Percutaneous Neuromodulation for Cervical Pain in University Students
This study aims to evaluate the effectiveness of percutaneous neuromodulation in increasing the pain threshold for university students experiencing cervical pain.
Ecoguided Percutaneous Neuromodulation
Neurologic Manifestations+2
+ Pain
+ Signs and Symptoms
Treatment Study
Summary
Study start date: August 31, 2024
Actual date on which the first participant was enrolled.The study aims to explore how Ecoguided Percutaneous Neuromodulation can help with neck pain in university students. Neck pain is a common issue, especially among students who spend a lot of time studying or using computers. This study focuses on students from San Pablo-CEU University, divided into two groups: those with neck pain and those without. This research is important because it seeks to find new ways to alleviate neck pain, which can significantly affect daily activities and quality of life. Participants in the study will undergo a procedure called Ecoguided Percutaneous Neuromodulation, which involves using a needle to stimulate nerves through the skin with the help of ultrasound guidance. The study will monitor any changes in neck pain levels in those who receive the treatment. The results will help understand if this method is effective in reducing neck pain and improving comfort and function for students suffering from this condition.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.52 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location