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Adderall XR and Processing Speed in Multiple Sclerosis (MS)

Does Adderall XR Improve Processing Speed in Cognitively Impaired MS Patients?

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01667484
Enrollment
70
Registered
2012-08-17
Start date
2012-09-30
Completion date
2015-02-28
Last updated
2015-05-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Impairment, Impaired Processing Speed, Multiple Sclerosis

Keywords

Cognitive Impairment, Multiple Sclerosis, Processing Speed, Treatment

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.

Interventions

DRUGAdderall XR 5mg
DRUGAdderall XR 10 mg
DRUGPlacebo

Sponsors

London Health Sciences Centre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 59 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change in score of Paced Auditory Serial Addition Test (PASAT)pre and 7 hours post dosemeasure of processing speed
Change in Score of Symbol Digit Modalities Test (SDMT)pre and 7 hours post dosemeasure of processing speed

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026