Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07161648

Use of Neuromuscular Electrical Stimulation to Prevent Exercise Resistance

The study will find out if 100 minutes of electrical stimulation of muscle prevents the unfavorable consequence of insufficient exercise.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Exercise resistance is characterized by the absence of exercise induced improvements in fat metabolism following a meal, and results from prolonged sedentary behavior between successive workouts (i.e. 2+ sedentary days between exercise bouts). The suggested energy expenditure threshold for avoiding exercise resistance is the equivalent of walking ~8,500 steps/day. However, population data indicate that the typical adult in the US only walks 5,000 steps/day (i.e. 3,500 steps below the threshold). Neuromuscular Electrical Stimulation (NMES) evokes skeletal muscle contractions and increases energy expenditure. The hypothesis to be explored in this current proposal is: NMES will prevent exercise resistance. The plan is to induce exercise resistance via short-term abstention from activity other than exercise, and then on a separate occasion, use NMES to prevent exercise resistance (i.e. the short-term abstention from exercise will be "replaced" with NMES).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Regularly active (more than 30 minutes of exercise per day, 3 days per week, over the previous 12 months)
  • Ability to complete at least one hour of treadmill exercise (i.e. jogging/running),
  • Willing to abstain from caffeine and alcohol for 24-hours prior to three different study visits
  • Competency in English

Exclusion criteria

  • Current or previous injuries that may hinder a participant's ability to exercise on a treadmill
  • A history of cardiopulmonary disorder that may be contra-indicative to treadmill exercise
  • Current use of cardio-pulmonary medication to treat a cardio-pulmonary condition
  • Currently breastfeeding
  • Pregnancy

Treatment and study plan

Neuromuscular electrical stimulation

Other

The study participants will engage in 100-minutes of neuromuscular electrical stimulation (NMES). NMES pads are sticky pieces of plastic, similar in size to a 25-cent coin. The pads will be placed on the bellies of thigh muscles (the vastus lateralis, vastus medialis), and calf muscles (the long and short head of the gastrocnemius). These skeletal muscles are selected due to their size (thereby promoting a bigger increase for metabolic rate compared with a small muscle), because they are relatively superficial, and because previous published studies of NMES used these anatomical locations.

Primary outcomes

  1. Fat oxidation

    Time frame: Blood will be sampled and triglyceride concentration measured. Study participants will eat a meal. Blood will be sampled and triglyceride concentration measured every 30-minutes for 4 hours.

    Circulating triglyceride concentration after eating a high fat meal.

Study contacts

Contact information is provided by the study sponsor or research team.

Ally Tripure, B.S.

CONTACT

[email protected]

9704913495

Christopher Bell, PhD

CONTACT

[email protected]

970-491-7522

Sponsors and collaborators

Lead sponsor

Colorado State University

Other

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Sep 8, 2025
Registry last updated
Nov 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.