Task Specific Training for Advanced Multiple Sclerosis

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorHunter College of City University of New York

About this trial

The purpose of this study is to find effective physical therapy treatments for individuals who have severe multiple sclerosis. Physical therapy treatments for mild-to-moderate multiple sclerosis exists, however, very limited research has been done for physical therapy for severe multiple sclerosis (MS). In this study 10 participants diagnosed with severe MS will engage in 1-hour physical therapy sessions twice a week for 6 weeks to address limitations in standing, balancing, and bed mobility.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

definitive diagnosis of Multiple Sclerosis

Expanded Disability Status Scale (EDSS) of 7.0-8.0

Ability to read, understand , and sign an informed consent -

Disqualifiers

evidence of MS exacerbation in the 4 weeks prior to starting the study

any orthopedic, cardiopulmonary, or non-MS neurologic symptoms that will interfere with their ability to participate in the study

Trial design

Design model

Single group

Treatments tested in this trial

  • Task specific physical therapy

    Other intervention

    Physical Therapy based specifically on tasks that the participant os having difficulty with

Treatment groups

15 Participants
are divided into 1 treatment group
Group A: Task specific Physical TherapyExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Multiple Sclerosis Physical Frailty Functional Assessment (MSPFFA)

Assessment of ability to perform functional mobility tasks. The MSPFFA is a 14 item ordinal scale; the maximum score is a 56, minimom score is 14. The higher the score, the better the function and the less physically frail the person being tested is considered to be.

Time frame
Will be administered twice, once at pre-intervention and once at post-intervention. The length of the intervention is 6 weeks.

Secondary outcomes

1

Multiple Sclerosis Impact Scale-29 (MSIS29)

Self report measure of the impact of MS on the participant. The MSIS-29 is 29 item self report measure. The higher the score, the greater the impact of MS on the person person reporting bleives they have.The score is rated from 0-100 with the higher score indicating a greater impact on the individual from MS.

Time frame
Will be administered twice, once at pre-intervention and once at post-intervention. The length of the intervention is 6 weeks.

Other outcomes

Sponsors and contacts

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Hunter College of City University of New York

Lead sponsor

Multiple Sclerosis Foundation

Collaborator