Vertical current steering (vCS) divides current between multiple contacts, which reduces radial spread to fine-tune the electric field shape and improves neuroanatomical targeting. vCS may improve the variable responsiveness of Parkinsonian gait to conventional deep brain stimulation. We hypothesized that vCS elicits greater improvement in ambulation in Parkinson's disease patients compared to conventional, single-contact stimulation. vCS was implemented with divisions of 70%/30% and 50%/50% and compared to single-contact stimulation with four therapeutic window amplitudes in current-controlled systems. Walking at a self-selected pace was evaluated in seven levodopa-responsive patients. Integrative measures of gait and stimulation parameters were assessed with the functional ambulation performance (FAP) score and total electrical energy delivered (TEED), respectively. A twotailed Wilcoxon matched-pairs signed rank test assessed the effect of each stimulation condition on FAP and TEED and compared regression slopes; further, a two-tailed Spearman test identified correlations. vCS significantly lowered the TEED (P < 0.0001); however, FAP scores were not different between conditions (P = 0.786). Compared to single-contact stimulation, vCS elicited higher FAP scores with lower TEED (P = 0.031). FAP and TEED were positively correlated in vCS (P = 2.000 × 10-5 , r = 0.397) and single-contact stimulation (P = 0.034, r = 0.205). Therefore, vCS and single-contact stimulation improved ambulation similarly but vCS reduced the TEED and side-effects at higher amplitudes. Parkinson's disease and deep brain stimulation Deep brain stimulation (DBS) consistently relieves appendicular symptoms in Parkinson's disease (PD) but its effect on Parkinsonian gait deficits remains more elusive and variable 1. Thus, in present clinical practice, PD patients with severe postural and gait instabilities or levodopa (L-DOPA) resistant postural and gait instabilities are often excluded from receiving DBS 2-4. DBS chronically transmits electrical pulses from a sub-dermally implanted impulse generator (IPG) in the upper chest to neural tissue through implanted electrodes to address disabling dyskinesia and motor fluctuations from long-term use of L-DOPA 5. The varying response of Parkinsonian gait deficits to DBS may be attributed to extensive physiological integration of various networks necessary for gait facilitation, the influence of bradykinesia and rigidity on Parkinsonian gait deficits, and the bias of upper limb symptom improvement during contact localization and selection 6,7. Gait deficits attributed to rigidity and bradykinesia such as reduced step length and gait velocity tend to respond to L-DOPA and subthalamic nucleus (STN)-DBS. However, L-DOPA responsive gait deficits still exhibit a more variable responsiveness to STN-DBS as compared to appendicular symptoms such as tremor and rigidity. For instance, stimulation spread into the zona incerta and/or fields of forel from STN targeted electrodes has been reported to induce gait akine...