Skip to main content
OpenTrials
Completed

NCT Number: NCT02227524

Trekking Poles to Aid Multiple Sclerosis Gait Impairment

In this study, the investigators will examine a sample of persons with multiple sclerosis (MS) to determine whether their walking function and ability is different depending on which walking assistive device is used.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–64 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Rowan University School of Osteopathic Medicine

Stratford, New Jersey, 08084, United States

About this study

In this study, the investigators will examine a sample of persons with multiple sclerosis (MS) to determine whether their walking function and ability is different depending on which walking assistive device is used. In addition, the investigators will examine the psychosocial impact and amount of fatigue induced by each assistive device. Data collection will consist of a series of assessments via survey and physical performance. The analyses will consist of appropriate comparisons of means to determine if the use of different assistive devices alters any of the outcomes.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Be 18-64 years old with a confirmed diagnosis of MS
  • Have perceived walking difficulty
  • Have an EDSS score of < 6, calculated by the physician
  • Ability to understand study procedures and to comply with them for the entire length of the study

Exclusion criteria

  • Have had a MS exacerbation in the prior 8 weeks
  • Have other serious medical conditions that would impair their ability to participate in gait performance testing (i.e. severe rheumatoid arthritis or osteoarthritis)
  • If the physician deems a participant unsafe to go home with devices
  • Cannot communicate in English
  • Possess greater than a mild decrease in mentation (i.e. a score of >2 on the Mental Functions item of the FSS)
  • Inability or unwillingness of individual to give written informed consent

Treatment and study plan

No device

Other

Compare walking function and ability in a sample of persons with MS under four different assistive device conditions: no device, single-point cane (SPC), four-point cane (FPC) and trekking pole (TP).

Single-point cane (SPC)

Device

Compare walking function and ability in a sample of persons with MS under four different assistive device conditions: no device, single-point cane (SPC), four-point cane (FPC) and trekking pole (TP).

Four-point cane (FPC)

Device

Compare walking function and ability in a sample of persons with MS under four different assistive device conditions: no device, single-point cane (SPC), four-point cane (FPC) and trekking pole (TP).

Trekking pole (TP).

Device

Compare walking function and ability in a sample of persons with MS under four different assistive device conditions: no device, single-point cane (SPC), four-point cane (FPC) and trekking pole (TP).

Primary outcomes

  1. Composite measures of walking

    Time frame: 1 year

    Temporal and spatial parameters of gait/walking (measured with the GAITRite portable walkway system)

Sponsors and collaborators

Lead sponsor

Rowan University

Other

Registry information

Acronym: TRAMS

Important dates

Study start
2014
Primary completion
2019
Study completion
2019
First posted
Aug 28, 2014
Registry last updated
Apr 11, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.