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CompletedNCT05026086Updated Apr 22, 2022

Isometric Exercises With and Without Pressure Biofeedback in Computer Users With Cervical Spine Overload

An interventional study of pressure biofeedback and isometric exercises in Pain, Neck, sponsored by Riphah International University. Completed at 1 site in Pakistan. Open to participants aged 20 Years to 40 Years. Per ClinicalTrials.gov, last updated 2022-04-22.

Sponsored by Riphah International University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
20 Years to 40 Years
Sex
All
01

Study summary

Neck pain is defined as the pain experienced from the base of the skull or occiput to the upper part of the back and extending laterally to the outer and superior bounds of the shoulder blade. Office work is a kind of job that demands sitting for prolonged time requiring the use of computer. These two factors are mainly responsible for overloading of the spine. Neck pain and computer users are clearly connected due to extended periods of sitting in a certain position with no breaks to stretch the neck muscles. Prolonged computer use with neck bent forward will cause the anterior neck muscles to gradually get shorter and tighter, while the muscles in the back of neck will grow longer and weaker. These changes will lead to development of neck pain. Neck problem also accounts for a large proportion of occupational illness and disability. Neck pain is common among computer workers in our country and contributes importantly to the demand for medical services and the economic burden of absence from work due to sickness.

The main purpose of this randomized clinical trial will be to find out the effects of Isometric exercises with and without Pressure Biofeedback Unit on Cervical pain and Muscle strength in Computer users with cervical spine overload. Patients will be recruited in the study by convenient sampling technique after that will be allocated to groups by simple random assignment with an inclusion criteria having chronic neck pain for more than 3 months, current pain level ranging greater than 3 on NPRS, patient with minimum and moderate disability and male and female computer users with age 25 to 40 years with cervical pain. Patients with history of cervical trauma, postural deformity, spinal cord deformity, current pregnancy and significant neurological deficits were excluded.

Numeric Pain Rating Scale (NPRS) and Neck Disability Index (NDI) will be used to measure before and after treatment session. Treatment will be given to both groups for 4 weeks and each group will receive 3 sessions per week. After collecting the data it will entered and analysed using Statistical Package for the Social Sciences (SPSS) version 25. Data will be assessed by using parametric/ non parametric test after completion of the study.

02

Conditions studied

  • Pain, Neck

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03

In context

Neck Pain

1,232 studies on the registry are indexed under Neck Pain; 254 are open to participants now.

This study's enrollment of 20 is below the median of 52 across 1,004 interventional studies indexed under Neck Pain.

Browse Neck Pain studies →

Lead sponsor

Riphah International University is the lead sponsor of 2,133 studies on the registry; 633 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Aged between 20-40 years among male and female with cervical pain
  • Having chronic pain for more than 3 months.
  • Current pain level ranging greater than 3 on NPRS
  • Patients with minimum and moderate disability based on NDI

Exclusion criteria

Exclusion Criteria:

  • History of cervical trauma
  • Postural deformity
  • Spinal cord deformity ( scoliosis, kyphosis, lordosis)
  • Current pregnancy
  • Significant neurological deficits ( cervical radiculopathy, cervical spondylosis)
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
20 participants (actual)

Study arms

  • Experimental
    biofeedback

    10 patients will be treated with isometric exercises and pressure biofeedback.

    Other: pressure biofeedback

  • Active comparator
    isometric exercises

    10 patients will be treated with isometric exercises without pressure biofeedback.

    Other: isometric exercises

Interventions

  • Otherpressure biofeedback

    10 patients will be treated with isometric exercises and pressure biofeedback.

  • Otherisometric exercises

    10 patients will be treated with isometric exercises

06

What researchers measure

Primary outcomes

  1. pain of patient

    NPRS The Numerical Pain Rating Scale (NPRS) is a subjective measure in which individuals rate their pain on an eleven-point numerical scale. The scale is composed of 0 (no pain at all) to 10 (worst imaginable pain).

    Time frame: 4 weeks

  2. function

    Neck Disability index (NDI) Item scores range from 0 to 5, and the total score is a total of the item scores (possible range 0 (no pain) - 100 (maximal pain)

    Time frame: 4 weeks

07

Study locations

1 site
  • Muhammad Hahim
    Lahore, Ppunjab 54000, Pakistan
08

References and documents

Publications

  • Cohen SP, Hooten WM. Advances in the diagnosis and management of neck pain. BMJ. 2017 Aug 14;358:j3221. doi: 10.1136/bmj.j3221. PubMed 28807894 ↗
  • Barrett JM, McKinnon C, Callaghan JP. Cervical spine joint loading with neck flexion. Ergonomics. 2020 Jan;63(1):101-108. doi: 10.1080/00140139.2019.1677944. Epub 2019 Oct 15. PubMed 31594480 ↗
  • Genebra CVDS, Maciel NM, Bento TPF, Simeao SFAP, Vitta A. Prevalence and factors associated with neck pain: a population-based study. Braz J Phys Ther. 2017 Jul-Aug;21(4):274-280. doi: 10.1016/j.bjpt.2017.05.005. Epub 2017 May 20. PubMed 28602744 ↗
  • Khan R, Surti A, Rehman R, Ali U. Knowledge and practices of ergonomics in computer users. J Pak Med Assoc. 2012 Mar;62(3):213-7. PubMed 22764450 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 22, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05026086
Lead sponsor
Riphah International University
Responsible party
Sponsor
First posted
Aug 30, 2021
Start date
Aug 5, 2021
Primary completion
Feb 28, 2022
Completion
Feb 28, 2022
Last update
Apr 22, 2022

Study contacts

Muhammad Salman Bashir, PhD
principal investigator · Riphah International University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Apr 2022. You cannot join it, but the record below documents what was studied.

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