Hand Lateralization by Using EEG Analysis Method in Amputees

Status Completed

Clinical Trial Summary

Studies on the improvement of body image or body perception have proven their effectiveness in different clinical situations such as pain management and chronic pain treatment. The aim of this study is to evaluate the hand lateralization cognitive task by recording Electroencephalography (EEG) signals from different personal perspectives in amputees. In this study, the paradigm in which personal perspectives are evaluated over the hand lateralization task will be applied to amputees and healthy volunteer participants. Data will be recorded via EEG and Eprime software program.

Clinical Trial Description

The aim of this study is to evaluate the hand lateralization cognitive task by recording Electroencephalography (EEG) signals from different personal perspectives in amputees. In this study, the paradigm in which personal perspectives are evaluated over the hand lateralization task will be applied to amputees and healthy volunteer participants. It was planned to enroll two groups to the study. One group is named "amputees" the other one is "control". Control group will be matched in terms of age and gender with the amputees group. Before hand lateralization test, participants will be evaluated regarding eligible criterias and EEG paradigm regarding hand lateralization will be performed for each participant. Both groups (Amputees and Control) will complete "hand lateralization program" for at least 10 days. The test will be sent each day on an online system. Participants' performances will be recorded via online system. Following 10-day period, EEG paradigm regarding hand lateralization will be performed for each participant, again. Before and after comparisons will be analyzed. Data will be recorded via EEG and Eprime software program. EEG-Event Related Oscillation (power spectrum, phase locking) analysis will be performed for each frequency bands: alpha, theta, beta, gamma. Eprime analysis will be performed for the data of reaction time and accuracy rate. ;

Study Design

Related Conditions & MeSH terms

Body Image

Clinical Trial Details

NCT number	NCT05339776
Study type	Interventional
Source	Trakya University
Contact
Status	Completed
Phase	N/A
Start date	March 1, 2021
Completion date	March 27, 2023

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