Effects of Deep Cervical Flexors Training On Forward Head Posture, Neck Pain and Functional Status
NCT ID: NCT04463199
Last Updated: 2020-07-13
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
30 participants
INTERVENTIONAL
2019-02-20
2019-09-02
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.
Stabilization vs Proprioception Training on Neck Flexor Endurance in Adolescents With Forward Head Posture
NCT07052149
Efficacy of Deep Cervical Training Combined With Mobilization Techniques on Forward Head Posture
NCT05650346
Postural Correction Exercises for Forward Head Posture
NCT03038139
Efficacy of Deep Cervical Flexor Muscles Training on Neck Pain, Functional Disability and Muscle Endurance in School Teachers
NCT03537300
Posture Correction Exercises for Forward Head Posture in Chronic Smartphone and Laptop Users
NCT06864780
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
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Experimental
Experimental group received craniocervical flexion training for 4 weeks and postural advice
Craniocervical flexion training
PBU airbag was clipped together and folded in, fastened, and placed suboccipital. Uninflated pressure sensor was kept below the neck, so that it touched the occiput then inflated to a stable baseline pressure of 20 mmHg to just fill the space below the neck but not to push it into lordosis. Subjects were demonstrated the correct action of the deep cervical flexors that is gentle nodding of head as if saying "yes".
Control Group
Control group received only postural advice
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Craniocervical flexion training
PBU airbag was clipped together and folded in, fastened, and placed suboccipital. Uninflated pressure sensor was kept below the neck, so that it touched the occiput then inflated to a stable baseline pressure of 20 mmHg to just fill the space below the neck but not to push it into lordosis. Subjects were demonstrated the correct action of the deep cervical flexors that is gentle nodding of head as if saying "yes".
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Neck disability index value less than 24 (mild to moderate disability scores on NDI)
* Forward head posture as identified by straight line down from external meatus falling anterior to shoulder and mid thorax.
* Using computer for at least 3 hours a day for at least 4 days a week or more.
Exclusion Criteria
* Ongoing or previous history of neurological signs
* Ongoing or previous history of inflammatory disease
* Ongoing or previous history of spinal tumor
* Ongoing or previous history of spinal infection
* Ongoing or previous history of spinal cord compression
* Ongoing or previous history of congenital, or acquired postural deformity
* Ongoing or previous history of cervical spinal surgery
* Ongoing or previous history of spinal instability
13 Years
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
King Saud University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Masood Khan
Principal investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
King Saud University
Riyadh, , Saudi Arabia
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.
RRC-2019-08
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.