跳至主要内容
临床试验/NCT06078137
NCT06078137已完成不适用

Impact of an Enhanced Patient Reported Outcome Measurement (PROM) Strategy on PROM Completion Rates, Decision Support, and Patient Experience: A Hybrid Effectiveness-Implementation Study

University of Texas at Austin2 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2023年9月1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
200
试验地点
2
主要终点
Completion of deprioritization options 1 or 2 at 6-week follow-up via text or email

研究概览

简要总结

in clinical practice has been curbed by issues related to the variability in use of these tools for decision-making, and universally poor completion rates over time. Patients may not see the relevance of responding to questions about their health, and the results may not be reviewed by the clinician or presented and visualized with the patient. The questions may seem impersonal (e.g. too general and not directly assessing their individual goals, motivations, aspirations), irrelevant (e.g., asking about symptoms of depression when a person is seeking musculoskeletal specialty care) and insensitive (e.g., asking about sensitive subjects at the outset thereby disengaging the individual), and redundant or awkward (e.g., presenting questions that seem very similar or administered in strange orders). Finally, PROMs may also confer some burden (e.g., long PROM questionnaires often used for research may be unnecessarily burdensome for patient care), and provide logistical challenges (e.g., difficulties in administering the tools at the right time points), adding to a poor patient experience.

详细描述

The investigator sought to assess the impact of an enhanced and more personalized PROM strategy to overcome these barriers by providing i) a primer ahead of PROMs administration, ii) simple 3-part survey capturing capability, comfort, and calm, iii) a short distress and misconception survey, iv) goal setting question, v) summary sheet of PRO scores, and vi) a commitment intervention. Patients will subsequently be requested to complete the CollaboRATE survey, JSPPE survey, and questions about their experience in relation to the new format of surveys (only if they were in the intervention group) before receiving a text message reminder around 6-weeks followed by a set of deprioritization questions and the 3-part capability, comfort, and calm survey.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Basic Science
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 89 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All new patients English and Spanish speakers

排除标准

  • Cognitive deficiency precluding PROM completion Language other than English or Spanish

研究组 & 干预措施

Intervention Group

Experimental

Patients randomized to intervention receive both usual Patient reported outcome measure (PROM) and new PROMs strategy (on the technology platform for English speakers and on REDCap/Qualtrix for Spanish Speakers) done after rooming.

干预措施: Usual PROMs and new PROMs strategy (Other)

Control group

No Intervention

Patients go through the registration process which includes PROMs completion using Ipads. Enrolled in the room at the end of the visit.

结局指标

主要结局

Completion of deprioritization options 1 or 2 at 6-week follow-up via text or email

时间窗: through study completion, an average of 6 weeks

"1 = I got what I needed" "2 = I didn't receive anything useful" "3 = I'm still receiving care"

Completion of 3-survey patient-reported outcome measure at 6-week follow-up via Text

时间窗: through study completion, an average of 6 weeks

We will assess the completion of 3-survey patient-reported outcome measure at 6-week follow-up via Text.

Completion of answered text

时间窗: through study completion, an average of 6 weeks

We will assess the completion response rate.

Jefferson Scale of Patient's Perceptions of Physician Empathy

时间窗: through study completion, an average of 6 weeks

The Jefferson Scale of Patient's Perceptions of Physician Empathy includes five 7-point scale questions and higher scores indicated greater perceived clinician empathy.

次要结局

未报告次要终点

研究者

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

David Ring

Professor of Surgery and Perioperative Care Department

University of Texas at Austin

研究点 (2)

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