Effect of Lumber Core Stability Exercises on Chronic Non-specific Neck Pain

Neck Pain Clinical Trial

Official title:

Effect of Adding Lumbar Core Stability Exercises to Cervical and Scapular Stabilization Exercises and Advices on Chronic Non- Specific Neck Pain

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05712239
• Other study ID #: P.T.REC/012/003950
• Status: Recruiting
• Phase: N/A
• Start date: February 5, 2023
• Est. completion date: April 1, 2024

Study information

• Verified date: August 2023
• Source: Cairo University
• Contact: Hend W Mostafa, MSc
• Phone: 00201004225661
• Email: hendwageh.95[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Chronic non-specific neck pain patients will be enrolled in 3 groups in this study including passive, active control and experimental groups to determine the effect of adding lumbar core stability exercises to patient's advices and cervical and scapular stabilization exercises. For the last two groups, the sessions will be applied 3 times per week for 4 weeks. All the outcomes will be measured after patient's enrollment and at the end of 4 weeks to determine the difference between groups.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 66
• Est. completion date: April 1, 2024
• Est. primary completion date: February 1, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 40 Years

Eligibility

Inclusion Criteria:

• Patients with persistent cervical pain for more than 12 weeks without specific diagnosis (chronic non-specific neck pain).

• BMI less than 30 kg/m2.

• Pain intensity on VAS should be more than 3.

• Patient will be able and motivated in completing the study.

• Psychologically & mentally stable.

Exclusion Criteria:

• Red Flag's symptoms including a history of major trauma, persistent night pain, bladder or bowel dysfunction, and/or lower or upper extremity neurological deficit.

• Pregnant women.

• Recent or old fractures at spine or upper limbs.

• Congenital, or acquired postural deformity.

• No previous neck or spinal or shoulder surgery.

• No current pathologies (e.g. Disc lesion, nerve root compression, canal stenosis, spinal tumor, spinal infection, systemic inflammatory diseases, …).

Related Conditions & MeSH terms

• Neck Pain

Intervention

Other:
• Advices
The advices will include patient's reassurance and description of possible causes of neck pain such as poor working ergonomics, common bad postures especially while using electronic devices for long periods and not adjustable sleeping pillows. Also, patient will be educated how to modify these different causes and asked to apply gentle neck range of motion exercises
• Cervical and Scapular Stabilization Exercises
Deep neck flexor training will be performed in neurodevelopment stages (supine at first week using pressure biofeedback unit , prone at second week, quadrupedal at third week, bipedal at fourth week). Scapular stabilization exercises will include modified prone cobra, trapezius muscle exercise progression (3 stages), wall press and extension of the thoracic spine using foam roller. The modified prone cobra and the first stage of trapezius muscle exercise progression will be applied during the first two weeks. The second and third stages of trapezius muscle exercise will be applied during the last two weeks of our rehabilitation program. All exercises will be applied for 10 repetitions with 6-10 sec hold for 3 sets with 20 sec rest between each set. While wall press and thoracic extension exercises will be applied throughout the 4 weeks for 3 sets of 10 repetitions with 20 sec rest between each set.
• Lumber Core Stability Program
The program will be performed in three stages: activation, dynamic stabilization, and advanced core strengthening stages. Each stage will be applied for 4 sessions. The activation stage will be based on the learning to activate transversus abdominis muscle from crock lying position using pressure biofeedback unit. In the dynamic stabilization stage, the patient will be instructed to slowly raise both arms in the scapular plan then return to the sides while maintaining the transversus abdominis muscle activation. Also, the patient will apply bridging exercise in this stage. The advanced core strengthening stage will include prone plank and side plank (right and left sides). All the exercises will be applied for 10 repetitions with 6-10 sec hold for 3 sets. The rest of 20 sec will be taken between each set.

Locations

Country	Name	City	State
Egypt	Faculty of Physical Therapy, Cairo University	Giza

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	change in pain intensity	Pain intensity will be assessed by using Visual analogue scale (VAS). It is horizontal line with 10 cm length, with Zero marked at one end representing no pain and 10 marked at the other end representing worst imaginable pain.	This outcome will be assessed at the first day and after 4 weeks following end of treatment
Primary	change in functional disability	Functional disability will be assessed using Arabic version of neck disability index. The patients will be asked to make a mark in each section which most closely described their problem. Each section consists of six potential responses for each item ranging from no disability (0) to total disability (5). Thus, The NDI score ranges between 0-100, with higher scores indicating greater perceived disability. The score of less than 4 indicates no disability, 5-14 mild disability, 15-24 moderate disability, 25-34 severe disability, and scores greater than 35 complete disabilities.	This outcome will be assessed at the first day and after 4 weeks following end of treatment
Secondary	change in Craniovertebral angle degree (CVA)	To measure CVA, the patient will be captured from the left side after putting landmarks on seventh cervical vertebra (c7) and tragus of the ear. The photograph will be taken and analyzed with kinovea software by drawing a horizontal line passing through C7 and line connecting between the tragus of the ear and C7 and measuring the angle between these lines. As the value of CVA decreases, the degree of FHP increases	This outcome will be assessed at the first day and after 4 weeks following end of treatment
Secondary	change of of deep neck flexor muscles (DNF) activation	DNF activation will be assessed by Craniocervical flexion test using Pressure biofeedback unit	This outcome will be assessed at the first day and after 4 weeks following end of treatment
Secondary	change of deep neck flexor (DNF) endurance	DNF endurance will be assessed by Neck flexor endurance test	This outcome will be assessed at the first day and after 4 weeks following end of treatment
Secondary	change of trunk flexor muscle endurance	Trunk flexor muscle endurance will be assessed by Trunk flexion test (McGill's test)	This outcome will be assessed at the first day and after 4 weeks following end of treatment
Secondary	change of trunk extensor muscle endurance	Trunk extensor muscle endurance will be assessed by Trunk extension test (Sorenson Test)	This outcome will be assessed at the first day and after 4 weeks following end of treatment
Secondary	change of lateral trunk muscle endurance	Lateral trunk muscle endurance will be assessed Side plank test for left and right sides	This outcome will be assessed at the first day and after 4 weeks following end of treatment