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
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COMPLETED
NA
133 participants
INTERVENTIONAL
2023-03-08
2024-03-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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The conventional oral education group
Patients were only orally educated about glaucoma, preoperative preparation, surgical procedures, anaesthesia methods, and precautions during the preoperative visit.
No interventions assigned to this group
The Visual aids plus conventional oral education group
Patients were orally educated about glaucoma, preoperative preparation, surgical procedures, anaesthesia methods, and precautions with pictures and videos during the preoperative visit.
Visual aids
Diagrams, models, and videos
Interventions
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Visual aids
Diagrams, models, and videos
Eligibility Criteria
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Inclusion Criteria
* Illiterate or with ≤ 9 years of compulsory education
* Indications for filtering surgery
Exclusion Criteria
* Cognitive impairment
18 Years
ALL
No
Sponsors
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Shantou University Medical College
OTHER
Joint Shantou International Eye Center of Shantou University and the Chinese University of Hong Kong
OTHER
Responsible Party
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Laiwen Lv
Mr.
Principal Investigators
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Chukai Huang, PhD
Role: STUDY_DIRECTOR
Joint Shantou International Eye Center of Shantou University and the Chinese University of Hong Kong
Locations
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Joint Shantou International Eye Center of Shantou University and the Chinese University of Hong Kong
Shantou, Guangdong, China
Countries
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Other Identifiers
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EC 20220505(4)-P30
Identifier Type: -
Identifier Source: org_study_id
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