Actively Recruiting

Age: 18Years - 65Years
All Genders
Healthy Volunteers
ID07505355

Measurement Properties of the Walking Adaptability Ladder Test and Foot Tap Test in People With Multiple Sclerosis With Mild Disability

Led by Hasselt University · Updated on 2026-04-01

100

Participants Needed

4

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Walking and motor control difficulties are common in people with multiple sclerosis (pwMS), even in those with mild disability. Early changes in walking can signal disease progression, but current tests mainly measure time or distance and may miss subtle changes. This research focuses on better ways to assess walking adaptability, which involves adjusting walking patterns in response to challenges like fatigue and balance. The study aims to evaluate two tests, the Walking Adaptability Ladder Test (WALT) and the Foot Tap Test (FTT), in pwMS with mild disability to see how reliable and valid they are. The study will include 50 people with multiple sclerosis and 50 healthy controls matched by age and sex. Participants will complete the WALT, FTT, Balance Recovery Scale, and Gait-Specific Attention Profile twice, one week apart, to test reliability. Additional walking and motor function tests will be performed, including the Timed 25-Foot Walk and the 6-Minute Walk Test. Cognitive processing speed and patient-reported outcomes about walking limitations, fatigue, balance confidence, and fall concerns will also be collected. Data will be gathered in Spain, Italy, and Belgium, with retests performed in Spain. Participants will be assessed through various motor and walking tests, questionnaires, and wearable sensors to record movement. The study will analyze the consistency and accuracy of these tests and compare performance between pwMS and healthy controls. The main measurements are the WALT and FTT performed on two separate days. The research will help identify which tests best detect subtle walking impairments and how clinical test results relate to patients' self-reported experiences. The study participation spans the test days and follow-up for reliability testing.

CONDITIONS

Brief Title

Measurement Properties of the Walking Adaptability Ladder Test and Foot Tap Test in Multiple Sclerosis

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed diagnosis of definite multiple sclerosis
  • Relapse free for at least 30 days
  • Expanded Disability Status Scale (EDSS) score between 0 and 3.5
  • Age between 18 and 65 years
  • Both males and females are eligible
Not Eligible

You will not qualify if you...

  • Diagnosed with neurological diseases other than multiple sclerosis
  • Cognitive decline that prevents performing tests and questionnaires
  • Other neurological, orthopedic, or visual impairments affecting walking

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - 2 consecutive days

Participants complete walking and motor function tests, cognitive assessments, and patient-reported outcomes to evaluate walking adaptability and motor abilities.

2 visits (in-person) on consecutive days

Long-term Monitoring

Duration - Up to study completion date

Data from initial assessments are combined with other data to analyze test reliability, validity, and group comparisons.

No additional visits required

Trial Site Locations

Total: 4 locations

1

REVAL Rehabilitation Research Center

Diepenbeek, Belgium

Actively Recruiting

2

Laboratorio di Biomeccanica ed Ergonomia industriale Università degli Studi di Cagliari

Cagliari, Italy

Actively Recruiting

3

Hospital Universitario de Ponferrada El Bierzo

León, Ponferrada, Spain

Actively Recruiting

4

University of Leon

León, Ponferrada, Spain

Actively Recruiting

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Research Team

Z

Zuhal Abasiyanik, PhD

P

Peter Feys

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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