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British Journal of Ophthalmology 2002;86:915-919; doi:10.1136/bjo.86.8.915
Copyright © 2002 by the BMJ Publishing Group Ltd.
British Journal of Ophthalmology 2002;86:915-919
© 2002 British Journal of Ophthalmology

CLINICAL SCIENCE

Design of the Monitored Occlusion Treatment of Amblyopia Study (MOTAS)

C E Stewart1, A R Fielder1, D A Stephens2 and M J Moseley1

1 Department of Ophthalmology, Imperial College of Science, Technology and Medicine, London, UK
2 Department of Mathematics, Imperial College of Science, Technology and Medicine, London, UK

Correspondence to:
Correspondence to:
Catherine E Stewart, Department of Ophthalmology, Imperial College of Science, Technology and Medicine, Western Eye Hospital, 171 Marylebone Road, London NW1 5QH, UK

Background/aims: The effectiveness of occlusion therapy for the treatment of amblyopia is a research priority. The authors describe the design of the Monitored Occlusion Treatment for Amblyopia Study (MOTAS) and its methodology. MOTAS will determine the dose-response relation for occlusion therapy as a function of age and category of amblyopia.

Methods: Subjects progress through up to three study phases: (1) Assessment and baseline phase: On confirmation of eligibility, and after parental consent, baseline visual functions are determined, and spectacles prescribed as necessary; (2) Refractive adaptation phase: Subjects wear spectacles full time and return to clinic at 6 weekly intervals until 18 weeks, by which time all improvement due to refractive correction is complete; (3) Occlusion phase: All subjects are prescribed 6 hours of occlusion per day. Daily occlusion is objectively monitored using an occlusion dose monitor (ODM). Outcome variables: visual acuity (logMAR charts), log contrast sensitivity (Pelli-Robson chart), and stereoacuity (Frisby) are assessed at 2 weekly intervals until gains in visual acuity cease to be statistically verifiable.

Conclusion: Four methodological issues have been addressed; firstly, baseline stability of visual function; secondly, differentiation of refractive adaptation from occlusion; thirdly, objective measurement of occlusion dose and concordance; fourthly, use of validated outcome measures.

Keywords: amblyopia; occlusion therapy; occlusion dose monitor; refractive adaptation; dose-response


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  • Mitchell, D. E, Sengpiel, F. (2009). Neural mechanisms of recovery following early visual deprivation. Phil Trans R Soc B 364: 383-398 [Abstract] [Full Text]  
  • Stewart, C. E, Stephens, D. A, Fielder, A. R, Moseley, M. J, ROTAS Cooperative, (2007). Objectively monitored patching regimens for treatment of amblyopia: randomised trial. BMJ 335: 707-707 [Abstract] [Full Text]  
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  • Sankari, P R, Henshall, V, O'Regan, K, Cobb, C J, Russell, K, Cox, A, MacEwen, C J (2003). "Compliance" with treatment in amblyopia is an important factor affecting the final visual outcome. Br. J. Ophthalmol. 87: 928-928 [Full Text]  
  • Fleck, B W (2003). Amblyopia therapy. Br. J. Ophthalmol. 87: 255-256 [Full Text]  

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