- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04582851
Prevalence of Temporomandibular Joint Disorders Among Egyptian University Postgraduate Students
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Matching criteria and allocation ratio The planned study a single arm cross sectional study, in which the prevalence of students of TMD will be reported. The association between TMD and other variables will be also studied. Gender, Age, Psychological stress, non-nutritional oral habits as nail biting, lip biting, object biting and grinding of teeth (bruxism & clenching), Para-functional habits, such as intensive gum chewing, leaning of the chin on the hand and mouth breathing , previous dental treatment and previous jaw trauma will be all studied.
Data sources and management Data sources, the answered questionnaires and subsequent spread sheets will only be shared by the team members.
ddressing potential sources of bias Selection bias: Sampling will be convenient sampling, Questionnaires will be handed to the students, otherwise an email will be sent to all the students through their university email addresses if COVID-19 situation prevails.
Statistical methods Statistical methods
All confounders, effect modifiers and exposures will be controlled for by crude and adjusted regression analyses, where the primary analysis will be the adjusted one. Failure to do so as a result of violating principles of a regression model will call for a subgroup analysis, where a student t test will be used for the comparison between the subgroups.
It is also planned to study the interactions between the variables via ANOVA test if the data show normal distribution.
Participants with missing data will be excluded.
- Cross-sectional study-Since the planned sampling method is cluster sampling, where the design effect factor becomes greater than 1.
Sensitivity of the results to adjusted and crude analysis will be done.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Maram Taema, masters
- Phone Number: 01005487077
- Email: maram.taema@dentistry.cu.edu.eg
Study Contact Backup
- Name: Iman Radi, masters
- Phone Number: 01001539613
- Email: iman.abdelwahab@dentistry.cu.edu.eg
Study Locations
-
-
-
Cairo, Egypt, 11518
- Recruiting
- Cairo University
-
Contact:
- Ahmad Diab
-
Sub-Investigator:
- Mohamed Khashab, PhD
-
Principal Investigator:
- Ahmad Diab
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Postgraduate students in Egyptian universities
- Age ranges from 18-45 years
- Males and females
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Postgraduate students
prevalence of TMD among postgraduate students.
|
exposure factors causing TMD
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
prevalence of TMDs in Egyptian university students
Time Frame: 3 months
|
by fonseca questionnaire
|
3 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ahmed Diab, BDS, Cairo University
- Study Chair: Essam Aziz, Phd, Cairo University
- Study Director: Maram Taema, Masters, Cairo University
- Principal Investigator: mohamed khashab, phd, Cairo University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 9102020
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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