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RECRUITING
NCT06722391
NA

Neuromuscular Electrical Stimulation: A Novel Treatment for Improving Metabolism

Sponsor: University of Texas, El Paso

View on ClinicalTrials.gov

Summary

Once written consent is obtained, the participant will be provided with an accelerometer to be worn for 7 days to assess current physical activity levels. Subjects will be provided with a standardized diet (55/15/30% CHO/PRO/FAT) prior to collection of pre-intervention data of insulin sensitivity. Individuals will then participate in an 8-week electrical stimulation intervention (30min/day, 3x/week) and randomized into placebo/control, NMES, resistance training combined with NMES (RT +NMES), or resistance training (RT) group (n=20 per group), followed by collection of post-intervention data. The control group will receive electrical stimulation up to sensory level, the NMES group will receive stimulation up to tolerable intensity to induce visible muscle contraction, the RT+ NMES will receive stimulation up to tolerable intensity during resistance training, and the RT group will only receive exercise training. Control and NMES group will self administer stimulation at home. Pre-and post-intervention data includes measurements for body composition, resting metabolic rate, VO2max, insulin sensitivity, and comprehensive blood work.

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2024-08-19

Completion Date

2031-09-01

Last Updated

2024-12-09

Healthy Volunteers

Yes

Interventions

DEVICE

Neuromuscular Electrical Stimulation (Sensory)

Group will receive Electrical Stimulation up to sensory level

DEVICE

Neuromuscular Electrical Stimulation

Group will receive Electrical Stimulation up to maximum tolerable level

OTHER

Resistance Training

Group will receive exercise training.

Locations (1)

University of Texas at El Paso

El Paso, Texas, United States