Viewing Study NCT06468514



Ignite Creation Date: 2024-07-17 @ 11:00 AM
Last Modification Date: 2024-10-26 @ 3:32 PM
Study NCT ID: NCT06468514
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-06-25
First Post: 2024-06-15

Brief Title: Effectiveness of Neurodinamic Techniques on Radial Nerve for the Treatment of Lateral Epicondylalgia
Sponsor: University of Alcala
Organization: University of Alcala

Study Overview

Official Title: Effectiveness of Tensioning Techniques vs Sliding Techniques on Radial Nerve for the Treatment of Lateral Epicondylalgia
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: TT-ST-RN-LE
Brief Summary: Lateral elbow pain is a prevalent musculoskeletal disorder in the working population due to overuse of the upper limb This pathology has serious consequences for health work performance and overall health burden

In this injury as in any musculoskeletal disorder the peripheral nervous system is involved Because of its course and corresponding motor and sensory innervation in the area the radial nerve should be taken into consideration as a structure involved in elbow pain

The aim of the present study is to demonstrate which of the neurodynamic techniques is more effective in lateral epicondylalgia neural tension techniques or neural mobilization techniques
Detailed Description: The aim of the present study is to demonstrate which is more effective among the neurodynamic techniques for lateral epicondylalgia neural tension techniques or neural mobilization techniques

A total of 60 subjects will be recruited and divided into 2 groups 30 in Group 1 where they will receive a neural mobilization technique on the radial nerve and 30 in Group 2 where they will be subjected to a neural tension technique on the radial nerve

The data to be collected will be grip strength pain on pressure pain and quality of life dash questionnaire these data will be measured pre post treatment and a re-evaluation at 4 weeks and 24 weeks after the intervention

The duration of the treatment is 6 weeks performing two sessions per week with 72 hours of rest between sessions A total of 12 sessions will be carried out

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None