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临床试验/NCT03958929
NCT03958929暂停不适用

A Randomized Controlled Trial on the Impact of an Educational Video on Satisfaction After Glaucoma Surgery in Urban and Rural China

Sun Yat-sen University1 个研究点 分布在 1 个国家目标入组 264 人开始时间: 2023年10月10日最近更新:
适应症

试验速览

阶段
不适用
状态
暂停
发起方
入组人数
264
试验地点
1
主要终点
The mean satisfaction outcome over two follow-up visits

研究概览

简要总结

Overall Objective: This study will assess whether an educational video is effective in increasing patient satisfaction with glaucoma surgery.

  1. Investigate the impact of educational interventions on glaucoma patients' surgical satisfaction.
  2. Investigate the post-operative satisfaction of rural glaucoma patients in county hospitals
  3. Investigate the difference in postoperative satisfaction between urban and rural glaucoma patients in urban hospitals
  4. Investigate other factors that influence postoperative glaucoma satisfaction.

详细描述

Glaucoma is the leading cause of irreversible blindness in China, as elsewhere in the world. In Chinese rural settings, where topical glaucoma medication is unlikely to be a practical and sustainable option, surgery is the primary treatment modality for glaucoma.

However, it is known that vision is quite likely to decline in the short to medium term after glaucoma surgery, and there are concerns that dis-satisfaction resulting from such vision changes might lead to negative social marketing, affecting uptake not only of glaucoma surgical care but other eye operations (principally cataract) as well. We propose to test the impact on post-operative satisfaction of a multi-media educational intervention designed to give patients a realistic expectation of their post operative course: glaucoma surgery is being performed NOT to improve vision, but do protect it from future harm, and vision may in fact decline for several weeks post operatively.

A randomized controlled design will be used, and subjects undergoing glaucoma surgery will be enrolled at 4 rural county hospitals in rural Guangdong province, and randomized to receive the intervention or usual care. The principal outcome will be subjective satisfaction on a previously-tested questionnaire instrument, administered pre-operatively and post-operatively on two occasions in the first month following surgery. Patients not returning post-operatively to the surgical facility will be contacted by telephone for administration of the questionnaire. Other facility- and patient-related clinical and personal factors expected to influence satisfaction will also be recorded, and adjusted for in all analyses.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

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

入选标准

  • age≥18 years, glaucoma patients who do the peripheral iridectomy or trabeculotomy

排除标准

  • patients who had been the trabeculotomy, vision≤0.05, severe psychotic disorders and dysgnosia

结局指标

主要结局

The mean satisfaction outcome over two follow-up visits

时间窗: 1 day, 1 week

The primary outcome is the mean satisfaction score calculated by adding up the satisfaction scores at two follow-up visits: 1 day and 1 week after surgery and dividing the total by the number of scores. The satisfaction score will be assessed as a cumulative score. Composite outcome, in which multiple end points are combined, are frequently used as primary outcome measures in randomized trials and are often associated with increased statistical efficiency, although such measure may prove challenging for the interpretation of results. (Freemantle N, Calvert M, Wood J, Eastaugh J, Griffin C. Composite outcomes in randomized trials: greater precision but with greater uncertainty? JAMA. 2003; 289: 2554-2559)

次要结局

  • Personality in both groups using Eysenck Personality Questionnaire-Revised Short Scale for Chinese (EPQ-RSC) access glaucoma patients personality(Baseline (before surgery))
  • Knowledge scores about glaucoma(Baseline (before surgery); 1 day and 1 week after surgery)
  • The rate of willingness to recommend surgery to a friend or relative with glaucoma(1 day, 1 week)
  • Intraocular pressure in both groups(Baseline (before surgery); 1 day and 1 week after surgery)
  • visual acuity in both groups(Baseline (before surgery); 1 day and 1 week after surgery)

研究者

发起方
Sun Yat-sen University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Congdon Nathan

Principal Investigator

Sun Yat-sen University

研究点 (1)

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