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

Study acronym: TN-E-CNCP
StatusNot Yet Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated March 9, 2026 (before its estimated May 13, 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Study Identification, Study Status, Sponsor/Collaboratorsv2
  2. Study First Submitted
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.
Trial Details
NCT Number NCT07452237
Lead Sponsor Universidad Francisco de Vitoria
Conditions
(from sponsor)		 Chronic Non-specific Neck Pain
Related terms Neck Pain
Enrollment 51 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov