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Comparison of Craniocervical Flexion and Scapular Stabilization Exercises in Forward Head Posture and Neck Pain

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ClinicalTrials.gov Identifier: NCT04557904
Recruitment Status : Completed
First Posted : September 22, 2020
Last Update Posted : September 22, 2020
Sponsor:
Information provided by (Responsible Party):
Riphah International University

Brief Summary:
The aim of this research is to compare the effects of craniocervical flexion exercises and scapular stabilization exercises in reducing neck pain and forward head posture among females wearing head scarves. Quasi experimental trials done at Akhtar Saeed Trust hospital, Falah o Behbud Associations and Medicare Hospital (Lahore, Pakistan). A sample size of 50 patients was taken using non-probability purposive sampling technique. Subjects were randomly divided into 2 groups. Subjects in group A were treated with craniocervical flexion exercises and the subjects in group B were treated with scapular stabilization exercises with 25 subjects in each group. Pretreatment evaluation was done using numeric pain rating scale (NPRS) and neck disability index (NDI) as subjective measurement and Goniometry for assisted range of motion (AROM) and plumb line method for measuring head posture as objective measurement. The baseline values for all dependent variables were recorded on day one and at the end of 4th week.

Condition or disease Intervention/treatment Phase
Cervical Pain Other: Craniocervical flexion exercises Other: Scapular stabilization exercises Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 50 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Effects of Craniocervical Flexion Exercises and Scapular Stabilization Exercises in Neck Pain and Forward Head Posture Among Female Wearing Head Scarves
Actual Study Start Date : June 15, 2018
Actual Primary Completion Date : February 20, 2019
Actual Study Completion Date : March 15, 2019

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Group A: Craniocervical flexion exercises
Exercise protocol were performed over a 4 week duration under the command of a supervisor. Subjects were asked not to obtain any other particular intervention for cervical ache. Command the subject to be in crook lying position. Lock their finger to place their finger below the skull and retract the lower jaw and retract chin as far as possible.
Other: Craniocervical flexion exercises
Command the subject to be in crook lying position. Lock their finger to place their finger below the skull and retract the lower jaw and retract chin as far as possible. Subject has to slightly raise his/he skull a few centimeters. Fingers should be touching the cranium but not supporting it. Subject had to respire and hold the position. Subject has the move out the chin. Stop exercise and restart again. Perform this exercise for 10 times by holding this position for 20 sec at the start of the exercise, increasing it by 10 seconds every session commonly underwent pectoralis minor stretching before every session of exercise of 4 sets with 30 second's hold

Experimental: Group B: Scapular stabilization exercises
Group B performed scapular stabilization workout for 30 minutes per session, three days a week for four weeks. The scapular stabilization exercises were made up of four stages
Other: Scapular stabilization exercises
The scapular stabilization exercises were made up of four stages: (1) In supine position, the patient was commanded to deep respire for the sake of relaxation by maintain the cervical and shoulder in relaxing position to take a deep breath to relax the body while holding her shoulders and neck in relaxing position. (2) The patient then flex her knees and placed her feet flat on the plinth, and maintain the pose without any cervical movement. Then the patient asked to raise her dominant arm to 90° shoulder flexion with full elbow extension and scapular protraction. This position was sustained for 10 seconds before going to initial position. Three laps of 10 repetitions with one-minute interval in between were performed. (3) In quadruped position, the patient raise her arms alternatively with shoulder abduction and 120 ° flexion. That posture was held for 10 seconds before returning to the starting position. (4) In sitting position




Primary Outcome Measures :
  1. Neck disability index [ Time Frame: 4th week ]
    Changes from base line Northwick disability index was developed first in Northwick Park hospital, England. It was designed to measure the neck pain and disability over time. It consists of 10, five parts sections. At the end, score is calculated by dividing the obtained score by total (50) multiplied by 100. As the driving section was missing in all the female patients, total score was considered as 45 instead of 50

  2. Numeric Pain Rating Scale [ Time Frame: 4th week ]
    Changes from base Line Numeric Pain rating scale is a scale for pain starting from 0-10. where 0 indicate no pain and 10 indicate severe pain.

  3. ROM Cervical Spine ( Flexion) [ Time Frame: 4th week ]
    Changes from the Baseline ROM range of Motion of Cervical spine flexion was taken with the Help of Goniometer

  4. ROM Cervical Spine ( extension) [ Time Frame: 4th week ]
    Changes from the Baseline ROM range of Motion of Cervical spine extension was taken with the Help of Goniometer

  5. ROM Cervical Spine ( Right side flexion) [ Time Frame: 4th week ]
    Changes from the Baseline ROM range of Motion of Cervical spine right side flexion was taken with the Help of Goniometer

  6. ROM Cervical Spine ( left side Flexion) [ Time Frame: 4th week ]
    Changes from the Baseline ROM range of Motion of Cervical spine left side flexion was taken with the Help of Goniometer

  7. ROM Cervical Spine ( right rotation) [ Time Frame: 4th week ]
    Changes from the Baseline ROM range of Motion of Cervical spine right rotation was taken with the Help of Goniometer

  8. ROM Cervical Spine ( left rotation) [ Time Frame: 4th week ]
    Changes from the Baseline ROM range of Motion of Cervical spine left rotation was taken with the Help of Goniometer

  9. Plumb Line [ Time Frame: 4th week ]
    Participants were requested to wear the suitable attire to properly expose the areas being examined e.g thoracic & cervical spine. The lobe of ear, the seventh cervical vertebra, acromion process, the thoracic spine and lateral malleolus were used as landmarks for measuring the head posture



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Ages Eligible for Study:   20 Years to 40 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Forward-head-posture
  • Duration of wearing-the headscarf/hijab for a minimum of 5-years
  • Females ho start wearing headscarf before or at the age of-20. Females having neck-pain for less-than-six-months or if they had any muscular spasm & tenderness in the neck region.
  • Pain being experienced in cervical spine area, which started from-superior-nuchal line-to the first thoracic vertebra.
  • Pain radiating with or without any extensive radicular-symptoms towards other areas of body such as head and upper extremities.
  • Restricted range-of-motion of cervical-spine.

Exclusion Criteria:

  • Any red flags (tumor, osteoporosis, metabolic disorders, fracture, rheumatoid arthritis, resting-blood-pressure higher than 140/90 mmHg, prolonged-history of steroids abuse, continuous nerve root entrapment with two-or more-positive-neurologic-signs (muscle weakness involving cervical myotomes, abnormal upper limb deep-tendon-reflexes, or- -abnormal cervical dermatome.
  • Already diagnosed with cervical spine-stenosis, showed bilateral upper limb symptoms.
  • Any six weeks prior history of whiplash-injury or engaged in any type of treatment regarding neck pain from any-practitioner within the last month.
  • History-of any previous-cervical or thoracic-spine-surgery-

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04557904


Locations
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Pakistan
Akhtar Saeed Trust hospital, Falah o Behbud Associations and Medicare Hospital
Lahore, Punjab, Pakistan, 54000
Sponsors and Collaborators
Riphah International University
Investigators
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Principal Investigator: Rabiya Noor, PHD Riphah International University
Publications:

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Responsible Party: Riphah International University
ClinicalTrials.gov Identifier: NCT04557904    
Other Study ID Numbers: REC/18/1006 Sanjeela Abbas
First Posted: September 22, 2020    Key Record Dates
Last Update Posted: September 22, 2020
Last Verified: September 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Riphah International University:
Forward head posture, Craniocervical flexion exercises
Additional relevant MeSH terms:
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Neck Pain
Pain
Neurologic Manifestations