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I HAVE PARKINSON'S DISEASES AND THOUGHT IT WOULD BE NICE TO HAVE A PLACE WHERE THE CONTENTS OF UPDATED NEWS IS FOUND IN ONE PLACE. THAT IS WHY I BEGAN THIS BLOG.

I COPY NEWS ARTICLES PERTAINING TO RESEARCH, NEWS AND INFORMATION FOR PARKINSON'S DISEASE, DEMENTIA, THE BRAIN, DEPRESSION AND PARKINSON'S WITH DYSTONIA. I ALSO POST ABOUT FUNDRAISING FOR PARKINSON'S DISEASE AND EVENTS. I TRY TO BE UP-TO-DATE AS POSSIBLE.

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I JUST WANT TO SHARE WITH YOU WHAT I READ ON THE INTERNET. IT IS UP TO YOU TO DECIDE WHETHER TO READ IT AND TALK IT OVER WITH YOUR DOCTOR. I AM JUST THE COPIER OF DOCUMENTS FROM THE COMPUTER. I DO NOT HAVE PROOF OF FACT OR FICTION OF THE ARTICLE. I ALSO TRY TO PLACE A LINK AT THE BOTTOM OF EACH ARTICLE TO SHOW WHERE I RECEIVED THE INFORMATION SO THAT YOU MAY WANT TO VISIT THEIR SITE.

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TRANSLATE

Thursday, April 3, 2014

Poor Is Top Reason Trials Don’t Make It to the Finish Line

FoxFeed Blog

Posted by  Maggie McGuire, March 24, 2014
Poor Recruitment Is Top Reason Trials Don’t Make It to the Finish Line
You’ve heard it time and time again: studies need you! You with Parkinson’s disease. You without Parkinson’s disease (PD)!
recent paper in The Journal of the American Medical Association backs us up. A long list of investigators looked at more than 1,000 clinical trials (not just PD ones) approved by six ethics committees spread across France, Switzerland and Canada. Of 1,017 studies, 253 were discontinued. That means almost a quarter of clinical trials from those sites never made it to analysis. Did the intervention work? Who knows.
The most cited reason for discontinuation was, unsurprisingly, poor participant recruitment. Practically 10 percent (9.9) of all the studies in this analysis (101/1,017) were stopped because they didn’t have enough volunteers. Trials need a certain number of patients — and oftentimes control volunteers — to have enough “power.” That is, the findings need to be significant enough to be generalized to the greater patient population.
What can you do? Register for Fox Trial Finder, which matches users to Parkinson’s studies they may be eligible for based on factors like location, age and medical history.
Want to know more? Read the article in JAMA.

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