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

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06480851
Enrollment
52
Registered
2024-06-28
Start date
2024-08-31
Completion date
2025-11-30
Last updated
2026-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neck Pain

Keywords

pain, Ecoguided Percutaneous Neuromodulation

Brief summary

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).

Interventions

PROCEDUREEcoguided Percutaneous Neuromodulation

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

Sponsors

CEU San Pablo University
Lead SponsorOTHER
Universidad Católica de Ávila
CollaboratorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Pain thresholdup to 1 WeekPortable hand pressure algometer (FPX 50/220, Wagner Instruments, Greenwich, USA), measured in kg / cm² (kilogram per centimeter squared).

Secondary

MeasureTime frameDescription
Pain by visual analog scaleBaselineusual visual analog scale (VAS) of pain (line from 0: no pain to 10:worst pain)
Neck Disability Index Questionnaire.BaselineQuantification of pain and disabilty
KinesiophobiaBaselineMeasured with Tampa Kinesiophobia Scale questionnaire (TSK-11SV) Spanish version. Minimum and maximum values are between 11 and 44 point, a result with higher values indicates higher level of kinesiofobia.
Pain Catastrophizing ScaleBaselinePain Catastrophizing Scale (PAS) will be used to evaluate the participants' pain-related thoughts and feelings.
Health-related quality of lifeBaselineThe Short Form Health Questionnaire (SF-36) questionnaire, which examines health-related quality of life under eight sub-titles; It consists of 36 items. The SF36 questionnaire will be used in the study.
SonoelastographyBaselineThis diagnostic test would be executed by a Physiotherapist who has experiences of using General Electric, P9 model ultrasound system for more than three year. The equipment to obtain the image will be used with a frequency of 12 MHz, 22 dB gain, 85 dynamic range, brightness at 17 and depth of 4 cm. The transducer will be placed on the spinosa of C4 and the probe will be moved towards the transverse of each of the sides, to identify the image of the multifidus muscle in depth. Once the muscle is located in this segment, a longitudinal and transverse image of the muscle will be obtained, performing the elastography at the same time and calculating the elastographic values (tissue resistance in kilopascals and transmission speed in meters/second).

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026