Maybe you want modafinil for this use:
Systematic review shows ‘smart drug’ modafinil does enhance cognition
or this:
Effects of modafinil on non-verbal cognition, task enjoyment and creative thinking in healthy volunteers
Modafinil May Alleviate Poststroke Fatigue
A Randomized, Placebo-Controlled, Double-Blinded Trial
- Mai Bang Poulsen, MD;
- Bodil Damgaard, MD;
- Bo Zerahn, MD;
- Karsten Overgaard, MD;
- Rune Skovgaard Rasmussen, MA, PhD
+ Author Affiliations
- Correspondence to Mai Bang Poulsen, MD, Department of Neurology, Herlev Hospital, Herlev Ringvej 75, 2730 Herlev, Denmark. E-mail maibang@gmail.com
Abstract
Background and Purpose—Poststroke
fatigue is common and reduces quality of life. Current evidence for
intervention is limited, and this is the first
placebo-controlled trial to investigate
treatment of poststroke fatigue with the wakefulness promoting drug
modafinil.
Methods—The trial
was randomized, double-blinded, and placebo-controlled. Patients were
treated with 400-mg modafinil or placebo for
90 days. Assessments were done at inclusion,
30, 90, and 180 days. The primary end point was fatigue at 90 days
measured by
the Multidimensional Fatigue Inventory-20
general fatigue domain. Secondary end points included the Fatigue
Severity Scale,
the Montreal Cognitive Assessment, the
modified Rankin Scale and the Stroke-specific quality of Life
questionnaire. Adult
patients with a recent stroke achieving a
score of ≥12 on the Multidimensional Fatigue Inventory-20 general
fatigue domain
were consecutively included. Exclusion
criteria were severe cognitive disabilities and contraindications for
modafinil treatment.
Results—One
thousand one hundred twenty-one patients with stroke were screened and
41 patients included, 21 received modafinil. The
primary end point, the Multidimensional
Fatigue Inventory-20 general fatigue score, did not differ between
groups. Patients
in the modafinil group obtained better scores
on the Fatigue Severity Scale (P=0.02) and in some subscales of the stroke-specific quality of life questionnaire (0.001<P<0.05),
which were secondary outcomes. No serious adverse reactions were
observed and there was no difference in blood pressure
between groups.
Conclusions—There
were no significant differences between the 2 groups with regard to the
primary end point. There were secondary significant
outcomes that should be explored in future
trials.
Clinical Trial Registration—URL: http://www.clinicaltrials.gov. Unique identifier: NCT01800097.
No comments:
Post a Comment