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Effects of Transcutaneous Neuromodulation and Cervical Exercise in Students With Chronic Nonspecific Cervical Pain

Not yet recruitingNot applicableNCT07452237
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

This randomized controlled trial aims to compare the effectiveness of a cervical exercise program, transcutaneous neuromodulation of the spinal accessory nerve, and a placebo intervention on pain intensity, pressure pain threshold, cervical proprioception, functional disability, depression, anxiety, and stress in university students with chronic non-specific neck pain. The study will include a six-week intervention period with pre- and post-treatment assessments. The findings may contribute to the development of accessible physiotherapy interventions within university settings.

Study details

Official title
Effects of Transcutaneous Neuromodulation and Cervical Exercise in Students With Chronic Nonspecific Cervical Pain
Interventions
  • Other: Supervised Cervical Exercise Program
  • Device: Low-Frequency Transcutaneous Neuromodulation
  • Device: Sham Transcutaneous Neuromodulation
Sponsor
Universidad Francisco de Vitoria
Start date
2026-04-01
Primary completion
2026-05-13
Sex
All
Age range
from 18 Years to 30 Years
Results posted
No results posted in this snapshot
Total sites listed
0

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * University students aged 18-30 years * Chronic non-specific neck pain lasting ≥ 3 months * Pain intensity \>3/10 on VAS * No pharmacological or physiotherapy treatment in the past 3 months Exclusion Criteria: * Specific cervical pathology (e.g., radiculopathy) * Neurological, cardiovascular, systemic, or infectious disease * Diagnosed psychological disorders * Pregnancy or postpartum period \< 1 year * Regular use of analgesics, opioids, or antidepressants * Previous cervical spine or shoulder surgery * Electronic implants * Neck pain associated with vertigo

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07452237