跳至主要内容
临床试验/NCT06000865
NCT06000865招募中不适用

The GRADE Randomized Trial: Glaucoma Rehabilitation With Action viDeo Games and Exercise

The Hong Kong Polytechnic University2 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2023年9月9日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
56
试验地点
2
主要终点
Gait Measure - Time Up and Go test combining Narrow path walking test

研究概览

简要总结

Falls are one of the most serious public health concerns for seniors, with significant medical and economic consequences. This concern is even higher in patients with peripheral field loss due to glaucoma because of the patients' compromised visual input. The investigators' project proposes an innovative, entertaining, easily accessible and enjoyable intervention for improving mobility and postural control function in glaucoma patients with peripheral vision loss, who are more prone to falls and suffer from fear of falling. The new intervention examined in this project can be implemented in current vision and balance rehabilitation programs, and may benefit patients with different types of visual impairment to minimize their risk of falls and improve their quality of life.

详细描述

A prospective, 2-arm, randomized, single-blind, active-control trial will enroll 56 moderately- to severely-affected glaucoma patients with stable peripheral field loss, intact cognitive function, and no history of balance training. Participants will be randomly assigned 1:1 to one of two groups: 1) standing, physically interactive action video-game training (AVG_PI); and 2) conventional physical training (PT). AVG using a Nintendo Switch gaming station will be administered in 20 sessions over 10 weeks (45 minutes per session, 2 sessions per week). Participants in the AVG_PI will be in standing position with game controllers or sensors attached to the body while playing games involving muscle stretching and strengthening exercises. Participants in the PT will receive 45-minutes conventional physical training. Outcome measures will be assessed before training, and after 10 and 20 training sessions. The primary outcome measure is a test of mobility, and the secondary outcome measures include tests for dynamic balance plus visual cognition, static balance, visual cognition, and patient reported outcomes for fear of falling and quality of life.

研究设计

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

入排标准

年龄范围
55 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Presence of moderate to severe bilateral glaucomatous optic neuropathy (GON) from primary open-angle (including normal tension) or angle-closure glaucoma, as determined by an ophthalmologist, with abnormal Glaucoma Hemifield Test on standard Humphrey Field Analyzer 24-2 testing and matching nerve-fiber layer thinning on optical coherence tomography;
  • Stable vision and visual field loss for at least 3 months;
  • With a best-corrected distance acuity of 6/12 or better (equivalent to 0.3 logMAR acuity or better to confirm that participant's central vision is preserved);
  • With a cognitive functional score of 22 or above in the Montreal Cognitive Assessment - Hong Kong version (to confirm participants' intact cognitive function).

排除标准

  • Advanced glaucoma with GON of median deviation worse than -25 decibel;
  • Ocular diseases other than glaucoma (e.g., age-related macular degeneration, diabetic retinopathy, and moderate to severe cataract);
  • Severe medical problems (e.g., stroke, Parkinson's disease) or self-reported neurological (e.g. brain surgery, brain tumor and peripheral neuropathy), or cognitive disorders (e.g., diagnosed dementia or cognitive impairment);
  • Physical impairments (e.g. need the use of orthopedic and mobility aids) or physical limitations restricting them from independent walking;
  • Self-reported or medically diagnosed vestibular/ cerebellar dysfunction, history of vertigo, or severe hearing loss;
  • Using any medications for any neurological conditions or psychiatric drugs (e.g. sedative, hypnotic) that might interfere motor control; and
  • Currently attending any intensive physical/balance training.

结局指标

主要结局

Gait Measure - Time Up and Go test combining Narrow path walking test

时间窗: Change from baseline at week 5 and change from baseline at week 10.

Time Up and Go test combining Narrow path walking test: All participants need to stand up from a 46 cm height chair, walk on the path at their usual pace until the strip of a non-reflective tape, cross over the tape, turn 180°, walk to the starting position and finally sit down. Then repeat the same procedure within a narrower width. Participants need to use the dominant leg to step onto the standing position on one force plate while the non-dominant leg stands on the other force plate. The test will repeat for 10 times. Participants' gait parameters including hip flexion/extension (degree), knee Min/Max (degree), ankle flexion/extension (degree), walking speed (mm/s), step width (mm), and step length(mm) will be measured and analyzed for each condition.

次要结局

  • Quality of Life Questionnaire measure(Change from baseline at week 5 and change from baseline at week 10.)
  • Reaction time (RT)(Change from baseline at week 5 and change from baseline at week 10.)
  • Cognitive Reflection Test(Change from baseline at week 5 and change from baseline at week 10.)
  • Static Balance Measure(Change from baseline at week 5 and change from baseline at week 10.)
  • Perturbed Balance Measure(Change from baseline at week 5 and change from baseline at week 10.)
  • Useful field of view (UFOV)(Change from baseline at week 5 and change from baseline at week 10.)
  • Fear of Falling Questionnaire measure(Change from baseline at week 5 and change from baseline at week 10.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Allen MY Cheong

Professor

The Hong Kong Polytechnic University

研究点 (2)

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