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Treating Restless Leg Syndrome in Women with ALD - Part 1

Studio in corso
Arruolamento in corso
PHASE 1:
In Phase 1 of this research study, we want to learn more about how common restless legs syndrome (RLS) is in women with X-linked adrenoleukodystrophy (ALD). You may be eligible to take part in Phase 1 of the study if you have been diagnosed with ALD and are a female age 18 years and older. We anticipate that 50 people at Massachusetts General Hospital (MGH) and 50 people at the University Medical Center (UMC) of Amsterdam will participate in Phase 1 of the study. Participation in Phase 1 may include the following visits:
ALD Eligibility Remote Pre-Screening Visit (V1): This visit will be conducted over the phone with a study coordinator. It will consist of a review of medical and demographic history to determine if you are eligible to participate in the study.
RLS Diagnostic Remote Visit (V2): Eligible patients will be interviewed by both an expert in ALD (Dr. Florian Eichler) and an expert in RLS (Dr. John Winkelman) to determine if you have any symptoms of RLS. This visit will also involve completion of a series of questionnaires including the following: The 12-Item Multiple Sclerosis Walking Scale (MSWS-12), Spasticity Screening Tool, The Generalized Anxiety Disorder Assessment (GAD-7), The Patient Health Questionnaire (PHQ-9), and The 36-Item Short Form Survey (SF-36).
RLS Severity Remote Visit (V3): Patients who meet the diagnostic criteria for RLS will undergo an additional telephone interview with Dr. Eichler or Dr. Winkelman to determine the severity of RLS symptoms.
Obiettivi
Durata dello studio:
23 mois
Inizio dello studio:
marzo 2023
Fine dell’arruolamento:
gennaio 2025
Fine dello studio:
gennaio 2025
Stato
  • Autorizzato in Stati Uniti, Paesi Bassi
  • Arruolamento dei pazienti in corso in Stati Uniti, Paesi Bassi
Criteri d’inclusione
  • Age : greater than or equal to 18 years
  • Sex : female
  • To have one of the following pathologies : X-linked Adrenoleukodystrophy / ALD (ABCD1), Adrenomyeloneuropathy / AMN
  • Subject : patient
Soddisfo tutti i criteri d’inclusione
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Sede dello studio
  • MGH, Boston, Stati Uniti
  • Amsterdam UMC, Amsterdam, Paesi Bassi
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