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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01809457
Other study ID # S01 / UW 11-177
Secondary ID
Status Completed
Phase N/A
First received March 10, 2013
Last updated March 11, 2013
Start date March 2011
Est. completion date July 2012

Study information

Verified date March 2013
Source The University of Hong Kong
Contact n/a
Is FDA regulated No
Health authority Hong Kong: Department of Health
Study type Interventional

Clinical Trial Summary

to investigate the effectiveness of the educational poster regarding knowledge of dental trauma for the secondary school students


Description:

To investigate the effectiveness of the educational poster about dental trauma to increase the knowledge of secondary students.

Schools will be randomly divided into two groups, baseline score of knowledge in questionnaire will be collected for all subjects. Poster will be sent to intervention group, the school will place it at the notice broad or area of similar function in the classroom. For the control group, nothing will be given, then after 2 weeks, the score of knowledge by the second questionnaire of both groups will be collected again.

To compare the difference in knowledge before and after in both groups, statistical test will be performed.

Investigators conduct a cluster randomized controlled trial. A list of secondary schools was requested from the Education Bureau. Secondary schools will be invited to join the study and then randomized to the intervention group and the control group in the unit of school using computer generated numbers. All students will fill in the first questionnaire and send it back to the investigator in 1 week. Then copies of the same poster will be given to the intervention schools, these schools will be requested to place them in the classrooms of the participating students. No poster will be given to the control group. After 2 weeks, the poster will be removed. The same questionnaire will be filled out by all the students in both groups and sent back in 1 week. Then the data will be processed to show whether the poster is effective to improve the knowledge of the students.


Recruitment information / eligibility

Status Completed
Enrollment 671
Est. completion date July 2012
Est. primary completion date January 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 11 Years to 20 Years
Eligibility Inclusion Criteria

- All secondary schools in Hong Kong that the students can read Chinese or English

Exclusion Criteria

- no school consent or individual guardian consent

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Investigator, Outcomes Assessor)


Related Conditions & MeSH terms


Intervention

Other:
educational poster
educational poster for dental trauma

Locations

Country Name City State
Hong Kong secondary schools in Hong Kong Hong Kong

Sponsors (1)

Lead Sponsor Collaborator
The University of Hong Kong

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type Measure Description Time frame Safety issue
Primary knowledge score a questionnaire to test the knowledge score 2 weeks No
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