Dichoptic training

二联训练
  • 文章类型: Clinical Trial Protocol
    背景:开发治疗弱视的替代方法的兴趣长期以来一直是临床医生和研究人员感兴趣的话题,因为规定的封堵和惩罚疗法并不总是提供有效的反应,并且与复发和不依从性的高风险相关.这里,我们提出了一种小规模RCT方案,以评估一种新型的基于VR的系统的安全性和临床疗效,该系统旨在为屈光参差性弱视儿童提供双眼视觉训练.
    方法:我们的目标是从巴利亚多利德大学临床医院和阿利坎特维萨斯·梅迪玛国际医院的儿科眼科病房招募60名年龄为5-17岁的屈光参差性弱视儿童。符合资格标准并同意参加的儿童将被随机分配到为期三个月的干预组,使用NEIVATECH系统进行18个半小时的办公室治疗(A组),或接受2小时的常规治疗的平行组每天在家中进行相同的时间(B组)。视觉功能评估将在干预前和1、2和3个月进行,距离BCVA的变化是需要考虑的主要结果指标。患者安全,合规,对治疗的满意度和接受度也将在治疗后作为其他有价值的结局指标进行评估.此外,将在干预前访视和干预后访视时对每组5名患者的亚组进行rsfMRI扫描,以测试两种疗法对视皮层神经可塑性的影响.
    结论:NEIVATECH系统被认为是一种严肃的游戏,旨在通过补充感知学习的概念,为屈光参差弱视儿童提供双眼视觉训练,在沉浸式VR环境中进行双重训练和游戏化。我们希望这种新颖的方法可以比迄今为止通过常规的屈光参差性弱视儿童修补方法提供的视力性能有更大的改善。
    背景:该协议于2021年3月29日在ClinicalTrials.gov(NCT04819386)注册。
    BACKGROUND: Interest in developing alternative methods for the treatment of amblyopia has long been a topic of interest among clinicians and researchers, as prescribed occlusion and penalization therapies do not always provide an effective response and are associated with a high risk of recurrence and non-compliance. Here, we present the protocol of a small-scale RCT to evaluate the safety and clinical efficacy of a novel VR-based system designed to provide binocular vision training to children with anisometropic amblyopia.
    METHODS: We aim to recruit a total of 60 children with anisometropic amblyopia aged 5-17 years with no previous treatment for amblyopia other than refractive correction from the pediatric ophthalmology units of the University Clinical Hospital of Valladolid and the Vithas Medimar International Hospital of Alicante. Children who meet the eligibility criteria and consent to participate will be randomly assigned to a three-month intervention group of 18 half-hour in-office therapy sessions with the NEIVATECH system (group A) or to a parallel group receiving 2 hours of conventional patching per day at home for the same period of time (group B). Assessments of visual function will be carried out before the intervention and at 1, 2 and 3 months, with changes in distance BCVA being the primary outcome measure to be considered. Patient safety, compliance, satisfaction and acceptance to treatment will also be assessed after therapy as other valuable outcome measures. In addition, a rsfMRI scan will be performed on a subgroup of 5 patients from each group at the pre-intervention visit and at the post-intervention visit to test the effects of both therapies on neural plasticity in the visual cortex.
    CONCLUSIONS: The NEIVATECH system has been conceived as a serious game designed to provide binocular vision training to anisometropic amblyopic children by complementing the concepts of perceptual learning, dichoptic training and gamification in an immersive VR environment. We hope that this novel approach may lead to greater improvements in vision performance than those provided so far by conventional patching in anisometropic amblyopic children.
    BACKGROUND: This protocol was registered with ClinicalTrials.gov ( NCT04819386 ) on 29 March 2021.
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  • 文章类型: Journal Article
    背景:在这项研究中,我们的目的是确定我们的视力治疗计划对7至10岁表现出对常规治疗不再有反应的双侧弱视患者的效果。
    方法:对2016年至2019年在中国医科大学附属医院接受视力治疗的7~10岁双侧弱视儿童进行回顾性分析。年龄和视力匹配的双侧弱视者作为对照组。通过兼职修补和完全屈光矫正,两组的视力在3个月以上均无改善。最初和最终的视力,立体视觉,和屈光状态进行了分析。
    结果:这里,治疗组15例,对照组16例。在端点,研究组显示出BCVA的显着改善,对照组的平均logMAR为0.32±0.15(3行改善),而logMAR为0.003±0.19(几乎没有改善)(p<0.001)。治疗的益处在治疗后的前3个月最明显(p<0.001),并持续到终点。立体灵敏度也从190.00±163.34提高到85.00±61.24弧秒,提高了55.26%。
    结论:视觉疗法,包括矫正治疗,知觉学习和二叉训练,是一项成功的计划,可以提高对常规治疗无反应的7至10岁双侧弱视儿童的视力和立体敏锐度。
    BACKGROUND: In this study we aim to determines the effect of our vision therapy program for 7- to 10-year-old patients who exhibit bilateral amblyopia that is no longer responsive to conventional treatment.
    METHODS: Children with bilateral amblyopia between the ages of 7 and 10 treated with vision therapy at the China Medical University Hospital between 2016 and 2019 were retrospectively reviewed. Age and visual acuity-matched bilateral amblyopes are included as a control group. The visual acuity for both groups showed no improvement for more than 3 months with part-time patching and full refraction correction. The initial and final visual acuity, stereopsis, and refractive status were analyzed.
    RESULTS: Here, 15 cases were included as the treatment group and 16 cases as a control group. At the endpoint, the study group shows a significant improvement in BCVA, with a mean of 0.32 ± 0.15 logMAR (3 lines improvement) versus 0.003 ± 0.19 logMAR (nearly no improvement) for the control group (p < 0.001). The benefits of treatment are most obvious in the first 3 months after treatment (p < 0.001) and last until the end point. Stereoacuity also improves from 190.00 ± 163.34 to 85.00 ± 61.24 arc seconds, which is a 55.26% improvement.
    CONCLUSIONS: Vision therapy, comprising orthoptic therapy, perceptual learning and dichoptic training, is a successful program for increasing visual acuity and stereoacuity in 7- to 10-year-old children with bilateral amblyopia that is unresponsive to conventional treatment.
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