跳至主要内容
临床试验/NCT05390411
NCT05390411Enrolling By Invitation不适用

Seeking Objectivity in Allocation of Advanced Heart Failure (SOCIAL HF) Therapies Trial

Indiana University1 个研究点 分布在 1 个国家目标入组 1,463 人开始时间: 2023年3月6日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
1,463
试验地点
1
主要终点
Change in SOCIAL HF fidelity from time of training completion (month 2) to time study target has been reached (up to 2 years) and 6 months after reaching study target (up to 2.5 years)

研究概览

简要总结

The primary goal of this study is to assess real-world effectiveness and implementation of an evidence-based multi-component strategy to reduce disparities in the allocation rate of advanced heart failure therapies, heart transplants and ventricular assist devices. This study proposes to implement evidence-based strategies that reduce unequal and unethical decision-making towards patients, replace subjective evaluations with objective criteria, and improve group dynamics in a randomized cluster trial. Our rigorously designed trial will inform national guidelines for advanced heart failure therapy allocation, and data are likely to be generalizable to other organ replacement treatments and advanced chronic disease decision-making processes across populations.

详细描述

Standardized protocols can reduce the impact of unfair and unequal treatment but are underused. Since the Institute of Medicine's report, "Unequal Treatment", multiple studies have confirmed that standardization of decision-making processes reduces unequal treatment, but unequal and unethical perceptions in decision-making in the allocation of advanced therapies has not been addressed. Using an evidence-based framework for behavior change [Capability, Opportunity, and Motivation for Behavior Change/Behavior Change Wheel (COM-B/BCW)], we developed a standardized protocol strategy, Seeking Objectivity in Allocation of Advanced Heart Failure (SOCIAL HF), that addresses the most significant barriers to equality in advanced therapies: 1) unequal and unethical perceptions that influence decision-making, 2) subjectivity in evaluation of social support and adherence, and 3) poor group dynamics. Thus, SOCIAL HF includes: 1) evidence-based training to reduce disparities tailored for HF, 2) restriction to objective evaluations of social support and adherence, and 3) environmental restructuring and modeling of meeting settings to include anonymous electronic voting and more fair-minded seating arrangement. In complex decision-making that includes individuals and groups, our standardized protocol strategy, SOCIAL HF, has the greatest likelihood of reducing health disparities in advanced HF. Our goal is to assess real-world effectiveness (Aim 1) and implementation (Aim 2) of SOCIAL HF for allocation of advanced HF therapies, heart transplant and ventricular assist device implantation. As a type 2 effectiveness-implementation hybrid study, we will use a cluster randomized design to test the effectiveness of SOCIAL HF strategy. We will evaluate implementation of SOCIAL HF across study sites using mixed-methods to learn optimal implementation strategies to reduce disparities in accessing life-saving therapies. We will use normalization process theory to evaluate how SOCIAL HF affects processes and outcomes important to advanced HF centers (e.g. fidelity/variation). We will use RE-AIM framework (reach, effectiveness, adoption, implementation, and maintenance) to evaluate factors that promote reach and adoption and resources needed for implementation. We have the relationships, infrastructure, and expertise to execute this project; our multidisciplinary team includes experts in HF, evidence-based training in reducing unequal and unethical perceptions in decision-making, clinical trials, mixed-methods, and implementation science.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • •Active United Network for Organ Sharing heart transplant and ventricular assist device center
  • •Centers that routinely evaluate at least 50 minoritized racial/ethnic patients and 50 women for advanced heart failure therapies (heart transplant and ventricular assist device) over 2 years
  • •Advanced therapy professionals from participating centers (i.e., coordinators, physicians, pharmacists, nurses, social workers)
  • •Participants for the interview portion will be a subset of otherwise eligible advanced therapy professionals who are included on selection meeting attendance sheets at an included center

排除标准

  • •Centers unable to fully participate in the training and evaluation measures
  • •If the center ceases to be an active heart failure/transplant center

研究组 & 干预措施

Control Sites

No Intervention

No Intervention

Sites Randomized to SOCIAL HF

Experimental

SOCIAL HF is composed of evidence-based disparities reduction training, employment of objective measures of social support, and changes to facilitate group dynamics.

干预措施: SOCIAL HF (Behavioral)

结局指标

主要结局

Change in SOCIAL HF fidelity from time of training completion (month 2) to time study target has been reached (up to 2 years) and 6 months after reaching study target (up to 2.5 years)

时间窗: Month 2, up to 2 years, and up to 2.5 years

Evaluated as barriers, facilitators, and variability in adoption, reach, implementation and maintenance through structured interviews. Study target is defined as time 50 patients of color and 50 women have been evaluated for advanced heart failure therapies per center.

Proportion of evaluated minoritized racial/ethnic patients and women patients receiving advanced therapies.

时间窗: Up to 2 years

Change in SOCIAL HF fidelity from time of training completion (month 2) to time study target has been reached (up to 2 years) and 6 months after reaching study target (up to 2.5 years)

时间窗: Month 2, up to 2 years, and up to 2.5 years

Evaluated as barriers, facilitators, and variability in adoption, reach, implementation and maintenance through structured interviews. Study target is defined as time 50 patients of color and 50 women have been evaluated for advanced heart failure therapies per center.

次要结局

  • Change from baseline sum group function scores at 2 months and time at which study target has been reached (up to 2 years)(Baseline, 2 months, and up to 2 years)
  • Adoption of SOCIAL HF(2 months)
  • Reach of SOCIAL HF(From 2 months up to 2 years)
  • Implementation of SOCIAL HF(From 2 months up to 2 years)
  • Change from baseline knowledge, attitudes, and self-reported behavior change among clinicians at 2 months and time at which study target has been reached (up to 2 years)(Baseline, 2 months, and up to 2 years)
  • Change from baseline knowledge, attitudes, and self-reported behavior change among clinicians at 2 months and time at which study target has been reached (up to 2 years)(Baseline, 2 months, and up to 2 years)
  • Discussion themes during allocation meetings across patient race/ethnicity and sex(Baseline, 2 months, and up to 2 years)
  • Change from baseline sum group function scores at 2 months and time at which study target has been reached (up to 2 years)(Baseline, 2 months, and up to 2 years)
  • Adoption of SOCIAL HF(2 months)
  • Reach of SOCIAL HF(From 2 months up to 2 years)
  • Implementation of SOCIAL HF(From 2 months up to 2 years)

研究者

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

Khadijah Breathett, MD, MS, FACC, FAHA, FHFSA

tenured Associate Professor of Medicine

Indiana University

研究点 (1)

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