- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05261854
Effect Of Pressure Biofeedback on Deep Cervical Muscle Training Among University Teachers.
June 20, 2022 updated by: Riphah International University
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
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
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.
Study Type
Interventional
Enrollment (Actual)
100
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
-
-
Punjab
-
Faisalabad, Punjab, Pakistan, 38000
- Riphah International University
-
-
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
24 years to 45 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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.
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 |
|---|---|
|
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. |
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
|
|
Experimental: conventional exercises for Neck pain
Only conventional exercises like stretching and strengthening of neck flexor muscles will be given.
|
Conventional exercise for deep cervical muscle training will be given 4 days a week for 6 weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numeric pain rating Scale
Time Frame: 8th week
|
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.
|
8th week
|
|
Inclinometer
Time Frame: 8th week
|
It is an instrument used for measuring the angles of tilt,elevation and depression of an object with respect to gravity.
|
8th week
|
|
Cranio-cervical flexion test
Time Frame: 8th week
|
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
|
8th week
|
|
Neck Disability index
Time Frame: 8th week
|
This questionnaire has been designed to give us information as to how your neck pain has affected your ability to manage in everyday life.
|
8th week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 1, 2021
Primary Completion (Actual)
March 25, 2022
Study Completion (Actual)
April 5, 2022
Study Registration Dates
First Submitted
February 20, 2022
First Submitted That Met QC Criteria
February 20, 2022
First Posted (Actual)
March 2, 2022
Study Record Updates
Last Update Posted (Actual)
June 22, 2022
Last Update Submitted That Met QC Criteria
June 20, 2022
Last Verified
June 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC-FSD-00246
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
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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