Dalfampridine for Imbalance in Multiple Sclerosis
Primary Purpose
Multiple Sclerosis, Fatigue
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Dalfampridine
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Multiple Sclerosis focused on measuring multiple sclerosis, postural balance, gait, fatigue
Eligibility Criteria
Inclusion Criteria:
- Age 20- 59 years,
- Able to walk at least 100m without an aide or with unilateral assistance
- Prolonged APR latencies (≥ 1SD > mean for healthy people in this age range) OR,
- Reduced balance-related activity (ABC scores ≤ 85%),
- Abnormal trunk range of motion (horizontal), trunk range of motion (frontal), turning duration, cadence, double support time, stride length or gait cycle time (outside 1SD of the average for healthy people in this age range)
Exclusion Criteria:
- Currently taking dalfampridine (any within the last 2 weeks),
- Cause(s) of imbalance other than MS,
- Impaired renal function (creatinine clearance ≤50mL/min),
- Seizure disorder
- Pregnancy or breast feeding
Sites / Locations
- Oregon Health and Science University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Dalfampridine
Placebo
Arm Description
Outcomes
Primary Outcome Measures
Change in Automatic Postural Response (APR )Latency
Automatic Postural Response (APR) latencies will be measured by Computerized Dynamic Posturography (CDP). The restoration of balance after an unexpected movement by Computerized Dynamic Posturography relies on automated postural responses in the upper and lower legs, trunk, shoulders, and neck muscles. APR latency is the reaction- time response to movements of the support surface on which the subject stands. These responses typically occur at onset latencies of ~100 milliseconds. In response to a change, both feet-in-place and stepping strategies can be used to recover balance, with the incidence of stepping responses becoming larger as the change magnitude increases voluntary movements in human subjects.
Secondary Outcome Measures
Change in Activities-specific Balance Confidence (ABC) Questionnaire Scores
The ABC is an 11-point scale and subjects are asked to indicate personal level of confidence in doing specific activities without losing balance or becoming unsteady on a scale from 0% to 100%. The ratings are added (possible range =0 -1600) and divide by 16 to get each subject's ABC score. A high ABC score indicates a high degree of confidence and a low ABC score indicates a low degree of confidence.
Change in Timed 25 Foot Walking Speed
Full Information
NCT ID
NCT01444300
First Posted
September 20, 2011
Last Updated
May 16, 2014
Sponsor
Oregon Health and Science University
Collaborators
Acorda Therapeutics
1. Study Identification
Unique Protocol Identification Number
NCT01444300
Brief Title
Dalfampridine for Imbalance in Multiple Sclerosis
Official Title
Dalfampridine to Improve Imbalance in Multiple Sclerosis: A Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
May 2014
Overall Recruitment Status
Completed
Study Start Date
September 2011 (undefined)
Primary Completion Date
September 2013 (Actual)
Study Completion Date
September 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oregon Health and Science University
Collaborators
Acorda Therapeutics
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Dalfampridine is a new medication that was FDA approved in 2010 to improve walking speed in people with Multiple Sclerosis (MS). People with MS walk slowly in part because MS damages the myelin insulation around nerves which slows conduction of messages from the brain to the leg muscles. Dalfampridine works by improving conduction in nerves with damaged myelin. Recent research indicates that imbalance in MS is in large part caused by poor conduction by the nerves that transmit information about the position of the legs to the brain. It is therefore likely that, by improving nerve conduction, dalfampridine will also improve imbalance in people with MS. Dalfampridine will be administered in this study by the same route (oral), dosage (10mg), and frequency (every 12 hours) approved by the FDA to improve walking speed in people with MS. The proposed pilot study will examine the effects of dalfampridine on imbalance in 24 subjects with Multiple Sclerosis (MS) and imbalance. This small pilot study will help to show if dalfampridine improves imbalance in MS and will guide the design and implementation of a larger full scale study to definitively determine if dalfampridine improves balance and prevents falls in people with MS.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis, Fatigue
Keywords
multiple sclerosis, postural balance, gait, fatigue
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
24 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Dalfampridine
Arm Type
Experimental
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Dalfampridine
Other Intervention Name(s)
Ampyra
Intervention Description
10mg, bid, pill taken by mouth for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
placebo pill, bid for 12 weeks
Primary Outcome Measure Information:
Title
Change in Automatic Postural Response (APR )Latency
Description
Automatic Postural Response (APR) latencies will be measured by Computerized Dynamic Posturography (CDP). The restoration of balance after an unexpected movement by Computerized Dynamic Posturography relies on automated postural responses in the upper and lower legs, trunk, shoulders, and neck muscles. APR latency is the reaction- time response to movements of the support surface on which the subject stands. These responses typically occur at onset latencies of ~100 milliseconds. In response to a change, both feet-in-place and stepping strategies can be used to recover balance, with the incidence of stepping responses becoming larger as the change magnitude increases voluntary movements in human subjects.
Time Frame
Baseline to 12 weeks
Secondary Outcome Measure Information:
Title
Change in Activities-specific Balance Confidence (ABC) Questionnaire Scores
Description
The ABC is an 11-point scale and subjects are asked to indicate personal level of confidence in doing specific activities without losing balance or becoming unsteady on a scale from 0% to 100%. The ratings are added (possible range =0 -1600) and divide by 16 to get each subject's ABC score. A high ABC score indicates a high degree of confidence and a low ABC score indicates a low degree of confidence.
Time Frame
Baseline to 12 weeks
Title
Change in Timed 25 Foot Walking Speed
Time Frame
Baseline to 12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
59 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 20- 59 years,
Able to walk at least 100m without an aide or with unilateral assistance
Prolonged APR latencies (≥ 1SD > mean for healthy people in this age range) OR,
Reduced balance-related activity (ABC scores ≤ 85%),
Abnormal trunk range of motion (horizontal), trunk range of motion (frontal), turning duration, cadence, double support time, stride length or gait cycle time (outside 1SD of the average for healthy people in this age range)
Exclusion Criteria:
Currently taking dalfampridine (any within the last 2 weeks),
Cause(s) of imbalance other than MS,
Impaired renal function (creatinine clearance ≤50mL/min),
Seizure disorder
Pregnancy or breast feeding
Facility Information:
Facility Name
Oregon Health and Science University
City
Portland
State/Province
Oregon
ZIP/Postal Code
97239
Country
United States
12. IPD Sharing Statement
Links:
URL
http://www.ohsu.edu/ms
Description
OHSU Multiple Sclerosis Center
Learn more about this trial
Dalfampridine for Imbalance in Multiple Sclerosis
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