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#1 | ||
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Member
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MJFF is working on a some projects related to clinical studies in PD and wonder if some of you might help us with nomenclature. We are interested in hearing feedback on community preferences on how to refer to PD clinical study participants.
For instance, MJFF is about to launch a clinical study that will involve newly diagnosed, unmedicated people with PD and healthy adults who are not first degree blood relatives of someone with PD. How best should we refer to these two audiences in presenting the study to the general public. We would welcome your feedback on whether you like these and/or new names we should consider. Looking at some of the suggested pairings below, is there is a clear consensus (pro or con). Or, how might you mix and match? Many thanks...Debi PD Patients and Healthy Volunteers PD Participants and Non-PD Participants PD Patient Volunteers and PD Community Volunteers PWP (People with Parkinson’s) and PD Partners |
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#2 | |||
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Senior Member
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Hi Debi - I like "PD participants and Non-PD participants"
thanks for asking!
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Carey “Cautious, careful people, always casting about to preserve their reputation and social standing, never can bring about a reform. Those who are really in earnest must be willing to be anything or nothing in the world’s estimation, and publicly and privately, in season and out, avow their sympathy with despised and persecuted ideas and their advocates, and bear the consequences.” — Susan B. Anthony |
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#3 | ||
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In Remembrance
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I also like pd and non-pd participants. It's easy to abbreviate as pd and non-pd and it doesn't make any comparisons about health.
thanks, paula
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paula "Time is not neutral for those who have pd or for those who will get it." |
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#4 | ||
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Member
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This is more cumbersome - but in my view, responsibly accurate:
People Diagnosed with PD and People Not Diagnosed with PD |
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#5 | |||
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Senior Member
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#6 | |||
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Senior Member
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Laura - the ironic beauty of this MJFF biomarker study is that it hopefully will go a long way in determining the accuracy of a PD dx and the range/definition of "Parkinsonian" disorders!
cheers! p.s. I love your picture; reminds me of an Indigo Girls song (why my name is "indigogo"): "Don't Give that Girl a Gun" !!!
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Carey “Cautious, careful people, always casting about to preserve their reputation and social standing, never can bring about a reform. Those who are really in earnest must be willing to be anything or nothing in the world’s estimation, and publicly and privately, in season and out, avow their sympathy with despised and persecuted ideas and their advocates, and bear the consequences.” — Susan B. Anthony Last edited by indigogo; 04-28-2010 at 11:02 AM. Reason: add ps |
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#7 | |||
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Senior Member
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agree with fiona & laura
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Jean B This isn't the life I wished for, but it is the life I have. So I'm doing my best. |
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"Thanks for this!" says: | anon72219 (04-29-2010) |
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#8 | |||
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Senior Member
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These terms will be used when reaching out to those newly diagnosed with PD. Will they understand "control group?" I think "control" would be problematic.
Regardless of how we feel personally about the terms, in the end, what descriptive words and/or phrases will be most clear to the target group?
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Jean B This isn't the life I wished for, but it is the life I have. So I'm doing my best. |
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#9 | |||
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Member
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people with pd and people without pd
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I have a post-encephalitic neurological disorder, but it does NOT have me! |
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#10 | ||
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In Remembrance
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for symplicity, is the nonpd control participant redundant?
another suggestion:just assume pd is understood. you could just go with: patient participant and control participant= patients vs.controls or pd patient and control partcipant = patients vs.control I would think that whatever you do it will become abbreviated to patients vs. controls in everyday usage.
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paula "Time is not neutral for those who have pd or for those who will get it." |
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