Body-weight Supported Treadmill Training in Primary Progressive Multiple Sclerosis: A Pilot Trial
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Multiple Sclerosis
- Sponsor
- Hicks, Audrey, Ph.D.
- Enrollment
- 6
- Locations
- 1
- Primary Endpoint
- Change from baseline in Multiple Sclerosis Functional Composite (MSFC) at 12, 24 and 36 weeks
- Status
- Completed
- Last Updated
- 15 years ago
Overview
Brief Summary
This study is a pilot trial to evaluate the effects of supported treadmill walking in patients with primary progressive multiple sclerosis (MS) on functional and psychosocial outcomes. Patients will exercise three times per week over the course of 6 months and will be evaluated at baseline, 12 weeks and 24 weeks into the program. Follow-up testing will also be conducted 12 weeks after participants have stopped exercising to determined the lasting effects of the intervention.
The investigators hypothesize that supported treadmill walking will be effective at improving physical physical function and psychosocial outcomes in patients with primary progressive MS.
Detailed Description
The use of exercise as an adjunct to other disease modifying treatments in MS has found increasing support over the past decade. There is ample evidence that exercise therapy can improve physical measures of disability in MS, in addition to being safe and well-tolerated. However, there is a paucity of data on whether exercise is equally effective for those with primary progressive MS as it is in relapsing remitting MS. In addition, studies of exercise therapy have traditionally excluded MS patients with severe disability. There are also currently no treatments for primary progressive MS, so finding a safe disease-modifying therapy is of the utmost importance. The investigators are therefore conducting a pilot trial to evaluate the effects of exercise in the form of supported treadmill walking for patients with primary progressive MS with severe functional impairments. Six patients with primary progressive MS with high disability level will be recruited to participate in this study. Participants will exercise using body-weight supported treadmill training (BWSTT; Woodway Loco-system) which allows a portion of an individual's body-weight to be counterbalanced by an overhead pulley system. This system allows patients with limited mobility to walk upright on the treadmill with therapist assistance. Therapists trained in using the BWSTT system will guide the patients' legs through a proper gait motion and assist with lower limb control. Participants will complete 72 training sessions (30min/session, 3x/week) over the course of 24 weeks. Participants will be evaluated at baseline, 12 weeks (half-way through the training program) and 24 weeks (end of intervention). A follow-up assessment will also be performed 12 after participants have completed the training program (36 weeks). Outcome measures are described below.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Signed, written informed consent
- •Males or non-pregnant females, 18-60 years of age (inclusive)
- •Clinically definite PPMS as per the diagnostic criteria of Thompson et al (2000)
- •Expanded disability status score 5.0-8.0 (constant assistance required)
- •Body weight \<90kg (due to support limitations of treadmill)
- •Approval from physician to participate in the exercise program
- •Ability to tolerate upright locomotion of the body weight supported treadmill
- •Ability to visit the different sites required for the study
- •Ability to commit to 3 weekly training sessions for the duration of 24 weeks
Exclusion Criteria
- •Any disability acquired from trauma or another illness that could interfere with evaluation of disability due to MS
- •Any other serious medical condition that might impair the subject's ability to walk on a treadmill and/or participate in aerobic exercise (including but not limited to: documented heart disease or unstable angina, uncontrolled cardiac dysrhythmia, chronic obstructive lung disease, recent non-traumatic fracture, osteoporosis and severe skin ulcerations)
- •Female patients who do not agree to use effective contraceptive method(s) during the study
- •Current use or use within the last 2 months of any on- or off-label disease-modifying therapy including IFN-β, glatiramer acetate, IV steroids, mitoxantrone, azathioprine, and cyclophosphamide
- •Previous experience with supported treadmill training
- •Kidney disease, peripheral vascular disease or poor circulation
- •Inability to undergo MRI or MRI with gadolinium administration
Outcomes
Primary Outcomes
Change from baseline in Multiple Sclerosis Functional Composite (MSFC) at 12, 24 and 36 weeks
Time Frame: Repeat assessments: baseline, 12 weeks, 24 weeks and 36 weeks (12 weeks post-exercise follow-up)
The MSFC assesses functional ability with three scales: the 25ft walk (leg strength and ambulation), the 9-hole peg test (arm strength and coordination) and the Paced Auditory Serial Addition Test (PASAT; cognition). Scores on all three measures are combined to produce a composite Z-score.
Secondary Outcomes
- Change from baseline in Modified Fatigue Impact Scale (MFIS) at 12, 24 and 36 weeks(Repeat assessments: baseline, 12 weeks, 24 weeks and 36 weeks (12 weeks post-exercise follow-up))
- Change from baseline in brain-derived neurotrophic factor (BDNF) at 12, 24 and 36 weeks(Repeat assessments: baseline, 12 weeks, 24 weeks and 36 weeks (12 weeks post-exercise follow-up))
- Change from baseline in Expanded Disability Status Scale (EDSS) at 12, 24 and 36 weeks(Repeat assessments: baseline, 12 weeks, 24 weeks and 36 weeks (12 weeks post-exercise follow-up))
- Change from baseline in Multiple Sclerosis Quality of Life-54 questionnaire at 12, 24 and 36 weeks(Repeat assessments: baseline, 12 weeks, 24 weeks and 36 weeks (12 weeks post-exercise follow-up))
- Change from baseline in magnetic resonance imaging (MRI) outcomes at 24 weeks(Repeat assessments: baseline and 24 weeks)