- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06947421
The Effect of Different Exercises on Craniovertebral Angle in Individuals With Forward Head Posture
Effectiveness of McKenzie and Standard Neck Exercises on Craniovertebral Angle, Hand Grip Strength, and Psychosocial Status in Individuals With Forward Head Posture- Randomized Assessor Blinded Clinical Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Forward head posture (FHP) is a common postural misalignment characterized by the anterior positioning of the head relative to the trunk in the sagittal plane. It is frequently associated with poor ergonomic habits, prolonged screen time, heavy backpack use, and lack of physical activity. This postural deviation can lead to upper cervical hyperextension, lower cervical and upper thoracic flexion, increased muscle tension, and long-term dysfunctions in the musculoskeletal, neurological, and vascular systems.
The craniovertebral angle (CVA) is a commonly used and reliable method for evaluating FHP. A CVA less than 50 degrees is considered indicative of forward head posture. Current literature supports the use of exercise interventions to improve CVA and reduce the symptoms associated with postural abnormalities.
The McKenzie method is based on directional preference and repetitive movements, aiming to enhance postural awareness and spinal alignment. Standard neck exercises, frequently used in clinical practice, aim to improve muscular balance, cervical alignment, and reduce neck pain.
Although both exercise methods have shown individual effectiveness in improving posture and function, few studies have directly compared their effects on both structural and functional outcomes. Additionally, hand grip strength and psychosocial factors are often overlooked, despite their importance in evaluating upper extremity function and overall well-being in individuals with FHP.
This randomized, assessor-blinded clinical trial aims to compare the short-term effects of McKenzie exercises and standard neck exercises on craniovertebral angle, hand grip strength, and psychosocial status in individuals with forward head posture. The results will contribute to clinical knowledge regarding effective rehabilitation strategies for postural dysfunctions.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Bursa, Turkey, 16940
- Mudanya University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Individuals diagnosed with forward head posture, defined by a craniovertebral angle (CVA) of less than 50°, based on established diagnostic criteria
- Age between 18 and 30 years
- Pain intensity greater than 3 on the Visual Analog Scale (VAS)
- Mild to moderate neck disability, indicated by a Neck Disability Index (NDI) score below 15 out of 50
- Voluntary participation with signed informed consent
Exclusion Criteria:
- Presence of medical contraindications to exercise
- Regular engagement in structured spinal exercise programs
- History of spinal surgery
- Diagnosis of cancer or other malignant conditions
- Presence of an implanted cardiac pacemaker
- Visual, auditory, or cognitive impairments that would prevent adherence to the exercise protocol
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: McKenzie Exercise Group (MG)
Participants in this group will follow a McKenzie-based cervical exercise program consisting of four specific movements: retraction, rotation, lateral flexion, and combined rotation.
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Exercises will be performed in seated or supine positions, 15 repetitions per session, twice daily, for a total duration of 6 weeks. The program will begin with physiotherapist-supervised sessions and continue at home with guidance via a digital training manual. Weekly follow-up and progress will be ensured through individual exercise diaries. Participants missing two consecutive days of exercise will be excluded from the study. Includes:
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Experimental: Standard Neck Exercise Group (SG)
Participants in this group will follow a standard cervical postural correction program focused on strengthening deep cervical flexors and scapular retractors, and stretching cervical extensors and pectoralis muscles.
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The protocol includes chin tucks, chin drop stretches, scapular retraction with resistance, and both unilateral and bilateral pectoral stretching. Exercises will be performed twice daily, 15 repetitions per session, over a period of 6 weeks. Exercise progression will be adapted biweekly based on participant tolerance. Includes:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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1.Craniovertebral Angle (CVA)
Time Frame: through study completion, an average of 6 months
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CVA is used to assess forward head posture. Participants will be asked to stand in a natural and relaxed posture while focusing on a marked point at eye level on the wall. A lateral photograph will be taken using a Iphone 13 camera mounted on a tripod at shoulder height and placed 1.5 meters from the participant. The spinous process of the C7 vertebra and the tragus of the ear will be marked. The angle between the line connecting the tragus to C7 and a horizontal reference line will be calculated using the ImageJ software. The measurement results will be recorded on the evaluation form. Analysis Metric: Change in CVA (degrees) |
through study completion, an average of 6 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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2.Cognitive Exercise Therapy Approach Scale (BETY)
Time Frame: through study completion, an average of 6 months
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The BETY scale will be used to assess participants' biopsychosocial status, including emotional state, functionality, fatigue, pain, sleep quality, and social/sexual life. The scale consists of 30 items scored on a 0-4 Likert scale, with a total score range of 0-120. Higher scores indicate greater biopsychosocial impairment. Analysis Metric: Total score (0-120) |
through study completion, an average of 6 months
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3.Hand Grip Strength (HGS)
Time Frame: through study completion, an average of 6 months
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Grip strength will be measured using a Baseline hydraulic hand dynamometer. Participants will be seated or standing upright with the shoulder in adduction, elbow at 90° flexion, wrist in 0-30° extension and 0-5° ulnar deviation. They will be instructed to squeeze the dynamometer with maximum effort for 3 seconds. The test will be performed three times for each hand (starting with the dominant hand), and the highest value from each will be recorded. Analysis Metric: Maximum grip strength in kilograms (kg) |
through study completion, an average of 6 months
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4.Neck Disability Index (NDI)
Time Frame: through study completion, an average of 6 months
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The Neck Disability Index is a standardized self-reported questionnaire used to assess the impact of neck pain on daily living activities.
This scale evaluates the individual's functional status through self-assessment of neck pain, including domains such as pain intensity, personal care, lifting, reading, headaches, concentration, work, driving, sleeping, and recreational activities.
Each section is scored on a scale from 0 ("no pain") to 5 ("the worst pain imaginable").
The scores from each section are summed and expressed as a percentage to determine the overall level of disability.
Interpretation categories are as follows: 0-8% = no disability, 10-28% = mild, 30-48% = moderate, 50-64% = severe, and 70-100% = complete disability
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through study completion, an average of 6 months
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5. Visual Analog Scale (VAS) for Neck Pain
Time Frame: through study completion, an average of 6 months
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Cervical pain intensity will be assessed using a 10-cm horizontal VAS.
Participants will mark their current level of pain on the line, where 0 indicates "no pain" and 10 indicates "worst imaginable pain."
Analysis Metric: Pain score (0-10)
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through study completion, an average of 6 months
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Pelin Pişirici, PhD, Bahcesehir University, Faculty of Health Sciences, Department of Physiotherapy
- Principal Investigator: Esra Beceni, PhD Student, Bahcesehir University, Graduate Education Institute
- Study Chair: Büşra Tamgüç, PhD Student, Bahcesehir University, Graduate Education Institute
- Study Chair: Gülay Yalcin, PhD, Mudanya University, Faculty of Health Sciences, Department of Physiotherapy
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- E-10840098-202.3.02-2206
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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