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Adderall XR and Processing Speed in Multiple Sclerosis (MS)

Phase 2
Completed
Conditions
Multiple Sclerosis
Cognitive Impairment
Impaired Processing Speed
Interventions
Registration Number
NCT01667484
Lead Sponsor
London Health Sciences Centre
Brief Summary

Cognitive impairment, or problems with thinking and memory, is common in multiple sclerosis (MS) and can occur independently of physical disability. It is the most common reason, along with physical fatigue, for MS patients to stop working. The most frequent complaint is problems with multi-tasking or thinking quickly, which corresponds to impairment in the cognitive domain of processing speed. Currently there is treatment available to prevent relapses and physical disability but there are no medications that have been shown to treat cognitive impairment. Amphetamines have been beneficial for selective attention and processing speed in attention deficit hyperactivity disorder (ADHD) and traumatic brain injury. This is study will determine whether Adderall XR improves objective measures of processing speed and attention in MS patients impaired in this cognitive domain, by comparing two doses of Adderall XR (5 and 10mg) to placebo before and after the medication is administered. The results of this study will help provide data to design a larger study to determine if Adderall XR, and potentially other amphetamine drugs, will help treat cognitive impairment in MS patients.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
70
Inclusion Criteria
    • Males/Females who are ≥ 18 years old and ≤ 59 years old
  • Relapsing Remitting, Secondary Progressive or Primary Progressive MS, as per revised McDonald's Criteria
  • Have not received corticosteroids in last thirty days or a relapse in the last ninety days
  • An Expanded Disability Status Scale (EDSS) of ≤ 6.5
  • If female, must neither be pregnant nor breast-feeding
Exclusion Criteria
    • Have evidence of other medical cause(s) of cognitive impairment
  • Have evidence of major depression as determined by a positive Beck Depression Index-Fast screen ≥ 13and/or by clinician interview or evidence of severe fatigue with a Fatigue Severity Scale ≥ 5.

  • Have demonstrated a hypersensitivity to amphetamines in the past

  • Have uncontrolled or labile hypertension (> 135/85 mm Hg, treated or untreated)

  • Have a history of structural heart disease, including atherosclerosis or angina

  • Have a diagnosis of bipolar disorder or a history of a psychotic episode

  • The following medications are not permitted to be used within 14 days the study

    1. Monoamine Oxidase Inhibitors
    2. Sympathomimetics or methadone
    3. Antipsychotic agents
    4. Modafinil
  • The following medications are permitted if the dose has been stable for ≥ 28 days

    1. Short acting benzodiazepines, qhs administration only
    2. Anticonvulsants, including gabapentin and pregabalin
    3. Bupropion
    4. Tricyclic Antidepressants
    5. Anti-spasmodics such as baclofen or tizanidine
    6. Anticholinergic medication
    7. Selective serotonin(-norepinephrine) reuptake inhibitors

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PlaceboPlacebotreatment group #1
Adderal XR 10mgAdderall XR 10 mgtreatment group #3
Adderall XR 5mgAdderall XR 5mgtreatment group #2
Primary Outcome Measures
NameTimeMethod
Change in score of Paced Auditory Serial Addition Test (PASAT)pre and 7 hours post dose

measure of processing speed

Change in Score of Symbol Digit Modalities Test (SDMT)pre and 7 hours post dose

measure of processing speed

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

London Health Sciences Center and St. Joseph's Heathcare Center (Parkwood)

🇨🇦

London, Ontario, Canada

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