跳至主要内容
临床试验/NCT04902664
NCT04902664已完成不适用

A Multi-pronged Intervention to Initiate Shared Decision-making on Medical Tests and Care Cascades in the Primary Care Setting

Brigham and Women's Hospital1 个研究点 分布在 1 个国家目标入组 329 人开始时间: 2021年5月24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
329
试验地点
1
主要终点
Shared Decision-Making Process 4 Survey

研究概览

简要总结

The purpose of this randomized controlled trial is to evaluate the impact of patient and provider facing educational materials and peer comparison on medical testing conversations during annual physicals. The investigators hypothesize that education materials and peer comparison will improve conversation quality about medical testing decisions.

详细描述

Medical tests may show unexpected findings leading to additional tests, treatments, and visits that cost money and take time but may not have benefits. This is a prevalent issue with major consequences for patients and clinicians. Making informed decisions about when to order medical tests may help avoid unnecessary costs and worry. However, doctors don't always have detailed conversations about medical testing and there are patient gaps in knowledge. The investigators hypothesize that education materials and peer comparison to promote conversations about medical tests will improve conversation quality about medical testing decisions. The investigators have developed patient and provider-facing interventions to educate on and promote conversations about the uses and consequences of medical tests, and the investigators will test the impact of this just-in-time educational and peer comparison intervention on the likelihood of patients having productive conversations about medical tests. The effects of the intervention will be assessed using surveys before and after the study. This work has the potential to help patients feel more supported by their healthcare system, empower patients to participate in shared decision-making, and build trust between patients and clinicians.

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

  • (Physicians):
  • Primary care physicians at Brigham and Women's Hospital
  • In active practice
  • Inclusion criteria (Patients):
  • Adults age 18 years old or older
  • English-speaking
  • Access to email
  • Did not opt out of receiving research invitations from health system
  • Patients of participating physicians
  • Scheduled annual physical during the study period

排除标准

  • 未提供

研究组 & 干预措施

Intervention Arm

Experimental

Intervention arm physicians will receive an email with feedback on how they compare to their peers in aggregate on test ordering during annual physicals, along with physician-facing education materials. This email will be sent before each patient study visit for all patients in the study. Participating patients of intervention arm physicians will receive patient education materials one to two days before their study visit.

干预措施: Patient education materials (Behavioral)

Intervention Arm

Experimental

Intervention arm physicians will receive an email with feedback on how they compare to their peers in aggregate on test ordering during annual physicals, along with physician-facing education materials. This email will be sent before each patient study visit for all patients in the study. Participating patients of intervention arm physicians will receive patient education materials one to two days before their study visit.

干预措施: Physician peer-comparison email (Behavioral)

Intervention Arm

Experimental

Intervention arm physicians will receive an email with feedback on how they compare to their peers in aggregate on test ordering during annual physicals, along with physician-facing education materials. This email will be sent before each patient study visit for all patients in the study. Participating patients of intervention arm physicians will receive patient education materials one to two days before their study visit.

干预措施: Physician education materials (Behavioral)

Control Arm

Placebo Comparator

Control arm physicians receive an email with information on the general visit preparation tips that their patients will receive. Participating patients of control arm physicians will receive general visit preparation tips one to two days before their study visit.

干预措施: General visit preparation materials (Behavioral)

结局指标

主要结局

Shared Decision-Making Process 4 Survey

时间窗: Within two weeks after visit

Composite score of survey items completed by the patient after physician visit. Min 0, Max 4 (higher is better).

次要结局

  • Satisfaction with testing discussion(Within two weeks after visit)
  • Patient knowledge(Within two weeks after visit)
  • Presence of testing discussion(Within two weeks after visit)
  • Discussion of next steps(Within two weeks after visit)
  • Whether doctor explained tests in a way that was easy to understand(Within two weeks after visit)

研究者

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

Ishani Ganguli MD, MPH

Assistant Professor of Medicine

Brigham and Women's Hospital

研究点 (1)

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