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临床试验/NCT03874195
NCT03874195已完成不适用

Usability Testing of a Web-based Tool to Prepare Patients for Palliative Care

Duke University2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2017年1月11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
发起方
入组人数
80
试验地点
2
主要终点
System usability as measured by the system usability scale

研究概览

简要总结

The purpose of this study is to test the usability of PCforMe, a web-based preparation and engagement tool about palliative care, during a pre-visit pilot trial in outpatient palliative care at the Duke Cancer Institute Palliative Care Clinic.

详细描述

The Investigator will 1:1 randomize patients to an Active Control arm or Intervention arm. Both arms will receive a tablet computer (iPad or Galaxy Tab based on preference) connected to the internet with disposable headphones to use for up to 30 minutes. Subjects in the Active Control arm will receive a list of three nationally-recognized websites to receive information on palliative care - www.palliativedoctors.org; getpalliativecare.org; and Wikipedia "Palliative Care" https://en.wikipedia.org/wiki/Palliative_care). Intervention Arm subjects will receive access to PCforMe.

PCforMe is an online, web-based, interactive tool to prepare patients for a clinical palliative care encounter. PCforMe is accessible through www.pcforme.org. It does not collect any patient information, including identifiers (e.g. name, email address, disease, location) or health information (e.g. disease, symptom severity or location). The system uses a combination of animated videos and user-answered questions to generate a "Palliative Care Passport", which is a summary of information entered into the system. Research staff will print out the Passport for patients and hand it to them prior to the appointment.

Queries for users include standard-of-care questions asked by palliative care clinicians, including areas that patients want to more learn about. No diagnoses, medication advice, or clinical assessments are made or given.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
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

  • Potential participants will be identified by reviewing clinic appointment listings in EPIC (e.g., diagnosis, date of diagnosis, date of clinic appointment, physician), and deemed eligible by the RA by meeting the following criteria:
  • capacity to give consent
  • has a scheduled outpatient visit (initial consult) with a palliative care provider
  • ability to speak and understand English

排除标准

  • Not meeting the inclusion requirements

研究组 & 干预措施

Control

Active Comparator

Subjects in the Active Control arm will receive a list of three nationally-recognized websites to receive information on palliative care - www.palliativedoctors.org; getpalliativecare.org; and Wikipedia "Palliative Care" https://en.wikipedia.org/wiki/Palliative care).

干预措施: Access to three nationally-recognized Palliative Care websites for review (Behavioral)

Intervention

Experimental

Intervention Arm subjects will receive access to PCforMe.

干预措施: Access to PCforMe for review (Behavioral)

结局指标

主要结局

System usability as measured by the system usability scale

时间窗: 1 hour

To determine usability, the System Usability Scale will be administered to each participate. As described by usability.gov: "The participant's scores for each question are converted to a new number, added together and then multiplied by 2.5 to convert the original scores of 0-40 to 0-100. Though the scores are 0-100, these are not percentages and should be considered only in terms of their percentile ranking. Based on research, a SUS score above a 68 would be considered above average and anything below 68 is below average, however the best way to interpret the participant's results involves "normalizing" the scores to produce a percentile ranking." The original scale is a 10-item, 5-point Likert scale.

次要结局

  • Change in single-item Prepared item(Baseline, up to 1 hour)
  • Change in Palliative Care knowledge(Baseline, up to 1 hour)
  • Change in Perceived Efficacy for the Patient-Physician Interaction (PEPPI)(Baseline, up to 1 hour)

研究者

发起方
Duke University
申办方类型
Other
责任方
Sponsor

研究点 (2)

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