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临床试验/NCT06296368
NCT06296368
招募中
不适用

DISCOVERY: Evaluating a Decision Support Tool for Adults Seen in Hematology/Oncology Clinics

UNC Lineberger Comprehensive Cancer Center1 个研究点 分布在 1 个国家目标入组 500 人2024年6月21日

概览

阶段
不适用
干预措施
Usual Care
疾病 / 适应症
Hematologic Malignancies
发起方
UNC Lineberger Comprehensive Cancer Center
入组人数
500
试验地点
1
主要终点
Difference in COLLABORATE scores between arms
状态
招募中
最后更新
3个月前

概览

简要总结

The purpose of this study is to evaluate whether a novel decision support tool called PRIME (Preference Reporting to Improve Management and Experience), which combines values-elicitation with tailored feedback to patients and providers, improves patient-reported values-concordance of initial treatment decisions compared to usual care.

详细描述

In the last decade, remarkable advances in drug development have led to the approval of 52 new therapies for patients with hematologic malignancies. These new approvals are increasingly enabling clinicians to personalize chemotherapy decisions to achieve what matters most to patients. Therefore, accurately assessing patient preferences is critical to personalizing treatment decisions, particularly among older adults, who face high treatment-related morbidity and/or shorter anticipated survival. Patient preferences have traditionally been inferred from face-to-face conversations. However, numerous studies, including several systematic reviews, have demonstrated that this process alone is inadequate to reliably capture patient preferences. To support standard shared decision making, multiple stakeholders strongly advocate the development of validated patient-reported measures that accurately capture patients' preferences. In recent guidance about the care of older adults with leukemia, the American Society of Hematology explicitly recommends the development of novel decision support tools to address this growing challenge in patient-centered care. Improved shared decision making has been associated with increased patient-reported quality of care and satisfaction, and a reduction in healthcare utilization. This study will determine the effectiveness of a novel decision support tool called "PRIME" (Preference Reporting to Improve Management and Experience) to improve the values-concordance of initial treatment decisions. Using best-worst scaling, a validated values-elicitation method, PRIME provides a personalized report to providers and patients of their most important treatment priorities. In this pragmatic trial, participants will be randomized to receive decision support with PRIME or usual care prior to their first visit with their oncologist. The primary outcome will be clinically significant improvement in values-concordance of the initial treatment decision (on CollaboRATE, a validated 12-point measure).

注册库
clinicaltrials.gov
开始日期
2024年6月21日
结束日期
2028年9月1日
最后更新
3个月前
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

入排标准

入选标准

  • In order to participate in this study a subject must meet all of the eligibility criteria outlined below.
  • Written or verbal informed consent obtained to participate in the study and HIPAA authorization for the release of personal health information.
  • Subjects are willing and able to comply with study procedures based on the judgment of the investigator.
  • Age ≥ 60 years at the time of consent.
  • New patient to either the hematologic malignancies clinic or the bone marrow transplant/cellular therapy clinic.

排除标准

  • All subjects meeting any of the exclusion criteria listed below at baseline will be excluded from study participation:
  • 1\. Dementia, altered mental status, or psychiatric condition that would prohibit the understanding or rendering of informed consent or participation in the intervention.

研究组 & 干预措施

Usual Care

Receive usual care.

PRIME intervention

Receive the PRIME intervention.

干预措施: Preference Reporting to Improve Management and Experience (PRIME)

结局指标

主要结局

Difference in COLLABORATE scores between arms

时间窗: Up to 24 months

The effectiveness of PRIME to improve the value-concordance of treatment decisions in older subjects presenting to hematologic malignancy clinics will be determined by differences in CollaboRATE scores (Percentage in each arm that report perfect scores 15/15) at the post-treatment decision assessment between control and intervention groups. COLLABORATE scores is a Likert scale questionnaire that includes 3 questions rated from 1 to 5. Higher scores represent better patient engagement.

次要结局

  • Difference in COLLABORATE scores between arms in a subgroup of patients(Up to 24 months)

研究点 (1)

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