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ANZSVS Conference 2026
The Foot-PAD Trial: A Double-Blind, Randomised Placebo-Controlled Trial of Footplate Neuromuscular Electrical Stimulation on Walking Capacity in Patients with PAD
Verbal Presentation

Verbal Presentation

8:49 am

10 September 2026

Peripheral Artery Disease

Disciplines

Vascular Surgery

Presentation Description

Institution: University of the Sunshine Coast - Queensland, Australia

Purpose: Patients with peripheral artery disease (PAD) experience leg muscle pain that limits walking and the ability to adhere to exercise therapy. Neuromuscular electrical stimulation (NMES) induces exercise-like muscle contractions and can be performed without pain. We hypothesised that a 12-week program of NMES would improve walking capacity compared with placebo-control in patients with PAD. Methodology: This was a single-centre, double-blind, randomised placebo-controlled trial. 180 patients with PAD (n=90 per group; mean age: 72 ± 9 y; ABI: 0.69 ± 0.20) were randomised to a 12-week program of NMES or sham placebo-control (CON). This was followed by a 6-week off-intervention follow-up. Outcomes were assessed at baseline (week 0), midway (week 6) and at the end of the intervention period (week 12), and again at the end of the follow-up phase (week 18). Participants used a footplate-NMES device (Revitive Medic Coach) for 2x30 min periods each day to deliver stimulation sufficient to induce contraction of the leg muscles. Control participants used a sham device that does not induce muscle contraction. Primary outcome was maximum distance during the six-minute walk test (6MWT). Secondary outcomes included pain-free distance during the 6MWT, and maximum and pain-free walking time during a graded treadmill test. Results: There was no difference in 6MWT distance between groups at week 12 (marginal mean difference (MMD): 3.68 m; 95% CI: -4.21 to 11.56; P = 0.361). At week 18, six weeks after the intervention ceased, 6MWT distance was greater in the NMES group compared with CON (MMD: 10.77 m; 95% CI: 2.82 to 18.72; P = 0.008). Pain-free 6MWT distance increased and was greater in the NMES group compared with CON at week 12 (MMD: 23.08 m; 95% CI: 6.55 to 39.61; P = 0.024). Conclusion: NMES may represent a valuable adjunct therapy to improve symptoms in patients with PAD.
Speakers
Authors
Authors

Prof Christopher Askew - , Dr Mark Windsor - , Dr Krist Feka - , Dr Meegan Walker - , Dr Mia Schaumberg - , A/Prof Fraser Russell - , Prof Bruce Neal - , Prof Adrian Esterman - , Mr Lucas Litewka - , Prof Mary Mcdermott - , Prof Jonathan Golledge - , A/Prof Pankaj Jha - , Dr Karl Schulze - , Dr Rebecca Magee - , Dr Jill O'Donnell - , Dr Jason Jenkins - , Ms Julie Jenkins - , Dr Vivienne Moult - , Dr Amanda Shepherd - , Dr Sarah Philpot - , Dr Daniel Mcglade - , The Footpad Trial Group -