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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04130581
Other study ID # PSA1775
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 14, 2018
Est. completion date January 31, 2020

Study information

Verified date February 2020
Source Lancaster University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The research project explores how non-invasive brain stimulation can be used to detect and ameliorate loss of muscle strength after inactivity. At present, there is a limited understanding of how to maintain muscle strength during inactivity. Increasing evidence indicates that reduction in muscle strength following immobilisation is associated with reduced cortical motor output. Therefore, the aim of the study is to test if brain stimulation, can maintain cortical motor output and ameliorate the loss of muscle strength following immobilisation.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date January 31, 2020
Est. primary completion date January 31, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- Male

- right-handed

- aged 18-30

- healthy BMI

Exclusion Criteria:

- no primary muscle disorders

- no open wounds or skin conditions to arms and hands

- no neurological disorders or history of

- no history of fainting/convulsions

- no metal implanted into head/eye/neck

- non-smoker

- no arm, hand, fingers, shoulder injuries

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Transcranial Magnetic Stimulation (TMS)
TMS is a safe and non-invasive technique, which involves the generation of brief magnetic pulses applied to the head through a coil. The magnetic pulses pass through the scalp and skull and induce weak electric currents in the neural tissue directly underneath the coil. When TMS is applied in repetitive, patterned trains of pulses (rTMS), it can induce cortical plasticity specifically in the targeted brain region.

Locations

Country Name City State
United Kingdom Lancaster University Lancaster Lancashire

Sponsors (1)

Lead Sponsor Collaborator
Lancaster University

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Motor Evoked Potentials (MEPs) across time points MEPs are elicited via TMS to primary motor cortex and index the excitability of the motor pathway. They are recorded non-invasively from muscles using surface electrodes. At each time point of the study (0, 24, 48, 72 hours) record MEPs will be recorded pre and post-intervention from the hand muscles of the dominant (immobilised) arm, and non-dominant (non-immobilised arm), to evaluate changes in excitability. Specifically, the peak-to-peak value of the MEPs from the hand will be measured, which reflects the amplitude of the MEP response. The latency of the MEP to index neural conduction speed will also be measured. 0, 24, 48, and 72 hours
Secondary Change in grip strength across time points Grip strength of the dominant and non-dominant hands will be assessed using an isokinetic dynamometer at 0 and 72 hrs post-immobilisation. This will measure the strength of the hand muscles. 0, and 72 hours.
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