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NCT05487131 Clinical Trial

Neuromodulation and Fatigue

Fatigue Clinical Trial

Official title:
Neuromodulation and Fatigue

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05487131
Other study ID # 14921
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 3, 2023
Est. completion date December 29, 2024

Study information
Verified date November 2023
Source University of Oklahoma
Contact Hugo Pereira, PhD
Phone 405-325-2773
Email hugomax@ou.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this project, we aim to determine any potential effects of a weak electrical current applied to the neck or thoracic area on functional capacity and muscle activation. Healthy individuals will participate in one familiarization followed by three experimental sessions. Fatigability and motor function will be assessed in each test session.

Recruitment information / eligibility
Status Recruiting
Enrollment 40
Est. completion date December 29, 2024
Est. primary completion date September 29, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: Healthy individuals between 18 and 50 years old Exclusion Criteria: Metal implants or joint replacement. Presence of neuromuscular disease. Skin hypersensitivity.

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• electrical stimulation
different types of weak electrical stimulation will be used

Locations
Country Name City State
United States University of Oklahoma Norman Oklahoma

Sponsors (1)
Lead Sponsor Collaborator
University of Oklahoma

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Force Change in force will be evaluated with a device during each test session Each session will take approximately 2 hours (total of 4 test sessions)
Primary Perception of effort Change in perceived effort will be evaluated with visual analogue scales Each session will take approximately 2 hours (total of 4 test sessions)
Primary Muscle activation Electromyography will be used to quantify muscle activation Each session will take approximately 2 hours (total of 4 test sessions)
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