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一项提高弱视高剂量遮盖治疗依从性的教育干预:一项随机对照试验。

An educational intervention to improve adherence to high-dosage patching regimen for amblyopia: a randomised controlled trial.

出版信息

Br J Ophthalmol. 2014 Jul;98(7):865-70. doi: 10.1136/bjophthalmol-2013-304187.

Abstract

BACKGROUND

Previous reports suggest that adherence to patching is a major issue in amblyopia treatment. We tested with an unmasked randomised controlled clinical trial whether an intense educational/motivational intervention improves adherence when a high-dose regime is prescribed.

METHODS

62 children with newly diagnosed amblyopia were randomly allocated into two treatment arms with and without educational/motivational intervention material. Both were prescribed patching 10 h/day, 6 days/week for a fixed period of 12 weeks. The intervention arm received an educational/motivational intervention before patching which included information booklets, video, a cartoon story book, sticker charts and a dedicated session with a researcher. The control arm received the usual clinical information. The primary outcome measure was adherence measured using electronic occlusion dose monitors where a success/failure binary outcome was used to account for participants who dropped out of the study defined as patching >4 h/day. Visual outcome, expressed as percentage visual deficit, was measured as secondary outcome.

RESULTS

The intervention increased adherence success rate from 45.2% in the control group to 80.6% in the intervention group (p=0.0027). However, visual outcome was not significantly better in the intervention group (p=0.190).

CONCLUSIONS

Our study shows that an intense educational/motivational intervention can improve adherence to patching to high prescribed doses although no significant improvement in visual outcome was observed. TRIALS REGISTRATION NUMBER: ISRCTN05346737 (International Standard Randomised Controlled Trial Number Register).

摘要

背景

先前的报告表明,在弱视治疗中,坚持遮盖是一个主要问题。我们通过一项非掩蔽随机对照临床试验来测试,当规定高剂量治疗方案时,强化教育/激励干预是否能提高依从性。

方法

62 名新诊断为弱视的儿童被随机分配到有和没有教育/激励干预材料的两个治疗组。两组均规定每天遮盖 10 小时,每周 6 天,持续 12 周。干预组在遮盖前接受教育/激励干预,包括信息手册、视频、卡通故事书、贴纸图表和与研究人员的专门会议。对照组接受常规临床信息。主要结局测量指标是使用电子眼罩剂量监测器测量的依从性,采用成功/失败的二分法来计算因未达到每天遮盖 4 小时以上而退出研究的参与者。视觉结果,以视觉缺陷百分比表示,作为次要结局进行测量。

结果

干预组的依从性成功率从对照组的 45.2%提高到干预组的 80.6%(p=0.0027)。然而,干预组的视觉结果并没有显著改善(p=0.190)。

结论

我们的研究表明,强化教育/激励干预可以提高对高规定剂量的遮盖依从性,尽管没有观察到视觉结果的显著改善。

试验注册号

ISRCTN05346737(国际标准随机对照试验注册号登记处)。

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