Effect Of Pressure Biofeedback on Deep Cervical Muscle Training Among University Teachers.
NCT ID: NCT05261854
Last Updated: 2022-06-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
100 participants
INTERVENTIONAL
2021-05-01
2022-04-05
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Cranio- Cervical Flexion Training With and Without Pressure Biofeedback in Mechanical Neck Pain
NCT04173143
Effects of Neck Stabilizers Retraining on Chronic Neck Pain
NCT07266610
Isometric Exercises With and Without Pressure Biofeedback in Computer Users With Cervical Spine Overload
NCT05026086
Comparative Effects of Visual and Pressure Biofeedback in Symptomatic Forward Head Posture.
NCT06151951
Integrated Neuromuscular Inhibition, Muscle Energy and Strain Counter Strain Techniques in Neck Pain
NCT05262062
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
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.
Pressure 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
conventional exercises for Neck pain
Only conventional exercises like stretching and strengthening of neck flexor muscles will be given.
Conventional exercises for deep cervical muscle training
Conventional exercise for deep cervical muscle training will be given 4 days a week for 6 weeks
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Pressure 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
Conventional exercises for deep cervical muscle training
Conventional exercise for deep cervical muscle training will be given 4 days a week for 6 weeks
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* 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.
24 Years
45 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Riphah International University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Muhammad Kashif
Role: STUDY_CHAIR
Riphah International University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Riphah International University
Faisalabad, Punjab Province, Pakistan
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
REC-FSD-00246
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.