Trekking Poles to Aid Multiple Sclerosis Gait Impairment

Rowan University29 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

OTHER

Masking

NONE

Enrollment

Conditions

Multiple Sclerosis

Interventions

No deviceOTHER

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).

Eligibility

Sex: ALLMin age: 18 YearsMax age: 64 YearsHealthy volunteers:

Medical Language ↔ Plain English

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

Locations (1)

Rowan University School of Osteopathic Medicine

Stratford, New Jersey, United States

Outcomes

Primary Outcomes

Composite measures of walking

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

Time frame: 1 year

Data from ClinicalTrials.gov

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