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Effect Of Pressure Biofeedback on Deep Cervical Muscle Training Among University Teachers.

Effects of Pressure Biofeedback on Deep Cervical Flexor Muscle Training for Neck Pain, Functional Disability and Muscle Endurance Among University Teachers. A Randomized Control Trail

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05261854
Enrollment
100
Registered
2022-03-02
Start date
2021-05-01
Completion date
2022-04-05
Last updated
2022-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neck Pain

Keywords

Neck pain, Disabilty, Muscle endurance, Pressure biofeedback, Teachers

Brief summary

The aim of this study is to investigate the effect of pressure biofeedback on deep cervical muscle in university teachers suffering from neck pain, Functional Disability and muscle endurance.

Detailed description

The purpose of this study will be to determine whether training of deep cervical flexor muscles with pressure biofeedback has any significant advantage over conventional training for pain and disability experienced by university teachers with neck pain. This study will be a randomized control trial with double blinded protocol. Patient will be randomly allocated in two groups. the experimental group received deep cervical flexor muscles training with pressure biofeedback and conventional exercises. The control group received deep cervical flexor muscles training with only conventional exercises.

Interventions

Deep cervical flexor training by using preesure biofeedback will be given 5 days a week for 6 week Conventional exercise for deep cervical muscle training will be given 5 days a week for 6 weeks

OTHERConventional exercises for deep cervical muscle training

Conventional exercise for deep cervical muscle training will be given 4 days a week for 6 weeks

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

The study Would be double blind as the identity of patients group will not be revealed to the assessor and the patient will also be unaware of group to which they will be allocated.

Eligibility

Sex/Gender
ALL
Age
24 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Both gender * age between 24 to 45 years * At least 4 years of teaching experience and average 8 hours of working per day * Chronic Neck pain score of more than 5 on numeric pain rating scale * Mild to moderate disability Score on neck disability index

Exclusion criteria

* Participants with any ongoing treatment for neck pain * History of cervical spine surgery or reported any neurological signs. * History of any congenital or acquired postural deformity, spinal cord compression, tumour, instability, fracture, inflammatory disease or infection.

Design outcomes

Primary

MeasureTime frameDescription
Numeric pain rating Scale8th weekNumeric pain rating scale used to determine pain intensity experienced by individuals. It consist of a horizontal or vertical line with total of 11 numbers,ranging from 0 to 10. Where 0 indicates no pain while 10 is the worst pain.
Inclinometer8th weekIt is an instrument used for measuring the angles of tilt,elevation and depression of an object with respect to gravity.
Cranio-cervical flexion test8th weekIt is a clinical test of the anatomical action of the deep cervical flexor muscles. It could be described as a test of neuromotor control. The features assessed are the activation and isometric endurance of the deep cervical flexors
Neck Disability index8th weekThis questionnaire has been designed to give us information as to how your neck pain has affected your ability to manage in everyday life.

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026