Prevalence and clinical correlates of apathy in Parkinson's disease: A community-based study

2009 ◽  
Vol 15 (4) ◽  
pp. 295-299 ◽  
Author(s):  
Kenn Freddy Pedersen ◽  
Jan Petter Larsen ◽  
Guido Alves ◽  
Dag Aarsland
2010 ◽  
Vol 25 (15) ◽  
pp. 2587-2594 ◽  
Author(s):  
Michael Y. Shino ◽  
Valerie McGuire ◽  
Stephen K. Van Den Eeden ◽  
Caroline M. Tanner ◽  
Rita Popat ◽  
...  

2018 ◽  
Vol 129 (8) ◽  
pp. e48-e50
Author(s):  
K.A. Schindlbeck ◽  
A. Vo ◽  
K. Fujita ◽  
P.J. Mattis ◽  
F. Marzinzik ◽  
...  

2011 ◽  
Vol 82 (10) ◽  
pp. 1112-1118 ◽  
Author(s):  
J. R. Evans ◽  
S. L. Mason ◽  
C. H. Williams-Gray ◽  
T. Foltynie ◽  
C. Brayne ◽  
...  

2020 ◽  
Vol 35 (8) ◽  
pp. 1287-1292 ◽  
Author(s):  
Roberto Cilia ◽  
Salvatore Bonvegna ◽  
Giulia Straccia ◽  
Nico Golfrè Andreasi ◽  
Antonio E. Elia ◽  
...  

2020 ◽  
Vol 7 (6) ◽  
pp. 1732-1739
Author(s):  
Susan G Klappa ◽  
Julie A I Thompson ◽  
Stuart Blatt

The purpose of this study was to investigate grit, exercise, and quality of life (QOL) among individuals diagnosed with Parkinson’s disease (PD). A sample of convenience was used. A survey which included the grit scale, QOL scale, and open-ended questions was distributed to participants (n = 101, 51 male and 50 female) who are members of online PD support groups across the United States. Data were analyzed by SPSS 25. Grit values averaged 3.65 ± 0.51 for participants (n = 101). When divided into groups, mean grit score for community-based exercisers was 3.78 ± 0.42 and 3.10 ± 0.48 for home-based exercisers. Grit was positively correlated to higher QOL on the Parkinson’s disease quality of life (PDQL; r = +0.293, P = .004). Grit was positively correlated to the emotional component of the PDQL ( r = +0.462, P < .001). Participants with higher grit levels had higher emotional coping responses after being diagnosed with PD, exercised more, and were more willing to self-advocate. With limited rehabilitation visits allowed, physical therapists should be aware of community-based programs to redefine participation roles after diagnosis.


2019 ◽  
Vol 398 ◽  
pp. 31-38 ◽  
Author(s):  
Heather Wilson ◽  
Flavia Niccolini ◽  
Clelia Pellicano ◽  
Marios Politis

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