Exercise Study of Function and Pathology for Women With X-linked Adrenoleukodystrophy
Primary Purpose
X-linked Adrenoleukodystrophy
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
exercise training
Sponsored by
About this trial
This is an interventional treatment trial for X-linked Adrenoleukodystrophy focused on measuring exercise, women, training, rehabilitation, leukodystrophy
Eligibility Criteria
Inclusion Criteria:
- confirmed diagnosis, X-ALD heterozygote carrier
- no medical contraindication to participating in a strength training program
- able to follow complex directions as determined by a score of ≤1 on a subset of questions taken from the NIH Stroke scale (Brott et al. 1989)
- hip flexion strength: 6.6-15.8kg
- hip extension strength: up to 18.3 kg
- normal passive range of motion at hips/knees/ankles
- able to walk ≥50m
Exclusion Criteria:
- Evidence of other neurological deficit that could interfere, such as previous stroke or muscle disease
- congestive heart failure
- cancer
- orthopedic conditions
- severe pain that precludes study participation
- seizures
- pregnancy
- other medical condition that precludes participation in an exercise program, e.g., unstable angina, uncontrolled diabetes, uncontrolled hypertension
Healthy controls have the same age and exclusion criteria as women with AMN except that they will not be carriers for X-ALD. They must have normal neurological function.
Sites / Locations
- Motion Analysis Lab
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
exercise
Arm Description
Female carriers as well as healthy age and gender matched individuals will participate in an exercise paradigm.
Outcomes
Primary Outcome Measures
Change in Maximal Voluntary Contraction of the Hip Flexors From Baseline to End of Training and to Post-training
Here, we will assess whether the degree of a person's white matter integrity (i.e. for tracts of interest as measured from MRI) predicts their ability to benefit from exercise. Our prediction is that those individuals with preserved white matter integrity will show the greatest improvement in hip flexor strength.
Secondary Outcome Measures
Full Information
NCT ID
NCT01594853
First Posted
May 7, 2012
Last Updated
December 14, 2017
Sponsor
Hugo W. Moser Research Institute at Kennedy Krieger, Inc.
Collaborators
European Leukodystrophy Association
1. Study Identification
Unique Protocol Identification Number
NCT01594853
Brief Title
Exercise Study of Function and Pathology for Women With X-linked Adrenoleukodystrophy
Official Title
Exercise Study of Function and Pathology for Women With X-ALD
Study Type
Interventional
2. Study Status
Record Verification Date
December 2017
Overall Recruitment Status
Completed
Study Start Date
May 2012 (undefined)
Primary Completion Date
October 2014 (Actual)
Study Completion Date
October 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hugo W. Moser Research Institute at Kennedy Krieger, Inc.
Collaborators
European Leukodystrophy Association
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose is to see how X-linked adrenoleukodystrophy (X-ALD) is associated with strength and sensation using MRI, in women with X-ALD. The investigators will also see whether exercise can improve these symptoms for women with X-ALD.
Detailed Description
X-linked adrenoleukodystrophy (X-ALD), a [sex-linked] progressive neurodegenerative disease, is caused by a defect in the ABCD1 gene. The disease is expressed in multiple ways, but the most common adult form is adrenomyeloneuropathy (AMN), which results in slowly progressive changes in muscle tone and weakness, sensory loss, and dysfunction of the autonomic nervous system. In a previous study the investigators linked abnormalities in the [brain/spinal cord] to lower extremity weakness in men with AMN; however, there have been no studies evaluating these relationships in women carriers (i.e., women with AMN). It is unknown, in women with AMN, how the pattern of damage in the brain and spinal cord relates to disability and if these patterns predict responsiveness to treatment. The investigators hypothesize that by using magnetization transfer (MT) and diffusion tensor imaging (DTI), two magnetic resonance imaging (MRI) modalities, to track particular changes in the brain and spinal cord will predict disability and additionally, who is likely to respond best to a training regimen. The investigators expect that these more advanced imaging techniques will be more sensitive and accurate quantitative measures of clinical motor function and women with greater loss in the spinal cord compared to the brain will benefit most from training to improve disability. To test this hypothesis, women with AMN will receive MRI scans at baseline and complete measures of global walking and lower extremity impairments of vibration sensation, spasticity, and strength at three time-points: baseline, 12 weeks, and 18 weeks after baseline. The group will participate in a resistive training program for 12 weeks. MRI data will be correlated to changes over time in measures of impairment to determine their relationships. The linking of this information will not only be important for better defining disability in women with AMN but it will also help to guide physicians and rehabilitation therapists in predicting who is likely to respond to rehabilitative interventions, as well as for optimizing the effects of future pharmacological interventions.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
X-linked Adrenoleukodystrophy
Keywords
exercise, women, training, rehabilitation, leukodystrophy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
31 (Actual)
8. Arms, Groups, and Interventions
Arm Title
exercise
Arm Type
Experimental
Arm Description
Female carriers as well as healthy age and gender matched individuals will participate in an exercise paradigm.
Intervention Type
Behavioral
Intervention Name(s)
exercise training
Other Intervention Name(s)
strengthening, Curves
Intervention Description
The exercise program uses a local Curves® gym to provide an individualized program of strength and cardiovascular training. The program is expected to be performed for 45 minutes 4-6 days per week.
Primary Outcome Measure Information:
Title
Change in Maximal Voluntary Contraction of the Hip Flexors From Baseline to End of Training and to Post-training
Description
Here, we will assess whether the degree of a person's white matter integrity (i.e. for tracts of interest as measured from MRI) predicts their ability to benefit from exercise. Our prediction is that those individuals with preserved white matter integrity will show the greatest improvement in hip flexor strength.
Time Frame
Participants are assessed at baseline (visit 1, enrollment), end of training (visit 2, week 12) and post-training (visit 3, week 18).
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
confirmed diagnosis, X-ALD heterozygote carrier
no medical contraindication to participating in a strength training program
able to follow complex directions as determined by a score of ≤1 on a subset of questions taken from the NIH Stroke scale (Brott et al. 1989)
hip flexion strength: 6.6-15.8kg
hip extension strength: up to 18.3 kg
normal passive range of motion at hips/knees/ankles
able to walk ≥50m
Exclusion Criteria:
Evidence of other neurological deficit that could interfere, such as previous stroke or muscle disease
congestive heart failure
cancer
orthopedic conditions
severe pain that precludes study participation
seizures
pregnancy
other medical condition that precludes participation in an exercise program, e.g., unstable angina, uncontrolled diabetes, uncontrolled hypertension
Healthy controls have the same age and exclusion criteria as women with AMN except that they will not be carriers for X-ALD. They must have normal neurological function.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kathleen M Zackowski, Ph.D.
Organizational Affiliation
Hugo W. Moser Research Institute at Kennedy Krieger, Inc.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Motion Analysis Lab
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21205
Country
United States
12. IPD Sharing Statement
Links:
URL
http://www.kennedykrieger.org/research-training
Description
See Clinical Research Projects listing.
Learn more about this trial
Exercise Study of Function and Pathology for Women With X-linked Adrenoleukodystrophy
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