Please be patient, I’ll be with you shortly: elucidating experiences and strategies in freezing of gait in Parkinson’s Disease
Jade Park1, Jessica Hemm2, Bichun Ouyang1, Jori Fleisher2
1Rush University Dept. of Neurological Sciences, 2Rush University Parkinson's and Movement Disorders Program
Objective:
To compare experiences and compensatory strategies in freezing of gait (FoG) between individuals with Parkinson’s Disease (PD) plus cognitive impairment (PD+CI) versus PD alone. 
Background:
PD patients with CI, even mild cognitive impairment (MCI), are often excluded from FoG studies, limiting our understanding of the scope of this phenomenon. 
Design/Methods:
In this prospective, single-center, mixed-methods study, we included participants with PD>3 years, MDS-UPDRS subjective and or objective FoG score(s)>2 (mild or worse), and Mini-Cog>0. PD+CI group was defined by Montreal Cognitive Assessment (MoCA)<26. Participants completed the MoCA and a ten-question semi-structured interview regarding FoG impact on daily life and coping strategies. Interviews were manually coded and analyzed using grounded theory for common themes.  
Results:
Eighteen participants comprised each PD+CI and PD group. The median MoCA for the PD+CI group was 21.5 vs. PD 27.5, p<0.0001. PD+CI participants commonly described FoG as a mind-body disconnect with loss of command over their body (27.8%), whereas the PD group often characterized FoG in physical terms as feet stuck or glued to the floor (33.3%). Approaches to overcome FoG unique to the PD+CI group were reactivating one’s attention (11.1%) and incorporating relaxation (11.1%), whereas those distinct to the PD group included visual cues (16.7%) and integrating morning exercise (11.1%). Both groups expressed that FoG was poorly understood by the public. The PD group held unique views in perceiving FoG as a physical liability to others and analogized public misinterpretation of FoG to intoxication. The PD+CI group disclosed and educated others about FoG more than the PD group.
Conclusions:
Both groups viewed public understanding of FoG as limited which discouraged participation in social activities. Educational initiatives around FoG as a part of the constellation of PD symptoms as well as venue arrangements, such as expedited entry and exit for those with FoG, may improve awareness and engagement.    
10.1212/WNL.0000000000209022
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