Neuromuscular Electrical Stimulation in Foot and Ankle Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorNYU Langone Health

About this trial

This is a pilot randomized controlled trial, wherein the intervention group will undergo NMES five days a week beginning three weeks postoperative and lasting for ten weeks. Both the control and intervention groups will start standard physical therapy six weeks postoperative. Primary outcome measure will be the isometric strength of the gastrocnemius muscle. The secondary outcomes will comprise subjective clinical evaluations (using the Lower Extremity Functional Scale \[LEFS\]), functional assessments such as the sit-to-stand test, 2-minute walk test, stair climb test and objective clinical evaluation using contralateral comparison of calf circumference.

Eligibility criteria

Qualifiers

Capable and willing to provide informed consent

Undergoing a procedure that involves repairing an ankle fracture.

Disqualifiers

Rheumatoid arthritis

Connective tissue disorders

Chronic corticosteroid use

Implanted electrical devices

Trial design

Treatments tested in this trial

  • VPOD Wireless Tens Unit
  • Physical Therapy
  • Biodex

Treatment groups

20 Participants
are divided into 2 treatment groups

Sponsors and collaborators