跳至主要内容
临床试验/NCT03213171
NCT03213171已完成不适用

Promoting Organ and Tissue Donation Registration in Family Physician Offices: a Pragmatic Stepped-wedge Cluster Randomized Controlled Registry Trial (RegisterNow Trial)

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's2 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2017年9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
6
试验地点
2
主要终点
Donor registration status at 7 days

研究概览

简要总结

This study evaluates the effects of using reception staff to prompt patients by providing a pamphlet and an opportunity to register in the waiting room via a mobile tablet on deceased organ donor registration rates.

详细描述

Background: There is a worldwide shortage of organs available for transplant, leading to preventable morbidity and mortality. While the majority of the general public in many countries support organ donation, actual donor registration rates are substantially out of step with these views. For instance, in Canada most Canadians support organ donation but less than 25% in most provinces have registered. The family physician office is a promising yet underused setting in which to address known barriers and facilitators to registration for deceased organ and tissue donation and to provide an immediate opportunity to register while in the waiting room for those wanting to do so.

Methods/Design: The investigators aim to evaluate the effects of having reception staff in family physician offices to prompt patients upon check-in with an educational pamphlet using a cluster, stepped-wedge randomized design. A mobile tablet will also be added to the waiting area to provide patients with the immediate opportunity to register. Family physicians are also provided with an educational booklet and encouraged to discuss organ donation with their patients. The investigators will use behaviour change techniques designed to address previously anticipated barriers and enablers to organ and tissue donation registration. The investigators will evaluate the effectiveness of the intervention conducted in six family physician offices in Ontario, Canada. Following a two-week baseline control period, offices will cross sequentially into the intervention arm in a random sequence at two-week intervals until all offices deliver the intervention (baseline + two weeks for each of six offices). The primary outcome will be the proportion of patients that have registered for deceased organ donation following in the 7 days following their office visit, using routinely collected registry data (i.e. administrative databases). The investigators will also conduct a qualitative post-trial process evaluation will assess reception staff and family physicians experiences with the intervention.

Discussion: Promoting organ and donor registration remains an important strategy for organ procurement organizations and patients worldwide. The results of this trial will inform a provincial roll-out strategy to promote organ donation in family physician offices.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Other
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
16 Years 至 105 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • for Patients
  • Inclusion Criteria:
  • Patients that visited a family physician
  • Patients that are at least 16 years of age with a valid health card (eligibility criteria to register for organ donation in Ontario)
  • Inclusion/Exclusion Criteria for Family Physicians (Cluster level)
  • Inclusion Criteria:
  • - Working at a site that sees at least 100 patients per week
  • Exclusion Criteria:
  • - Working at multiple sites that cannot be separated in analyses

研究组 & 干预措施

Usual care

No Intervention

Usual care / Standard of care No intervention implemented

Intervention

Experimental

Reception staff providing handout; Mobile tablet that provides the immediate opportunity for patients to register in the waiting room

干预措施: Reception staff providing handout. (Behavioral)

Intervention

Experimental

Reception staff providing handout; Mobile tablet that provides the immediate opportunity for patients to register in the waiting room

干预措施: Mobile Tablet (e.g. iPad) (Behavioral)

结局指标

主要结局

Donor registration status at 7 days

时间窗: 7 days

Donor registration status (Yes/ Not registered)

次要结局

  • Donor registration status at 30 days(30 days)
  • Donor registration status at 14 days(14 days)

研究者

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

Amit Garg

Professor

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

研究点 (2)

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