent validity with a balance scale, the Mini-Balance Evaluation Systems Test (Mini-BESTest), will be assessed as well as its inter- and intra-rater reliability.
  2. The AMTI Accugait Optimized™ multi-axis force platform (AMTI, Inc., Newton, MA) will be examined as there is a lack of studies measuring its properties within the MS population. A validity assessment of this tool will be included in this measurement study.

This study is two-parted, each with a separate aim:

Aim part 1: To determine the validity and reliability of the TIS-modNV across mild and moderate disability levels in the MS population.

Aim part 2: To determine the concurrent validity of the AMTI AccuGait OptimizedTM force plate system compared to the Mini-BESTest across mild and moderate disability levels in the MS population.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • MS diagnosis (McDonalds criteria)
  • EDSS= 0-6.5
  • Ability to walk minimum 6 meters

Exclusion criteria

  • People will be excluded if not being able to follow test instructions

Trial contacts and locations

1

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Central trial contact

Stine Susanne Haakonsen Dahl, MSc; Ellen Christin Arntzen, PHD

Data sourced from clinicaltrials.gov

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