Cervical Pain

7

Review clinical trials related to Cervical Pain. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Patient Reported Outcome Measurements Registration in Spinal Pathologies and Neuromodulation

Longitudinal prospective observational data collection with questionnaires and categorical diagnostic and therapeutic registration and follow-up in spinal pathologies and neuromodulation

Participants needed: 5,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Jessa HospitalUpdated: Apr 27, 2026Locations: 1
Eligibility criteria

Clinical diagnosis of spinal disease [+3]

Status: Recruiting

Effect Cervical Proprioceptive Training Cervical Proprioception Neck Pain:

Twenty-two male and female patients with neck pain participated in this study, aged from 25-40 years. They randomly distributed into 2 group: group (A, study) consisted of 11 patients received cervical proprioceptive training, while group (B, control) consisted of 11 patients received usual care. The treatment was performed 3 times per week for 1 month. The cervical proprioception (flexion, extension, right and left rotations) was assessed by Revel laser method as active joint angular reproduction \[absolute error\].

Participants needed: 25
Trial details
Age: 25-45Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Jul 10, 2025Locations: 1
Eligibility criteria

they had non-specific neck pain

they had positive spurling test.

Status: Recruiting

Predictors of Response to Manual Physiotherapy Using Somatosensory Profiles in Patients With Cervicobrachial Pain

The goal of this clinical trial is to investigate about the characteristics that predict response to physiotherapy treatment in patients with nerve related neck arm pain. The main question to answer is whether there is a subgroup that responds better to physiotherapy treatment. Participants will be assessed for clinical and neurophysiological characteristics prior to treatment. Afterwards they will receive 6 sessions of manual physiotherapy treatment along with home nerve gliding exercises once a week. Baseline measurements will be taken again after treatment to know if there have been any changes.

Participants needed: 91
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: University of DeustoUpdated: Mar 26, 2025Locations: 1
Eligibility criteria

Subjects with unilateral cervicobrachial pain

Signs of severe disease, cervical myelopathy, tumour, rheumatic diseases or a ne... [+2]

Status: Not yet recruiting

Biomechanical Risk Factors of Cervical Pain in Pregnant Women

The purpose of the study is to assess the biomechanical risk factors for neck pain in pregnant women.

Participants needed: 116
Trial details
Age: 20-35Biological sex: FemaleType: ObservationalSponsor: Cairo UniversityUpdated: Dec 19, 2024Locations: 1
Eligibility criteria

Pregnant women in their third trimester suffering from cervical pain. [+2]

Objective signs of structural pathology on physical examination, including but n... [+6]

Status: Not yet recruiting

Effect of Cervical Stabilization Exercises on Proprioception and Hand Grip Strength in Sedentary Office Workers

The purpose of the study is to evaluate the effect of cervical stabilization exercises on pain intensity level, cervical range of motion, proprioception, and handgrip strength in sedentary office workers.

Participants needed: 52
Trial details
Age: 25-35Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Jul 10, 2024
Eligibility criteria

Age range between 25 and 35 years. [+5]

Unwillingness to participate in the treatment. [+6]

Status: Recruiting

Chitosan Phonophresis on Cervical IN Smartphone Addicted Users

A phonophoresis-based drug delivery system is a synchronous approach to improve local drug penetration in neuromuscular diseases associated with neuronal damage, excruciating pain, and local inflammation. Chitosan, a semi-synthetic material, is obtained by partial deacetylation of chitin amines, resulting in copolymers of N-acetylglucosamine and N-glucosamine. Its use has been explored in various biomaterial and medical applications. Chitosan has emerged as a cost-effective, biocompatible, and biodegradable material with many desirable biological properties, improvement of homeostasis and antiviral potential. Chitosan was found to suppress pro-inflammatory cytokines and decreased peripheral nerve edema, the polycationic nature of chitosan allows it to absorb protons, which reduces inflammation and provides an analgesic effect.

Participants needed: 30
Trial details
Age: 16-18Biological sex: AllType: InterventionalSponsor: October 6 UniversityUpdated: Jul 9, 2024Locations: 1
Eligibility criteria

Their age will be ranged from 16-18 years [+3]

any previous head and neck injuries or surgeries [+4]

Status: Recruiting

Combined Effects of Virtual Reality and Motor Imagery in Patients With Non-specific Neck Pain

Non-specific neck pain is the most common musculoskeletal symptom which can cause limited cervical mobility, impaired functional status and stress at work. Virtual reality and motor imagery are unique technologies which have beneficial effects on the treatment of non-specific neck pain. Virtual reality is a simulated 3D environment that enables users to explore and interact with a virtual surrounding while motor imagery (MI) is a dynamic mental process of an action, without its actual motor execution. This study aims to investigate the combined effects of Virtual Reality (VR) and Motor Imagery Techniques (MI) with Routine Physical Therapy (RPT) in patients with Non-specific neck pain. This randomized clinical trial will be carried at Railway General Hospital, Rawalpindi on 93 participants meeting the inclusion criteria included in the study through probability convenience sampling technique. 3 groups of participants assigned ramdomly will receive interventions for three days a week for 6 weeks. Group A will receive virtual reality (VR) and motor imagery (MI) along with routine physical therapy for . Group B participants will receive VR along with routine physical therapy while Group C will receive MI along with routine physical therapy. Total treatment time will be 40 minutes. Outcome measure tools will be Numeric pain rating scale to measure pain, the Tampa scale of Kinesiophobia (TSK) for the measurement of kinesiophobia and Neck disability index for disability and functional status.

Participants needed: 93
Trial details
Age: 18-50Biological sex: AllType: InterventionalSponsor: Riphah International UniversityUpdated: Jun 13, 2024Locations: 1
Eligibility criteria

Age of the patients should be 18-50 years [+3]

Specific neck pain caused by metastasis, neoplasia, infectious or inflammatory d... [+8]