“…This added stressor multiplies the complexity of living with PD and has been found to have a significant detrimental effect on people's quality of life (Phu et al, 2014). Although ICDs are commonly under reported (Vilas, Pont-Sunyer, & Tolosa, 2011), it is estimated that between 10 and 14% of people with PD have ICDs (Giladi et al, 2007;Poletti et al, 2013;Weintraub, Potenza, Siderowf, & Voon, 2010), compared to between 1 and 8% within the general population (Dell'Osso, Altamura, Allen, Marazziti, & Hollander, 2006). Where explicit comparisons have been made between people with PD and matched controls, ICDs are around twice as common in Parkinson's patients than in controls (Rodriguez-Violante, Gonzalez-Latapi, Cervantes-Arriaga, Camacho-Ordonez, & Weintraub, 2015), although the difference can be even greater (Perez-Lloret, Rey, Fabre, Ory, Spampinato, Brefel-Courbon, Montastruc, & Rascol, 2012).…”