[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100627715":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":28,"centralContacts":28,"locations":28,"responsibleParty":34,"collaborators":28,"id":38,"slug":39,"hasResults":40,"nctId":41,"briefTitle":42,"officialTitle":42,"acronym":43,"eligibilityCriteria":44,"healthyVolunteers":40,"sex":45,"minAge":46,"maxAge":47,"enrollmentInfo":48,"targetDuration":28,"studyType":51,"phases":52,"briefSummary":54,"conditions":55,"keywords":57,"overallStatus":65,"whyStopped":28,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":28},{"fullName":5,"class":6},"Universidad Francisco de Vitoria","OTHER",[8,14,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Supervised Cervical Exercise Program","EXPERIMENTAL","Participants will perform a supervised cervical and scapular strengthening program focused on deep cervical flexor activation and motor control. The intervention will consist of 12 sessions over six weeks (two sessions per week). Exercises will include cranio-cervical flexion movements, isometric contractions in supine, prone, and side-lying positions, and progressive load adjustments guided by the Borg Rating of Perceived Exertion Scale (target intensity 7\u002F10). Load progression will be implemented after week three to maintain training intensity.",[13],"Other: Supervised Cervical Exercise Program",{"label":15,"type":10,"description":16,"interventionNames":17},"Low-Frequency Transcutaneous Neuromodulation","Participants will receive low-frequency electrical stimulation applied bilaterally over the spinal accessory nerve at Erb's point using the Pointer Excel II device. Stimulation parameters will be set at 4 Hz for 5 minutes per side during each session. The intervention will be delivered twice weekly for six weeks.",[18],"Device: Low-Frequency Transcutaneous Neuromodulation",{"label":20,"type":21,"description":22,"interventionNames":23},"Sham Transcutaneous Neuromodulation","SHAM_COMPARATOR","Participants will undergo a simulated neuromodulation procedure using the same device and positioning as the active neuromodulation group. No electrical current will be delivered. The device will remain in point-detection mode to produce sound without stimulation. The duration and frequency of sessions will match the active intervention group.",[24],"Device: Sham Transcutaneous Neuromodulation",[26,29,32],{"type":6,"name":9,"description":11,"armGroupLabels":27,"otherNames":28},[9],null,{"type":30,"name":15,"description":16,"armGroupLabels":31,"otherNames":28},"DEVICE",[15],{"type":30,"name":20,"description":22,"armGroupLabels":33,"otherNames":28},[20],{"type":35,"investigatorFullName":36,"investigatorTitle":37,"investigatorAffiliation":5,"oldNameTitle":28,"oldOrganization":28},"PRINCIPAL_INVESTIGATOR","Alberto Roldán","Principal Investigator","100627715","effects-of-transcutaneous-neuromodulation-and-cervical-exercise-in-students-with-chronic-nonspecific-cervical-pain-100627715",false,"NCT07452237","Effects of Transcutaneous Neuromodulation and Cervical Exercise in Students With Chronic Nonspecific Cervical Pain","TN-E-CNCP","Inclusion Criteria:\n\n* University students aged 18-30 years\n* Chronic non-specific neck pain lasting ≥ 3 months\n* Pain intensity \\>3\u002F10 on VAS\n* No pharmacological or physiotherapy treatment in the past 3 months\n\nExclusion Criteria:\n\n* Specific cervical pathology (e.g., radiculopathy)\n* Neurological, cardiovascular, systemic, or infectious disease\n* Diagnosed psychological disorders\n* Pregnancy or postpartum period \\\u003C 1 year\n* Regular use of analgesics, opioids, or antidepressants\n* Previous cervical spine or shoulder surgery\n* Electronic implants\n* Neck pain associated with vertigo","ALL","18 Years","30 Years",{"count":49,"type":50},51,"ESTIMATED","INTERVENTIONAL",[53],"NA","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.",[56],"Chronic Non-specific Neck Pain",[58,59,60,61,62,63,64],"Chronic Non-Specific Neck Pain","Neck Pain","University Students","Cervical Exercise","Deep Cervical Flexor Training","Transcutaneous Neuromodulation","Low-Frquency Electrical Stimulation","NOT_YET_RECRUITING","2026-03-05",{"date":68,"type":69},"2026-03-09","ACTUAL",{"date":71,"type":50},"2026-04-01",{"date":73,"type":50},"2026-07-01",{"name":5,"class":6}]