Modafinil and Exercise for Post Stroke Fatigue

Official title

Modafinil and Exercise for Post Stroke Fatigue (MODEX)

Overview

A stroke happens when blood flow to the brain is stopped and the brain gets damaged. At least half of people with a stroke have fatigue months and even years later. A lot of people report fatigue as one of the worst symptoms post stroke that can affect daily activities and the length and quality of life. Though all the reasons for fatigue after stroke and how to best treat it are not fully understood, the investigators think that fatigue results from the stroke changing the brain, reducing physical fitness, and decreasing muscle strength. A stroke can also affect sleep and mood, which can impact how people feel too. It is also not known why women experience more fatigue than men after a stroke. Some studies have tested a drug called Modafinil for post stroke fatigue, while other studies have tested exercise for it. Yet, there is unclear evidence for either treatment, so this study has the following aim: 1\. Test if Exercise plus Modafinil is better than Exercise plus a Sugar Pill This study will take place at up to 6 Canadian research sites to give a good representation of people after a stroke. Each person will be tested on fatigue, mood, fitness, thinking skills, sleep, and usual activity levels. Participants will be assigned at random (like flipping a coin) to 1 of 2 groups: 1. Sugar Pill plus Exercise 2. Modafinil plus Exercise The treatment will last 8 weeks. The Modafinil or Sugar Pill will be taken once a day. The exercise will be delivered virtually by a trained therapist over computer to people at home 3 times a week. Change in fatigue, quality of life, and other outcomes will be measured over 6 months. The investigators will assess the results to identify the best treatment for post stroke fatigue and hope to be able to find a treatment that will help reduce fatigue and improve quality of life after a stroke.

Detailed description

Study Rationale Post stroke fatigue (PSF) afflicts as many as 70% of the 400,000 Canadians with stroke. People with stroke endorse PSF as the most serious unmet research priority. Pathological fatigue is not relieved by rest and is characterized by persistent or extreme tiredness, exhaustion, and/or difficulty in initiating or sustaining voluntary activities. PSF is an excellent exemplar to study as the cause of disabling PSF is unclear. Systematic reviews confirm that PSF is multifactorial having both peripheral (e.g. cardiovascular and neuromuscular) and central (e.g. alterations in brain function resulting in both physical and psychological symptoms) components. There are no evidence-based treatments for PSF, however, exercise and the dopaminergic medication Modafinil that targets the dopaminergic movement circuits in the brain, have shown promise in alleviating symptoms in small studies.

Study Design This multicentre clinical trial will involve a double blind randomized controlled trial design to quantify the effect of a structured exercise program combined with Modafinil 200 mg daily or placebo medication over 8 weeks on severity of fatigue symptoms. It aims to recruit 212 participants into one of two arms. It will also explore the interactions of Modafinil in combination with exercise. The effects of mood, sleep, stroke impairments, sex, gender and activity levels on post stroke fatigue will also be explored.

Study Population Study participants must meet the inclusion/exclusion criteria at the time of entry into the study. In general, participants will be \>3 months post stroke onset (i.e. intracerebral hemorrhage or ischemic stroke diagnosed by a physician) at the time of consent into the study.

Primary Hypothesis The primary hypothesis based on outcomes at 8 weeks is that structured telerehabilitation fitness and strengthening exercise plus Modafinil will improve fatigue symptom severity more than placebo medication and the same exercise.

Interventions

• Drug Modafinil 200mg
  Modafinil 200mg daily for 8 weeks.
• Drug Placebo
  Placebo daily for 8 weeks.
• Behavioral Exercise
  Exercise three times per week for 8 weeks.

Primary outcome measures

• Severity of Fatigue Symptoms [Time frame: Week 8]

Secondary outcome measures (10)

• Severity of Fatigue Symptoms [Time frame: Week 4 and 26]
• Impact on Quality of Life [Time frame: Week 8 and 26]
• Walking Recovery [Time frame: Week 8 and 26]
• Leg Strength and Coordination [Time frame: Week 8 and 26]
• 3-Day Physical Activity Assessment [Time frame: Week 8]
• Mood and Anxiety [Time frame: Week 4, 8, and 26]
• Attention [Time frame: Week 8 and 26]
• Cognition [Time frame: Week 8 and 26]
• Health Resource Utilization [Time frame: Week 4, 8, and 26]
• Quality Adjusted Life Years [Time frame: Week 4, 8, and 26]

Eligibility criteria

Inclusion criteria

• >18 years of age (on date of consent)
• >3 months post stroke onset (i.e. intracerebral hemorrhage or ischemic stroke diagnosed by a physician) (on date of consent)
• evidence of stroke on computed tomography (CT) or magnetic resonance imaging (MRI)
• disabling post stroke fatigue as measured by Multidimensional Fatigue Inventory score >60
• Modified Rankin disability score <4
• Able to participate in moderate exercise for an hour (with one person assistance or less)

Exclusion criteria

• contraindications to Modafinil
• on stimulant medications already
• subarachnoid hemorrhage
• impaired comprehension or language impairment that prevents following visual or pictograph adapted instructions or providing informed consent
• severe motor impairment or inability to participate in the exercise
• unable to participate in exercise due to musculoskeletal complaints, unstable heart failure, or renal disease
• untreated hypothyroidism or anemia
• cancer likely to result in death in <6 months
• severe depression requiring therapy as indicated by suicidal ideation and/or Depression Anxiety Stress Scales (DASS) depression sub-score >20
• currently enrolled in a structured exercise program
• untreated severe sleep apnea with an Apnea/Hypopnea index >30 as measured by validated wearable sleep apnea detector
• pregnant, breastfeeding, or positive test for pregnancy at baseline

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Quadruple blind

Primary purpose

Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06354985 · 23-5996 · MODEX2023 · FRN:183960 · CTO Project ID: 4701

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗