Comparative Effects of Cervical Stabilization and Isometric Neck Exercises in Eyeglass Wearers With Non-specific Chronic Neck Pain

December 22, 2025 updated by: Ibadat International University, Islamabad

Comparative Effects of Cervical Stabilization and Isometric Neck Exercises on Pain, Disability, Quality of Life and Kinesiophobia in Eyeglass Wearers With Non-specific Chronic Neck Pain: A Randomized Controlled Trial

The goal of this randomized controlled trial is to compare the effects of cervical stabilization exercises and isometric neck exercises on pain, disability, quality of life, and kinesiophobia in eyeglasses wearers with Non-specific chronic neck pain. Participants were randomly assigned to either Group A (Isometric Neck Exercises) or Group B (Cervical Stabilization Exercises) using a toss-and-trial method.

The intervention was provided over four weeks, with three sessions per week (total of 12 sessions):

Group A (Isometric Neck Exercises): Participants performed isometric neck flexion, extension, lateral flexion, and rotation. Each movement was hold for 10 seconds, repeated 5 times, with a 5-second rest between repetitions.

Group B (Cervical Stabilization Exercises): Participants performed chin tucks, neck extensions, shoulder shrugging, shoulder rolling, and scapular retractions in a sitting position. Each exercise was performed 15 repetitions, 1 set, holding a 6-second contraction followed by 2 seconds of relaxation per repetition.

Study Overview

Detailed Description

Non-specific neck pain, a common disorder of the musculoskeletal system, frequently manifests as discomfort and stiffness in the lateral and posterior aspects of the neck, often lacking distinctive diagnostic indicators.(1) Young adults are disproportionately affected by neck pain, with a significant proportion, between 42% and 67%, experiencing episodes within a one-year period. Notably, the Global Burden of Disease Study identifies neck pain, in tandem with low back pain, as the second most prevalent cause of disability among young adults aged 20-24, resulting in substantial years lived with disability.(2) Kinesiophobia refers to an excessive and debilitating fear of physical movement, stemming from a perceived vulnerability to pain or re-injury. This phenomenon is closely linked to pain catastrophizing, a cognitive and emotional response characterized by exaggerated negative thoughts and feelings about pain. In individuals experiencing chronic pain, pain catastrophizing can lead to a vicious cycle of increased pain perception, disability, and worsening impairment. Initially, these coping mechanisms may provide temporary relief during acute pain episodes. However, when pain persists, they can become maladaptive, perpetuating a cycle of fear, avoidance, and distress.(3) Wearing eyeglasses can significantly influence head and neck posture, as the body compensates for a reduced visual field by adjusting alignment. This compensatory mechanism may lead to chronic postural changes, including forward head posture and deep neck flexor weakness. The likelihood of developing forward head posture increases with the duration of eyeglasses use, highlighting the importance of assessing visual devices as part of patient care, especially when addressing neck pain and functional limitations.

Exercise plays a vital role in managing neck pain by restoring tissue function and maintaining daily activities. Research has demonstrated that targeted exercises, such as isometric and cervical stabilization exercises, can effectively reduce pain, improve muscle performance, and enhance endurance. Neck stabilization exercises improve joint mobility, sensorimotor function, and relaxation, while isometric exercises strengthen weak muscles through proprioceptive engagement. This study aims to compare the therapeutic effects of cervical stabilization versus isometric neck exercises on pain, disability, quality of life, and kinesiophobia in eyeglass wearers with non-specific chronic neck pain, providing insights into the most effective exercise approach for this population.

Study Type

Interventional

Enrollment (Actual)

62

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Islamabad, Pakistan
        • Faculty of Allied Health & Biological Sciences

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

Adults aged 25-50 years, using any form of eyeglasses for more than 2 years, with active non-specific chronic (more than three months) neck pain with pain intensity ≥ 5/10 on the numeric pain rating scale were included.

Exclusion Criteria:

  • Participants with cognitive impairments or limitations that could impact their ability to provide informed consent or adhere to the study protocol.
  • Individuals with a history of cardiovascular, pulmonary, or endocrine disease that could pose a risk to their health during exercise.
  • Participants with health conditions that may prevent them from engaging in physical activity, such as severe musculoskeletal disorders or neurological impairments.
  • Individuals with red flag symptoms indicative of underlying serious pathology, such as recent trauma, infection, or malignancy.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Isometric Neck Exercises
Participants received isometric neck exercises (Isometric neck flexion, Isometric neck extension, Isometric lateral flexion and rotation), holding each movement for 10 s, and repeating each 5 times with a 5-s rest between each of them
Intervention Group A (Isometric Neck Exercises Group) Group A participants received isometric neck exercises (Isometric neck flexion, Isometric neck extension, Isometric lateral flexion and rotation), holding each movement for 10 s, and repeating each 5 times with a 5-s rest between each of them.
Experimental: Cervical Stabilization Exercises
Participants received each neck stabilization exercises (Tucking in of chin, extending the neck, shrugging of shoulder, rolling of shoulder, retraction of scapular) in sitting position with a frequency of 15 repetitions 1 set with relaxation maintaining 6 seconds of contraction followed by 2 seconds of relaxation per repetition.
Intervention Group B (Cervical Stabilization Exercises Group) Group B participants received each neck stabilization exercises (Tucking in of chin, extending the neck, shrugging of shoulder, rolling of shoulder, retraction of scapular) in sitting position with a frequency of 15 repetitions 1 set with relaxation maintaining 6 seconds of contraction followed by 2 seconds of relaxation per repetition.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Neck Pain
Time Frame: Assessment was done at baseline, Week 2 and Week4
Pain was measured by NPRS
Assessment was done at baseline, Week 2 and Week4
Disability
Time Frame: Assessment was done at baseline, Week 2 and Week4
Disability was measured by Neck Disability Index
Assessment was done at baseline, Week 2 and Week4
Kinesiophobia
Time Frame: Assessment was done at baseline, Week 2 and Week4
Kinesiophobia was measured by Tempa Scale-11
Assessment was done at baseline, Week 2 and Week4

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Quality of life of Patients having Neck pain
Time Frame: Assessment was done at baseline, Week 2 and Week4
Quality of life was measured by SF-12
Assessment was done at baseline, Week 2 and Week4

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Muhammad Nazim Farooq, PhD-PT, Ibadat International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 26, 2025

Primary Completion (Actual)

October 27, 2025

Study Completion (Actual)

October 27, 2025

Study Registration Dates

First Submitted

December 22, 2025

First Submitted That Met QC Criteria

December 22, 2025

First Posted (Actual)

January 6, 2026

Study Record Updates

Last Update Posted (Actual)

January 6, 2026

Last Update Submitted That Met QC Criteria

December 22, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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