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.

Thursday, August 28, 2025

Post stroke Cardiorespiratory Exercise for Brain Volume and Cognition A Randomized Clinical Trial

Didn't all this earlier research already prove the point?

  • aerobic exercise (65 posts to February 2016)
  •  Post stroke Cardiorespiratory Exercise for Brain Volume and Cognition A Randomized Clinical Trial

     AmyBrodtmann,PhD;LeonidChurilov,PhD;KimberleyAdkins,MExPhys;RuwaydaHaibe,BMed-Hns;StephanieTucker,MExPhys;MohamedSalahKhlif,PhD; EmilioWerden,PhD;LauraJ.E.McCambridge,MSc;RachaelTelfer,MExPhys;SharonKramer,PhD;BarbaraR.Cardoso,PhD;MatthewPase,PhD; NathalieLaunder,BSc;NataliaEgorova-Brumley,PhD;StanleyHughwaHung,PhD;LouiseM.Burrell,MD;GavinWilliams,PhD;VincentThijs,PhD; JulieBernhardt,PhD;LiamJohnson,PhD;KathrynS.Hayward,PhD;PISCES-ZODIACInvestigators

    Abstract 


     IMPORTANCE Stroke increases the risk of cognitive impairment and dementia without proven prevention therapies. Cardiorespiratory exercise(CRX) preserves brain health. 
     OBJECTIVE

    To determine whether a CRX intervention preserves hippocampal volume(HV) and cognition in patients after ischemic stroke. DESIGN,SETTING,ANDPARTICIPANTSThePost-IschemicStrokeCardiovascularExerciseStudy (PISCES)–Zoom Delivered Intervention Against Cognitive Decline(ZODIAC) is a phase 2b assessor blinded randomized clinical trial performed at 4 metropolitan healthcare services in Melbourne, Australia. Eligible participants included adult patients who survived ischemic stroke without comorbidities prohibiting exercise or diagnosed cognitive disorder.(So cherry picking patients; violating the 'leave no survivor behind' idea! What if you're one of those patients? You'll want 100% recovery also. Better get cracking on that research NOW!) Participants were recruited from May26,2016, to March20,2020, forPISCES in-person training and from November9,2020, to February12,2024, for ZODIAC remotely delivered home training. A total of 6921 participants were screened for eligibility, 130 were recruited, 107 were randomized (34 in PISCES and 73 in ZODIAC), and 104 continued to intervention. Study visits at 2,4, and 12 months poststroke included brain magnetic resonance imaging and cognitive testing. Participants were randomized (1:1), stratified by baseline function (modified Rankin Scale score of 0-1 vs 2-3) and total brain volume. Primary, secondary efficacy, and safety outcome analyses were conducted using modified intention-to-treat (mITT) principle and per protocol. 
     INTERVENTION

    Participants received 8 weeks of three 60-minute sessions/wk. Participants in the CRX group received prescribed intensity progressive aerobic and resistance training; the control group received balance and stretching training. 
     MAIN OUTCOMES AND MEASURES 

    The primary outcome was relative change in HV calculated as the difference between HV at times 1and 2 divided by HV at time 1.Secondary outcome consisted of 12-month executive function test results (Trial Making Test, PartB[TMT-B]), adjusted for baseline TMT-Band mRS score. 
     RESULTS

    The104participants included in primary outcome mITT analysis(55 in the control and 49 in the CRX groups; mean[SD]age,64[14] years;67[64.4%] male; equivalent baseline mRS score). One hundred participants (33 in PISCES and 67 in ZODIAC) completed 4-month assessments, and 97 (31 in PISCES and 66 in ZODIAC) completed 12-month assessments. There were no intervention related serious adverse events. Mean (SD) difference in relative change in HV between the CRX (−0.26%[2.12%]) and control (−0.11%[2.35%]) groups was−0.10% (95%CI, −1.10%to0.87%; P =.83).  The CRX group (n = 43) performed better than the control group (n = 51) on the adjusted TMT-Bat 12 months (adjusted mean difference, −3.75[95%CI, −5.02to−2.49] seconds). 
     CONCLUSIONS AND RELEVANCE 

    In this randomized clinical trial of fitness training, CRX was safe but did not preserve HV more than a control condition. CRX may benefit cognitive preservation following ischemic stroke. TRIALREGISTRATION anzcrt.orgIdentifier:ACTRN12616000942459 JAMANetworkOpen.2025;8(8):e2528907.doi:10.1001/jamanetworkopen.2025.2890

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