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临床试验/NCT01499628
NCT01499628已完成不适用

Eccentric Fixation From Enhanced Clinical Training (EFFECT): A Randomised Clinical Trial for Patients With AMD

Moorfields Eye Hospital NHS Foundation Trust1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2011年4月27日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
200
试验地点
1
主要终点
Score on the Massof Activity Inventory - 6 month follow up

研究概览

简要总结

Age-related macular degeneration (AMD) is the leading cause of severe visual impairment in the UK, Europe and N America. Low vision patients with AMD have great difficulty reading, which leads to a loss of independence and reduced quality of life. Magnifiers alone do not compensate for loss of central vision in AMD. It has been proposed that special low vision training can improve reading ability in patients with AMD. Training programmes are widely available in the US and Scandinavia, but not in the UK, partly because there is a lack of evidence from Randomised Control Trials (RCT) showing that they are effective. The investigators are conducting a clinical trial comparing the conventional hospital-based low vision service to enhanced rehabilitation programmes that include Eccentric Viewing training. Eccentric viewing training involves teaching patients who have lost their central vision to use a new area of retina for visual tasks. Patients are either taught to improve the use of the part of the retina they naturally start using after their central vision is lost, their so-called preferred retinal locus (PRL), or, alternatively, they are taught to use a different retinal area that is thought to be better suited for everyday visual tasks, the so-called trained retinal locus (TRL). The investigators plan to compare the two types of eccentric viewing training to conventional hospital-based low vision care.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Diagnosis of age-related macular degeneration
  • •Visual acuity 6/12 to 3/60 inclusive in the better eye
  • •Dense central scotoma confirmed by microperimetry

排除标准

  • •Patients who are not fluent in English or are cognitively impaired
  • •Patients with serious hearing impairment
  • •Patients who are hospital inpatients, who are living in nursing homes or are otherwise non-independent
  • •Ocular co-morbidity (other than mild cataract) in the better eye
  • •Recent low vision assessment or eccentric viewing training

研究组 & 干预措施

Group 4-EVT at the TRL

Experimental

Eccentric viewing training at the Trained Retinal Locus (TRL), using reading/target cards and microperimeter. Three 45 minute sessions completed over three weeks.

干预措施: EVT at the TRL (Behavioral)

Group 1-Control

No Intervention

No extra training will be given.

Group 2-Control plus supervised reading

Active Comparator

The same amount of contact time as Groups 3 and 4 - three 45 minute sessions completed over three weeks.

干预措施: Supervised Reading (Behavioral)

Group 3-EVT at the PRL

Experimental

Eccentric viewing training at the Preferred Retinal Locus (PRL), using reading/target cards. Three 45 minute sessions completed over three weeks.

干预措施: EVT at the PRL (Behavioral)

结局指标

主要结局

Score on the Massof Activity Inventory - 6 month follow up

时间窗: Change from Baseline in Massof Activity Inventory at 6 month follow up

次要结局

  • Quality of Life (MacDQoL) - Final Assessment(Change from Baseline in Quality of Life (MacDQoL) at Final Assessment)
  • WHO (Five) Well-Being Index (WBI-5) - 12 month follow up(Change from Baseline in WBI-5 score at 12 month follow up)
  • Reading Speed (ReST) - Final Assessment(Change from Baseline in Reading Speed (ReST) at Final Assessment)
  • Quality of Life (MacDQoL) - 6 month follow up(Change from Baseline in Quality of Life (MacDQoL) at 6 month follow up)
  • Self-reported health status (EQ-5D) - 6 month follow up(Change from Baseline in EQ-5D score at 6 month follow up)
  • Self-reported health status (EQ-5D) - 12 month follow up(Change from Baseline in EQ-5D score at 12 month follow up)
  • WHO (Five) Well-Being Index (WBI-5) - Final Assessment(Change from Baseline in WBI-5 score at Final Assessment)
  • WHO (Five) Well-Being Index (WBI-5) - 6 month follow up(Change from Baseline in WBI-5 score at 6 month follow up)
  • Interpersonal Support Evaluation List (ISEL) - 6 month follow up(Change from Baseline in Interpersonal Support Evaluation List (ISEL) at 6 month follow up)
  • Acceptance and Self Worth Adjustment Scale (AS-WAS) - 12 month follow up(Change from Baseline in Acceptance and Self Worth Adjustment Scale (AS-WAS) at 12 month follow up)
  • Massof Activity Inventory - Final Assessment(Change from Baseline in Massof Activity Inventory at Final Assessment)
  • Quality of Life (MacDQoL) - 12 month follow up(Change from Baseline in Quality of Life (MacDQol) at 12 month follow up)
  • Self-reported health status (EQ-5D) - Final Assessment(Change from Baseline in EQ-5D score at Final Assessment)
  • Time Trade Off (TTO) - 6 month follow up(Change from Baseline in Time Trade Off (TTO) score at 6 month follow up)
  • Interpersonal Support Evaluation List (ISEL) - Final Assessment(Change from Baseline in Interpersonal Support Evaluation List (ISEL) at Final Assessment)
  • Acceptance and Self Worth Adjustment Scale (AS-WAS) - Final Assessment(Change from Baseline in Acceptance and Self Worth Adjustment Scale (AS-WAS) at Final Assessment)
  • Acceptance and Self Worth Adjustment Scale (AS-WAS) - 6 month follow up(Change from Baseline in Acceptance and Self Worth Adjustment Scale (AS-WAS) at 6 month follow up)
  • Interpersonal Support Evaluation List (ISEL) - 12 month follow up(Change from Baseline in Interpersonal Support Evaluation List (ISEL) at 12 month follow up)
  • Massof Activity Inventory - 12 month follow up(Change from Baseline in Massof Activity Inventory at 12 month follow up)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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