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Neck Syndrome clinical trials

View clinical trials related to Neck Syndrome.

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NCT ID: NCT05751070 Completed - Neck Syndrome Clinical Trials

Bowen and Graston Technique in Patients of Tension Neck Syndrome

Start date: March 16, 2023
Phase: N/A
Study type: Interventional

To compare the effects of Bowen and Graston technique in Tension neck syndrome for neck pain , ROM and disability in patients with Tension neck syndrome .

NCT ID: NCT05479279 Completed - Neck Syndrome Clinical Trials

Effectiveness of Neck Stabilization Training Program With Conventional Therapy in Management of Text Neck Syndrome

Start date: September 30, 2021
Phase: N/A
Study type: Interventional

1. To compare the effectiveness of neck stabilization training program with conventional physical therapy in management of neck pain and disability in individuals with text neck syndrome. 2. To compare the effectiveness of neck stabilization training program with conventional physical therapy in improving muscle strength and range of motion of cervical spine in individuals with text neck syndrome.

NCT ID: NCT05249673 Completed - Neck Syndrome Clinical Trials

Global Postural Reeducation Versus Neck Stabilization Training on Text Neck Syndrome.

Start date: January 26, 2022
Phase: N/A
Study type: Interventional

The study will be randomized control trial. The study will be conducted in Iqbal Mehmooda Trust Hospital. Group A will be treated with global postural reeducation. Group B will be treated with neck stabilization training. Non probability consecutive sampling technique will be used. Patient below 20-40 years, participants who use smart phones for 8 hours per day(guidelines), angle of forward head pasture above 15, screening picture tool. Neurological defects, trauma, tumor, shoulder injury, cervical disc disease. REBA questionnaire, NDI, Goniometry, NPRS will be used as a tool. The global postural reeducation will be applied on group A while neck stabilization training will be applied on group B. The aim of this study will be to compare the effects of of global postural reeducation and neck stabilization training on text neck syndrome.

NCT ID: NCT04796051 Completed - Neck Pain Clinical Trials

Comparison Between Effect of Posterior Cervical Weighting and Deep Cervical Flexion Exercise on Forward Head Posture

FHP
Start date: April 10, 2021
Phase: N/A
Study type: Interventional

It has been reported that the head protrudes forward relative to the body from the sagittal plane associated with the anterior shifting of the line of gravity (LOG) relative to the base of support (BOS). On the other hand, the center of gravity (COG) has changed with the forward head posture (FHP) and is related to mechanical and musculoskeletal modifications due to postural control, which affects the whole body balance. Griegel-Morris et al. Reported that, after evaluating eighty-eight healthy participants, 66% had a forward head posture (FHP). In addition, he stated that the inverted head posture in the forward head posture will not only cause neck problems, but also can extend to the shoulder joint and thoracic spine. As a result, it causes a general imbalance in the musculoskeletal system. Jung-Ho Kang and his colleagues examined the effect of daily sitting times of computer users on dynamic and static balance and stated that balance ability decreased in heavy computer users. Another study on forward head posture (IBP) revealed that it limits ankle joint movement, especially in ankle plantarflexion.

NCT ID: NCT04674904 Completed - Neck Syndrome Clinical Trials

Effects of Dry Needling in Patients With Upper Cross Syndrome

Start date: March 30, 2020
Phase: N/A
Study type: Interventional

The study will be done to evaluate the effectiveness of dry needling of muscles involved in Upper Cross Syndrome. Muscles involved in upper cross syndrome are tight upper trap, Levator Scapulae, Sternocledomastoid , Pectorals major and minor and rhomboids. Physical assessment of trigger points will locate the target area for dry needling. After pre treatment measurements, dry needling will be performed to treatment group and stretching, hot pack and tens will be apply in control group. Study design will be randomized controlled trial and sample size will be 34 participants. Data will be collected from Riphah Rehabilitation Center. Patients of 20-50 years old with UCS diagnosed through observation and physical examination will be included. Patients with systemic soft tissue and bony diseases will be excluded. Intervention duration will be two session of DNT with two weeks routine management. Basic tools will be Visual analog scale (VAS), Neck Disability Index (NDI) and Goniometry

NCT ID: NCT04603716 Completed - Neck Syndrome Clinical Trials

Concentric Versus Eccentric Muscle Energy Technique on Upper Cross Syndrome

Start date: December 30, 2019
Phase: N/A
Study type: Interventional

This project was a Randomized control trial conducted to check the effects of eccentric and concentric muscle energy techniques on patients with upper cross syndrome so that we can have best treatment option for patients with upper cross syndrome, duration was of 6months,convenient sampling was done, subject following eligibility criteria from Mansoura hospital female physiotherapy department, Lahore were randomly allocated in two groups via lottery method, baseline assessment was done, Group A participants were given conservative treatment along with eccentric muscle energy technique and Group B participants were given conservative treatment along with concentric muscle energy technique than on 1st,3rdand 6th week post intervention assessment was done via neck disability index, Numeric rating scale, inches tape method,3 sessions per week were given, data was analyzed by using SPSS version 26.

NCT ID: NCT03710785 Completed - Neck Syndrome Clinical Trials

Effect of Neck Extension Exercise Using 8 Channel Surface Electromyography

Start date: October 30, 2017
Phase: N/A
Study type: Interventional

Analysis of Abnormal Muscle Activities on Forward Neck Posture Syndrome Patients and Effect of Neck Extension Exercise Using 8 Channel Surface Electromyography