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Effectiveness of Percutaneous Neuromodulation in the Treatment of Cervical Pain in University Students.

NCT ID: NCT06480851

Last Updated: 2024-06-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

52 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-08-31

Study Completion Date

2024-11-30

Brief Summary

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A non-randomized experimental study will be conducted to investigate the effect of Ecoguided Percutaneous Neuromodulation on patients with and without neck pain in college students. The sample will be collected in a non-probabilistic way at convenience among the students at the San Pablo-CEU University, with a sample that will be divided into two groups: group 1 (G1) with neck pain and group 2 (G2).

Detailed Description

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Conditions

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Neck Pain

Keywords

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pain Ecoguided Percutaneous Neuromodulation

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Neck Pain Group

Group Type EXPERIMENTAL

Ecoguided Percutaneous Neuromodulation

Intervention Type PROCEDURE

Ecoguided Percutaneous Neuromodulation over the posterior branch of the cervical multifidus, for 10 minutes, with a frequency of 10 HZ.

Non Neck Pain Group

Group Type ACTIVE_COMPARATOR

Ecoguided Percutaneous Neuromodulation

Intervention Type PROCEDURE

Ecoguided Percutaneous Neuromodulation over the posterior branch of the cervical multifidus, for 10 minutes, with a frequency of 10 HZ.

Interventions

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Ecoguided Percutaneous Neuromodulation

Ecoguided Percutaneous Neuromodulation over the posterior branch of the cervical multifidus, for 10 minutes, with a frequency of 10 HZ.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Current Cervical Pain on a Visual Analog Scale (VAS) greater than 3.
* Neck pain in the last 12 weeks, and no treatment has been performed.
* Disability index of 8% or more on the Neck Disability Index.
* That they have undergone treatment.

Exclusion Criteria

* Neck pain associated with vertigo.
* Osteoporosis (control X-ray).
* Diagnosed psychological disorders.
* Vertebral fractures (control X-ray).
* Tumors.
* Diagnosed metabolic diseases.
* Neck surgery.
* Belonephobia.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Universidad Católica de Ávila

OTHER

Sponsor Role collaborator

CEU San Pablo University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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San Pablo CEU University

Boadilla del Monte, Madrid, Spain

Site Status

Countries

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Spain

Facility Contacts

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Francisco García-Muro San José, MSc, PT

Role: primary

Other Identifiers

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CEU-026

Identifier Type: -

Identifier Source: org_study_id