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Table 2 Inclusion and exclusion criteria

From: The efficacy of transcutaneous electrical nerve stimulation on the improvement of walking distance in patients with peripheral arterial disease with intermittent claudication: study protocol for a randomised controlled trial: the TENS-PAD study

Inclusion criteria

Unilateral Leriche-Fontaine stage-II PAD, admitted to a cardiovascular rehabilitation unit

Men or women

Aged 18 to 85 years

Able to take part in an outpatient rehabilitation programme

Clinically stable

Sedentary

Provided informed consent to participate in the study

Exclusion criteria

Age >85 years

Ward of court

Walking disorders related to orthopaedic or neuromuscular disease

Participation in a structured physical reconditioning programme in the month before the study

Renal insufficiency requiring dialysis

Known and documented myopathy

Progressive cancer

Associated progressive disease causing a deterioration in general health

Participation in another research protocol

Skin disorder making it impossible to use TENS

Absolute contraindication to physical activity

Presence of a pacemaker/defibrillator

  1. PAD peripheral arterial disease, TENS transcutaneous electrical nerve stimulation