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Dermatome Electrical Stimulation on Individuals With Overweight and Class I Obesity

Obesity Clinical Trial

Official title:
Effect of T6 Dermatome Electrical Stimulation on Gastric Motor Functions, Appetite, Satiation, Satiety and Weight Loss in Individuals With Overweight and Class I Obesity

Clinical Trial Summary

Investigators are doing this research study to find out the effect of T6 dermatomal electrical stimulation (delivered by a Transcutaneous Electrical Nerve Stimulation (TENS) unit) on appetite and weight loss.

Clinical Trial Description

Participants will be treated before and after two meals of the day with T6 dermatomal electrical stimulation delivered by a Transcutaneous Electrical Nerve Stimulation (TENS) unit. Participants will receive 15-minute T6 dermatome cutaneous stimulation with TENS unit applied immediately before ingestion of two of main meals of the day (breakfast and evening meal), and 60 minute stimulation applied immediately after ingestion of these meals. Participants will apply the stimulus four times daily for a treatment period of at least 3 months. Participants will keep a diary of weight once weekly and a weekly appetite record. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03261531
Study type Interventional
Source Mayo Clinic
Contact
Status Terminated
Phase N/A
Start date February 21, 2017
Completion date January 30, 2019
View Details
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