Cognitive factors associated with activity, participation in everyday life among people with MS

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Kessler Foundation researchers found that processing speed is the primary limiting factor associated with activity and participation in everyday life among people with multiple sclerosis (MS). "Factors that moderate activity limitation and participation restriction in people with multiple sclerosis" was published in the American Journal of Occupational Therapy (doi: 10.5014/ajot.2015.014332). This is the first MS study of cognition and measures of activity and participation. The authors are Yael Goverover, PhD, of New York University and visiting professor at Kessler Foundation, and Lauren Strober, PhD, Nancy Chiaravalloti, PhD, and John DeLuca, PhD, of Kessler Foundation.

MS, the leading cause of disability in working age adults, has a substantial negative impact on quality of life. The employment rate declines from 90% to 20% to 30% within five years of diagnosis, and only 35% of individuals with documented MS report normal social and lifestyle activities. Identifying modifiable factors associated with these limitations may help occupational therapists develop effective interventions. Because cognitive impairments are often implicated in declines in social participation and employment, researchers examined cognitive factors associated with both activity and participation. The study, which included 72 individuals with MS, focused on cooking ability for activity and employment status for participation. Assessment included neuropsychological testing of memory, executive function, visual perception, and processing speed, and questionnaires about fatigue, affective symptoms, activity and participation.

"The only variable significantly related to activity and participation was processing speed, "noted Dr. Goverover. "For occupational therapists, this means that implementing strategies that improve processing speed may help people with MS maintain their daily activities and stay in the workplace. In light of the close association between cognitive factors and cooking, providers should be aware that decline in cooking skills may be sign of cognitive decline in MS."

Comments

  1. Adriann Giovanni Adriann Giovanni United States says:

    Trying to understand all these studies and the money wasted .. Tell us , the patient something we do not already know .. Our Cognitive Skills are based on MANY factors .. One only needs to take a peek into the World of MS people ..

    By that I mean , we are all given the usual speech , that no two people are the same .. Yet somehow we are when it comes to Fatigue and Cognitive .. There are more than two people who talk of the same issues ..

    The Weather , the Daily routines , the trying to maintain the "Job" .. No matter what they are doing there is usually the decline , the pain , the Fatigue that brings on the loss of the thinking process ..

    We find times of the day we are better at , some people drink too much coffee and then "crash" , taking all forms of meds to keep the bloodflow going in hopes they can keep up with "normal" people .. But the Brain grows weary , the Eyes go and then the speech and body ..

    So , what was the point of this article ?? To us , it is for all you who are in search of "Grants" or "Research" money .. I say and many of the MS World , the People who live with it , we want the money .. To be able to afford the drugs & equipment that some require but cannot afford ..

    We want to sit on these Research Boards and choose who gets what and why .. We want a say !!  We are the ones who are the frontline while all these others TALK about MS including the NMSS here in the US , But we see and feel the daily grind .. Advocate for ourselves ..

    Yes !!! Not articles that say nothing ...

  2. Catherine Frost Catherine Frost France says:

    Oh yes Adriann, right on and it made enjoyable reading, thank you.
    We read (and hear) similar studies over here in France carried out by medical organisations and R&D groups after, as you say, grants and subventions.
    If I didn't have MS perhaps I'd read and say "Wow, fancy that!"!; instead I suffer from MS and say "But we all KNOW that; everybody has said time and time again. Please, what can be done to HELP us?" Surely we could put the money towards something practical; something useful..
    For goodness sakes please tell us something useful. Thank you!

The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
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