Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-25 @ 12:01 AM
Ignite Modification Date:
2025-12-25 @ 12:01 AM
NCT ID:
NCT03129958
Brief Summary:
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.
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:
NCT03129958
Study Brief:
Protocol Section:
NCT03129958