Effectiveness of Percutaneous Neuromodulation in the Treatment of Cervical Pain in University Students.
1 other identifier
interventional
52
1 country
1
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).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Aug 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 3, 2024
CompletedFirst Posted
Study publicly available on registry
June 28, 2024
CompletedStudy Start
First participant enrolled
August 31, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
November 30, 2025
CompletedJanuary 28, 2026
January 1, 2026
1.1 years
February 3, 2024
January 27, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pain threshold
Portable hand pressure algometer (FPX 50/220, Wagner Instruments, Greenwich, USA), measured in kg / cm² (kilogram per centimeter squared).
up to 1 Week
Secondary Outcomes (18)
Pain by visual analog scale
Baseline
Pain by visual analog scale
after intervention
Pain by visual analog scale
Follow-up at 1 week
Neck Disability Index Questionnaire.
Baseline
Neck Disability Index Questionnaire.
after intervention
- +13 more secondary outcomes
Study Arms (2)
Neck Pain Group
EXPERIMENTALNon Neck Pain Group
ACTIVE COMPARATORInterventions
Ecoguided Percutaneous Neuromodulation over the posterior branch of the cervical multifidus, for 10 minutes, with a frequency of 10 HZ.
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- Neck pain associated with vertigo.
- Osteoporosis (control X-ray).
- Diagnosed psychological disorders.
- Vertebral fractures (control X-ray).
- Tumors.
- Diagnosed metabolic diseases.
- Neck surgery.
- Belonephobia.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- CEU San Pablo Universitylead
- Universidad Católica de Ávilacollaborator
Study Sites (1)
San Pablo CEU University
Boadilla del Monte, Madrid, 28668, Spain
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 3, 2024
First Posted
June 28, 2024
Study Start
August 31, 2024
Primary Completion
September 30, 2025
Study Completion
November 30, 2025
Last Updated
January 28, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share