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CompletedNCT05261854Updated Jun 22, 2022

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

An interventional study of Pressure biofeedback and Conventional exercises for deep cervical muscle training in Neck Pain, sponsored by Riphah International University. Completed at 1 site in Pakistan. Open to participants aged 24 Years to 45 Years. Per ClinicalTrials.gov, last updated 2022-06-22.

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

From the registry’s dates

  • Registered 9 months after the study started (first participant enrolled May 2021, registered Feb 2022).
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
24 Years to 45 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Neck Pain

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Keywords

  • Neck pain
  • Disabilty
  • Muscle endurance
  • Pressure biofeedback
  • Teachers
03

In context

Neck Pain

1,259 studies on the registry are indexed under Neck Pain; 256 are open to participants now.

This study's enrollment of 100 is above the median of 52 across 1,026 interventional studies indexed under Neck Pain.

Browse Neck Pain studies →

Lead sponsor

Riphah International University is the lead sponsor of 2,176 studies on the registry; 637 are open to participants now.

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

04

Who can participate

Ages eligible
24 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
100 participants (actual)

Study arms

  • Experimental
    Deep cervical muscle training using pressure biofeedback and conventional Exercises

    The duration of preesure biofeedback includes 3 sets in a session with 10 repetitions each with 2 minutes of rest between sets and 5 days a week for 6 weeks. Conventional exercises like Stretching and strengthening of neck flexor muscles will include 10 repetitions, each held for 10s with rest of 2 minutes between sets. The session will be conducted for 6 weeks, 5 days a week.

    Device: Pressure biofeedback

  • Experimental
    conventional exercises for Neck pain

    Only conventional exercises like stretching and strengthening of neck flexor muscles will be given.

    Other: Conventional exercises for deep cervical muscle training

Interventions

  • DevicePressure biofeedback

    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

06

What researchers measure

Primary outcomes

  1. Numeric pain rating Scale

    Numeric 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.

    Time frame: 8th week

  2. Inclinometer

    It is an instrument used for measuring the angles of tilt,elevation and depression of an object with respect to gravity.

    Time frame: 8th week

  3. Cranio-cervical flexion test

    It 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

    Time frame: 8th week

  4. Neck Disability index

    This questionnaire has been designed to give us information as to how your neck pain has affected your ability to manage in everyday life.

    Time frame: 8th week

07

Study locations

1 site
  • Riphah International University
    Faisalabad, Punjab Province 38000, Pakistan
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 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
NCT05261854
Responsible party
Sponsor
First posted
Mar 2, 2022
Start date
May 1, 2021
Primary completion
Mar 25, 2022
Completion
Apr 5, 2022
Last update
Jun 22, 2022

Study contacts

Muhammad Kashif
study chair · 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 Jun 2022. You cannot join it, but the record below documents what was studied.

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