Comparative Effects of Cervical Stabilization and Isometric Neck Exercises in Eyeglass Wearers With Non-specific Chronic Neck Pain
1 other identifier
interventional
62
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started May 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 26, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 27, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
October 27, 2025
CompletedFirst Submitted
Initial submission to the registry
December 22, 2025
CompletedFirst Posted
Study publicly available on registry
January 6, 2026
CompletedJanuary 6, 2026
December 1, 2025
5 months
December 22, 2025
December 22, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Neck Pain
Pain was measured by NPRS
Assessment was done at baseline, Week 2 and Week4
Disability
Disability was measured by Neck Disability Index
Assessment was done at baseline, Week 2 and Week4
Kinesiophobia
Kinesiophobia was measured by Tempa Scale-11
Assessment was done at baseline, Week 2 and Week4
Secondary Outcomes (1)
Quality of life of Patients having Neck pain
Assessment was done at baseline, Week 2 and Week4
Study Arms (2)
Isometric Neck Exercises
ACTIVE COMPARATORParticipants 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
Cervical Stabilization Exercises
EXPERIMENTALParticipants 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.
Interventions
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.
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.
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Faculty of Allied Health & Biological Sciences
Islamabad, Pakistan
Related Publications (3)
Asiri F, Reddy RS, Tedla JS, ALMohiza MA, Alshahrani MS, Govindappa SC, Sangadala DR. Kinesiophobia and its correlations with pain, proprioception, and functional performance among individuals with chronic neck pain. PLoS One. 2021 Jul 8;16(7):e0254262. doi: 10.1371/journal.pone.0254262. eCollection 2021.
PMID: 34237105BACKGROUNDJahre H, Grotle M, Smedbraten K, Dunn KM, Oiestad BE. Risk factors for non-specific neck pain in young adults. A systematic review. BMC Musculoskelet Disord. 2020 Jun 9;21(1):366. doi: 10.1186/s12891-020-03379-y.
PMID: 32517732BACKGROUNDBernal-Utrera C, Gonzalez-Gerez JJ, Anarte-Lazo E, Rodriguez-Blanco C. Manual therapy versus therapeutic exercise in non-specific chronic neck pain: a randomized controlled trial. Trials. 2020 Jul 28;21(1):682. doi: 10.1186/s13063-020-04610-w.
PMID: 32723399BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Muhammad Nazim Farooq, PhD-PT
Ibadat International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Masking Details
- This randomized controlled trial was double-blinded. Participants were randomly assigned to either the Cervical Stabilization Exercise group or the Isometric Neck Exercise group using a simple randomization (coin toss) method. Participants were informed that both interventions were effective physiotherapy treatments for chronic neck pain but were not told which group they belonged to. The outcome assessor, who had over fifteen years of experience, remained blinded to group allocation throughout data collection at baseline, week 2, and week 4. To maintain blinding, participants were instructed not to disclose their exercise details during assessment, and all data were recorded using coded identifiers (Group A or B).
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 22, 2025
First Posted
January 6, 2026
Study Start
May 26, 2025
Primary Completion
October 27, 2025
Study Completion
October 27, 2025
Last Updated
January 6, 2026
Record last verified: 2025-12