Treating Leg Symptoms in Women With X-linked Adrenoleukodystrophy

Restless Legs Syndrome Clinical Trial

Official title:

Treating Leg Symptoms in Women With X-linked Adrenoleukodystrophy: A Key to Improving Sleep and Gait Performance

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05003648
• Other study ID #: 2021P001543
• Status: Recruiting
• Phase: Phase 4
• Start date: April 1, 2023
• Est. completion date: November 1, 2025

Study information

• Verified date: April 2024
• Source: Massachusetts General Hospital
• Contact: Riya Saxena
• Phone: 603-674-6743
• Email: rsaxena2[@]mgh.harvard.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The investigators recently observed that up to 25% of women with X-linked adrenoleukodystrophy (ALD) have moderate to severe Restless Leg Syndrome (RLS). In this study, the investigators aim to estimate the prevalence of RLS among women with ALD and to assess whether pramipexole improves RLS symptoms as well as sleep and gait measures in women with ALD.

Description:

X-linked adrenoleukodystrophy (ALD) is a neurodegenerative disease caused by mutations in the ABCD1 peroxisomal half-transporter gene, resulting in accumulation of very long chain fatty acids (VLCFAs). As ALD is an X-linked disease, women were previously considered asymptomatic carriers. It is now known that even though adrenal insufficiency and cerebral disease occur in less than 1% of women, more than 80% eventually develop progressive spinal cord disease. Recently, the investigators observed that women are more frequently affected by movement disorders independent of the demyelinating brain disease seen in men. In a pilot study, the investigators found that up to 25% of women with ALD have moderate to severe Restless Leg Syndrome (RLS). RLS is a movement disorder characterized by a powerful urge to move the legs, usually accompanied by unpleasant dysesthesias, that is precipitated by rest, relieved by movement, and most pronounced in the evening or at night. Dopamine agonists such as pramipexole are efficacious and first-line FDA-approved treatments in low doses for primary (i.e., idiopathic) RLS and have been shown to improve both the primary symptoms of RLS (sensory discomfort, motor restlessness) as well as the associated sleep and quality of life impairments in RLS. In the first phase of the study, the investigators will enroll 100 women with ALD at the two participating sites (Massachusetts General Hospital and University Medical Center Amsterdam). Participants will undergo structured phone interviews with both an expert in ALD and RLS to assess the presence of probable or definite RLS. Participants with probable or definite RLS will then undergo an additional phone call to determine RLS severity and assess eligibility for the second phase of the study. The objective of the first phase of the study is to determine the prevalence of RLS in women with ALD. The second phase of the study will consist of a 4-month randomized, double-blind, placebo-controlled cross over study to assess whether pramipexole improves RLS symptoms as well as sleep and gait measures in women with ALD. The investigators will enroll 24 women with ALD and moderate to severe RLS. Participants will first be randomized 1:1 to 0.125-0.5 mg pramipexole or placebo. After the first two months, a switch-over visit will take place and include a battery of neurological assessments, walking measures, polysomnography, and questionnaires. At this visit, the crossover from pramipexole to placebo and from placebo to pramipexole will occur. The final study visit will occur 2 months after the switch-over visit and all study assessments will be repeated.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 24
• Est. completion date: November 1, 2025
• Est. primary completion date: April 1, 2025
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 75 Years

Eligibility

PHASE 1 (PREVALENCE STUDY)

Inclusion Criteria:

1. Women of any ethnic origin.

2. Ability to provide verbal consent

3. A willingness and ability to comply with study procedures.

4. Age 18-75 years

5. Metabolically or genetically confirmed diagnosis of ALD

Exclusion Criteria:

1. Inflammatory brain demyelination PHASE 2 (CROSS-OVER STUDY)

Inclusion Criteria:

1. Participation in Phase 1

2. Ability to provide written informed consent

3. Women with ALD who have Restless Leg Syndrome (IRLS > 15)

Exclusion Criteria:

1. Pregnant. Research staff perform pregnancy tests upon visit to center.

2. Participants with active or unstable major psychiatric disorder other than ALD, who, in the investigators' judgement, require further treatment

3. Use of dopaminergic agonists or antagonists within the last 30 days

4. Alcohol use disorder within the last 30 days

5. History of being treated for restless legs syndrome, specifically with dopamine agonist medications

6. Methamphetamine or benzodiazepine dependence in the last 30 days

7. Neurological disorder or cardiovascular disease raising safety concerns about use of pramipexole and/or judged to interfere with ability to assess efficacy of the treatment

8. Medical instability considered to interfere with study procedures

9. Renal disease judged to interfere with drug metabolism and excretion

Related Conditions & MeSH terms

• Adrenoleukodystrophy
• Restless Legs Syndrome

Intervention

Drug:
• Pramipexole
Participants will be started on 0.125 mg pramipexole for the first week. If this dose is well tolerated but not effective, the dose can be increased to 0.25 mg for the following week. If this dose is well tolerated but not effective, the dose can be further increased to 0.5 mg for the remainder of the 2-month period.
• Placebo
Matching placebo

Locations

Country	Name	City	State
Netherlands	University Medical Center of Amsterdam	Amsterdam
United States	Massachusetts General Hospital	Boston	Massachusetts

Sponsors (2)

Lead Sponsor	Collaborator
Massachusetts General Hospital	European Leukodystrophy Association

Countries where clinical trial is conducted

United States,  Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in the International Restless Legs Severity (IRLS) score	Change in IRLS score before and after pramipexole treatment. Scores range from 0 to 40, with higher scores representing more severe RLS symptoms.	pre-intervention, week 8, week 17
Primary	Prevalence of Restless Leg Syndrome in Women with X-linked Adrenoleukodystrophy	The prevalence of RLS in women with ALD will be assessed using the Hening Telephone Diagnostic Interview (HTDI), an objective tool to diagnose RLS.	pre-intervention
Secondary	Change in the 36-Item Short Form Survey (SF-36) score	Change in SF-36 score before and after pramipexole treatment. Scores range from 0 to 100, with higher scores representing better quality of life.	pre-intervention, week 8, week 17
Secondary	Change in the Generalized Anxiety Disorder Assessment (GAD-7) score	Change in GAD-7 score before and after pramipexole treatment. Scores range from 0 to 21, with higher scores representing more severe levels of anxiety.	pre-intervention, week 8, week 17
Secondary	Change in the Patient Health Questionnaire (PHQ-9) score	Change in the PHQ-9 score before and after pramipexole treatment. Scores range from 0 to 27, with higher scores representing more severe depression.	pre-intervention, week 8, week 17
Secondary	Improvement in RLS symptoms measured by the Clinical Global Impression - Improvement (CGI-I) scale	Improvement in the patient's illness after pramipexole treatment as determined by the physician. Scores range from 1 (very much improved) to 7 (very much worse).	week 8 and week 17
Secondary	Change in the Expanded Disability Status Scale (EDSS) score	Change in EDSS score before and after pramipexole treatment. Scores range from 0 (no disability) to 10 (death).	pre-intervention, week 8, week 17
Secondary	Change in the Multiple Sclerosis Walking Scale (MSWS-12) score	Change in MSWS-12 score before and after pramipexole treatment. Scores range from 0 to 100, with higher scores representing more severe walking impairment.	pre-intervention, week 8, week 17
Secondary	Change in the Suggested Immobilization Test (SIT)	Change in the sensory and motor aspects of RLS before and after pramipexole treatment, assessed using the SIT.	pre-intervention, week 8, week 17
Secondary	Change in sleep/wake parameters measured by actigraphy	Change in sleep/wake parameters including Total Sleep time, Sleep Latency, and Wake after Sleep Onset before and after pramipexole treatment. Parameters will be objectively measured using wrist-worn actigraphy.	pre-intervention, week 8, week 17
Secondary	Change in the Utah Early Neuropathy Scale (UENS) score	Change in UENS score before and after pramipexole treatment. Scores range from 0 to 42, with higher scores representing more severe neuropathy.	pre-intervention, week 8, week 17
Secondary	Change in the Timed Up and Go (TUG) Test	Change in the amount of time it takes for the patient to get up from an armchair, walk 3 m, turn around, walk back, and sit down again before and after pramipexole treatment. Higher scores represent more severe balance impairment.	pre-intervention, week 8, week 17
Secondary	Change in the 6 Minute Walk (6MW) Test	Change in the maximum distance a patient can walk in 6 minutes before and after pramipexole treatment. Higher scores represent better walking ability.	pre-intervention, week 8, week 17
Secondary	Change in quality of sleep and leg movements per hour of sleep measured by Polysomnography	Change in quality of sleep and indices of periodic leg movements before and after pramipexole treatment. These variables will be assessed using Polysomongraphy and will be measured at the Boston site only.	pre-intervention, week 8, week 17
Secondary	Change in the 13-item Spasticity Screening Tool score	Change in the Spasticity Screening Tool before and after pramipexole treatment. Scores range from 0 to 52, with higher scores representing more severe spasticity symptoms.	pre-intervention, week 8, week 17