Fatigue Clinical Trial
Official title:
A Placebo-controlled Double Blind Crossover Trial of Acetylsalicylic Acid as a Pre-treatment for Exercise in Multiple Sclerosis
Verified date | November 2018 |
Source | Columbia University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Exercise has many benefits for people with multiple sclerosis (MS), such as improved physical
symptoms, mood, fatigue, and cognition. However, many people with MS refrain from exercising
because of the discomfort of exhaustion and overheating that they experience. This study
investigates the use of aspirin before exercise as a treatment to reduce overheating and
exhaustion, thereby availing many more people with MS the opportunity to benefit from
exercise.
The investigators recently published the first-ever report of elevated body temperature in
relapsing-remitting MS (RRMS) patients relative to healthy controls, and elevated temperature
was linked to worse fatigue. This finding that body temperature is elevated and linked to
fatigue in RRMS lays the groundwork for a paradigm shift in our understanding and treatment
of fatigue. That is, the focus shifts from exogenous to endogenous temperature, and from
stimulant medication to cooling treatments.
A recent study comparing healthy adults to adults with MS showed that whereas exercise
increased body temperature in both groups, only in the MS group was it correlated with
exhaustion. The reason for this may relate to the elevation in resting body temperature in
relapsing-remitting MS (RRMS) patients relative to healthy controls. The finding is
clinically meaningful, as elevated body temperature was correlated with worse fatigue in
patients. Exercise Aim: To determine whether pretreatment with ASA (compared to placebo:
within subject crossover design) before exercise results in improved exercise performance
(i.e., increased time-to-exhaustion). The investigators hypothesize that participants will
tolerate exercise for longer after taking ASA than placebo. This hypothesis is based on a)
demonstrated efficacy of antipyretic for reducing body temperature during exercise in healthy
controls, b) demonstrated efficacy of antipyretic for reducing fatigue in non-exercising MS
patients, and c) demonstrated efficacy of elaborate (unblinded) cooling treatments (e.g.,
cooling garments, cooling hand chamber) for improving exercise performance in MS patients.
Note that this project is especially important for MS patients, who have a disease-specific
body temperature elevation and sensitivity to heat (i.e., Uhthoff's).
Status | Completed |
Enrollment | 12 |
Est. completion date | May 10, 2017 |
Est. primary completion date | May 10, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility |
Inclusion Criteria: - RRMS - self report of overheating during exercise - low physical disability (EDSS total score 4.5 or less); fully ambulatory without aid - exacerbation-free (and no use of corticosteroids) for 6 weeks prior - BMI 35 or lower Exclusion Criteria: - uncontrolled hypertension or vascular disease of the legs - current medications for heart or blood pressure problem - prior history of head injury, stroke, or other neurological disease/disorder - currently taking antipyretics or pain medication daily - presence of major depressive disorder or other psychiatric diagnosis - formally diagnosed sleep disorder - pulmonary disease, heart disease or other heart problem - diabetes mellitus or problem with blood sugar levels - lower body weakness or reliance on supportive devices for walking (as indicated through EDSS) - counter indications to aspirin use: history of confirmed peptic ulcer, gastrointestinal or sever gynecological bleeding; tarry stool or fecal occult blood; syndrome of asthma, rhinitis or nasal polyps |
Country | Name | City | State |
---|---|---|---|
United States | Columbia University Medical Center, MS Center | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Columbia University | National Multiple Sclerosis Society |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Time to Exhaustion | The measure of interest is the length of time (in seconds) spent exercising at each session. This time has no pre-set upper limit, i.e. patients are free to exercise as long as they wish. This means that the time will not be censored. However, please note that healthy adults' time to exhaustion is approximately 12 minutes. | ASA's effect will be assessed from date of randomization until cessation of exercise test at each of two study visits to be completed within a 14-day period. | |
Secondary | Exercise-induced Body Temperature Increase | Measure of interest is increase in body temperature from pre- to post-exercise test in each treatment condition (ASA vs. placebo) | Effect of treatment on body temperature in a single session (i.e., pre- to post- exercise test) to be completed within a 14-day period |
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