Ignite Creation Date:
2024-10-25 @ 8:02 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06544850
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-08-05
Brief Title:
Lateralization Performance in Chronic Low Back Pain
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Lateralization Performance and Two-point Discrimination in Patients With Chronic Low Back Pain A Cross-sectional Study
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The aim of our study was to examine the relationship between lateralization performance two-point discrimination kinesiophobia and pain catastrophizing in patients with chronic low back pain
Detailed Description:
Participants who meet the inclusion criteria and agree to participate in the study will be selected from the relevant population by the improbable random sampling method Demographic data age gender height weight education status and dominant hand and foot information will be obtained from the volunteer participants participating in the study before starting the study Oswestry Low Back Pain Questionnaire will be used to evaluate functional limitations in daily life activities of patients experiencing low back pain This questionnaire has 6 sections with 0-5 points for each question It consists of 10 sections including pain intensity personal precautions lifting objects walking sitting standing sleeping sexual life social life and travel 0-4 points are considered as no disability 5-14 points as mild 15-24 points as moderate 25-34 points as severe and 35-50 points as complete disability The minimum score received from the scale is 0 and the maximum score is 50 A score of 50 indicates the highest level of functional disability Recognize mobile application will be used to evaluate lateralization performance This application will be evaluated with the hand foot and back modules The photographs will be shown on a screen If the patient thinks the photo belongs to the right side the patient will press the right button and if the patient thinks the photo belongs to the left side the patient will press the left button The reaction time and accuracy given at the end of the application will be recorded The most accurate response instruction will be given in the shortest possible time The Visual Analog Scale VAS will be used to measure the general pain status of the patients In addition the duration of the pain the localization of the pain right left and the Tampa Kinesiophobia Scale will be used to evaluate the fear of movement This scale consists of 17 items A high score indicates a high level of fear of movement while a low score indicates a negligible level of fear of movement Each item is scored on a 4-point Likert scale 1-4 The answers and their numerical values are as follows 1 I strongly disagree 2 I disagree 3 I agree and 4 I strongly agree The scores of items 4 8 12 and 16 should be reversed when calculating the total score The total score obtained by adding different items can vary between 17-68 The level of pain catastrophizing will be assessed with the Pain Catastrophizing Scale This scale is a 5-point Likert-type scale consisting of 13 questions and evaluates the feelings and thoughts of the person when experiencing pain A two-point discrimination device will be used to assess two-point discrimination The Central Sensitization Inventory will be used for central sensitization findings Part A consisting of 25 items scored from 0 to 4 will be used A higher score indicates the presence of more symptoms related to central sensitization A cut-off value equal to or above 40 indicates the presence of central sensitization
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None