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临床试验/NCT05064241
NCT05064241进行中(未招募)不适用

Investigations of Barriers and Methods to Overcome Barriers to Access Genetic Medicine

Boston Children's Hospital2 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2023年4月15日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
70
试验地点
2
主要终点
Qualitative self-report of referrals for clinical genetic services

研究概览

简要总结

To learn about patient barriers to accessing genetic medicine, we will analyze anonymous posts from a membership-based online community [Inspire.com], and investigate how these barriers differ for various populations. We will then test whether these barriers can be addressed by providing online access to a genetic counselor to answer patient questions for one group of patients (virtual advisory board group) and compare to that of a control group who does not have access to a genetic counselor (virtual peer-to-peer board group).

详细描述

Genomic medicine has the potential to advance diagnoses, predict risk, support prevention efforts, and inform treatment decision-making. Though technologies for measuring genetic variants have improved and become more cost-effective, clinical integration of genomic medicine has been surprisingly slow. For genomic medicine to be successfully implemented across specialties and across demographics, the systemic barriers that patients experience need to be identified and addressed.

Online health support is becoming an increasingly important part of healthcare as more patients use digital health networks. In the first part of this study, an analysis of online communication in a membership-based online support community [Inspire.com] will identify systemic, structural and individual barriers to accessing genomic medicine. A genetic counselor will be informed to these results and will be part of the intervention arm of the study.

To assess the extent to which online health networks can directly help genomic medicine implementation, participants will join one of two Virtual Discussion Boards (a Virtual Advisory Board and a Virtual Peer-to-Peer Discussion Board). In the intervention arm, the Virtual Advisory Board will have a genetic counselor answer patient questions online about genomic medicine once every week for a period of three months. In the control arm, participants will answer and comment on each others' questions in the Virtual Peer-to-Peer Discussion Board. We hypothesize that after six months, patients who participate in the Virtual Advisory Board are more likely to self-report receiving genomic medicine than those in the control arm. After completion of the study, participants in the Peer-to-Peer Discussion Board, we will give online access to the genetic counselor to answer any questions

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
Single (Participant)

盲法说明

Participants will not be told which discussion board they are randomized to. However, they may possibly discover that one board has a genetic counselor, and the other does not.

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

  • Member of Inspire.com Genetic disease Genetic predisposition to disease -

排除标准

  • Not member of Inspire.com No genetic disease No genetic predisposition to disease

结局指标

主要结局

Qualitative self-report of referrals for clinical genetic services

时间窗: 6 months

Percentage of participants with self-report of referrals for clinical genetic services

次要结局

  • Self-report of specific behaviors to overcome barriers to accessing genetic medicine(6 months)
  • Qualitative self-report of specific barriers to the participant accessing genomic medicine(6 months)

研究者

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

Catherine Brownstein

Assistant Professor

Boston Children's Hospital

研究点 (2)

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