Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Monday, August 19, 2013

Effect of a Foot-Drop Stimulator and Ankle–Foot Orthosis on Walking Performance After Stroke: A Multicenter Randomized Controlled Trial

Read the last line. But your therapist probably already figured that out.
http://nnr.sagepub.com/content/27/7/579.abstract
  1. Dirk G. Everaert, PhD1
  2. Richard B. Stein, DPhil1
  3. Gary M. Abrams, MD2
  4. Alexander W. Dromerick, MD3
  5. Gerard E. Francisco, MD4
  6. Brian J. Hafner, PhD5
  7. Thy N. Huskey, MD6
  8. Michael C. Munin, MD7
  9. Karen J. Nolan, PhD8,9
  10. Conrad V. Kufta, MD10
  1. 1University of Alberta, Edmonton, Alberta, Canada
  2. 2University of California, San Francisco, CA, USA
  3. 3National Rehabilitation Hospital and Georgetown University, Washington, DC, USA
  4. 4University of Texas Health Sciences Center and TIRR Memorial Hermann, Houston, TX, USA
  5. 5University of Washington, Seattle, WA, USA
  6. 6Washington University in St. Louis, St. Louis, MO, USA
  7. 7University of Pittsburgh, Pittsburgh, PA, USA
  8. 8Kessler Foundation Research Center, West Orange, NJ, USA
  9. 9UMDNJ–New Jersey Medical School, Newark, NJ, USA
  10. 10Innovative Neurotronics, Inc, Austin, TX, USA
  1. Richard B. Stein, University of Alberta, 5005 Katz-Rexall Centre, Edmonton, Alberta, T6G 2E1, Canada. Email: richard.stein@ualberta.ca

Abstract

Background. Studies have demonstrated the efficacy of functional electrical stimulation in the management of foot drop after stroke. Objective. To compare changes in walking performance with the WalkAide (WA) foot-drop stimulator and a conventional ankle–foot orthosis (AFO). Methods. Individuals with stroke within the previous 12 months and residual foot drop were enrolled in a multicenter, randomized controlled, crossover trial. Subjects were assigned to 1 of 3 parallel arms for 12 weeks (6 weeks/device): arm 1 (WA–AFO), n = 38; arm 2 (AFO–WA), n = 31; arm 3 (AFO–AFO), n = 24. Primary outcomes were walking speed and Physiological Cost Index for the Figure-of-8 walking test. Secondary measures included 10-m walking speed and perceived safety during this test, general mobility, and device preference for arms 1 and 2 for continued use. Walking tests were performed with (On) and without a device (Off) at 0, 3, 6, 9, and 12 weeks. Results. Both WA and AFO had significant orthotic (On–Off difference), therapeutic (change over time when Off), and combined (change over time On vs baseline Off) effects on walking speed. An AFO also had a significant orthotic effect on Physiological Cost Index. The WA had a higher, but not significantly different therapeutic effect on speed than an AFO, whereas an AFO had a greater orthotic effect than the WA (significant at 12 weeks). Combined effects on speed after 6 weeks did not differ between devices. Users felt as safe with the WA as with an AFO, but significantly more users preferred the WA. Conclusions. Both devices produce equivalent functional gains.

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