- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03129958
Correlation Between Neck Pain and Postural Abnormalities Among Female Office Workers at University of Dammam
This study is a cross sectional study conducted to find out the Correlation between neck pain and postural abnormalities among female office workers at University of Dammam by objective assessments methods.
Eligible participants will sign the consent form followed by filling up demographic data, visual analog scale & neck disability index.
After that, Forward Head posture and Thoracic Kyphosis posture will take place by valid and reliable methods.
Study Overview
Status
Conditions
Detailed Description
The study population and sampling were calculated by Raosoft sample size calculator using an estimated average of population size 200 and allowing a 5% tolerable error, based on a 95% confidence interval (CI).
About 140 female office workers were targeted from the medical colleges of University of Dammam (UoD); Medicine, Applied Medical Science, Nursing, Dentistry, Clinical Pharmacology and Health Track of preparatory year were recruited into the study (N=140).
The study was approved by the Institutional Review Board (IRB) at the University of Dammam (IRB-PGS-2015-03-194).
Eligible individuals for this study were informed of the risks and benefits and were asked to read and sign a written consent form.
Participants' confidentiality was maintained by using a code (number) instead of the participant's name on the data collection form.
All data collection forms were saved in a file and secured in a locker & the electronic file saved with password. Only the researcher and the supervisor had an access to them.
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Subjects with/without non-specific neck pain complaint.
- Age from 28 up to 40 years old.
- At least 25 working hours a week ( at least 2 hours on computer - at least 3 other office working).
- More than 5 years of experience as an office worker.
Exclusion Criteria:
- Subjects who had prolonged absence from work anticipated within the past 12 months.
- Complain of: cervical radiculopathy, migraine, vestibular Dysfunction.
- Had spinal fracture or surgery.
- Pregnancy.
- History of cervical trauma.
- Comorbid medical conditions as cancer, type 1 diabetes, heart disease.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
pain
Time Frame: 2 min
|
by VAS
|
2 min
|
Disability
Time Frame: 5 min
|
by Neck Disability Index
|
5 min
|
Forward head posture
Time Frame: 10 min
|
by Myrin's Inclometer/ Goniometer
|
10 min
|
Thoracic kyphosis
Time Frame: 10 min
|
by spinal mouse
|
10 min
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: DOAA A AL-SALEH, bachelor, Imam Abdulrahman Bin Faisal University
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Doaa
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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