Actively Recruiting
Pilot Study of Normative Range of Field of Binocular Single Vision in Adults in Singapore
Led by Tan Tock Seng Hospital · Updated on 2026-01-09
30
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The assessment and monitoring of the field of binocular single vision remains a crucial aspect of ophthalmological care, yet current clinical practice relies on normative standards established by Feibel \& Roper-Hall in 1974 that present significant limitations for contemporary application. The original study, conducted with a demographically homogeneous Caucasian population in St Louis using only "several" normal individuals, raises concerns regarding its applicability to Asian populations, particularly in Singapore, where ethnic and genetic factors may influence ocular characteristics. The limited sample size significantly increases the likelihood of Type II errors, whilst the temporal gap of over five decades introduces additional concerns regarding population changes, environmental factors, and advances in measurement techniques that have not been incorporated into current normative data. Given these substantial limitations in demographic representation, statistical power, and temporal relevance, there exists a pressing need to establish population-specific normative data for the field of binocular single vision in Singapore's adult population, which would provide more clinically relevant reference values and potentially improve diagnostic accuracy for ocular conditions in the local context.
CONDITIONS
Official Title
Pilot Study of Normative Range of Field of Binocular Single Vision in Adults in Singapore
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 21 and 59 years old
- Male or female gender
- Asian descent
- Able to understand spoken instructions in British/American English, Mandarin Chinese, or Bahasa Melayu
- Able to comply with the study protocol as judged by the investigator
- Able to understand and provide signed informed consent before any study assessments
You will not qualify if you...
- Unable to understand spoken instructions
- History of any facial, ocular, or head trauma
- History of any ocular disease or ocular surgery
- Presence of systemic medical conditions
- Near visual acuity worse than N6 at 40 cm in either eye, monocularly or binocularly without aid
- Ocular alignment of 10 prism diopters or more at near in primary, right, left, up, or down gaze
- Extraocular movement over-action or under-action of 0.5 or greater in any cardinal gaze
- Abnormal monocular visual field on confrontational test
- Abnormal or asymmetric extraocular muscle action pattern on Hess chart test
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Tan Tock Seng Hospital
Singapore, Singapore, Singapore, 308433
Actively Recruiting
Research Team
Z
Zheng Kuang Noel Soh, BSc
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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