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Enrolling by invitation NCT05390411

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

No phase Interventional Implementation Science Heart Transplant Decision Making

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: SOCIAL HF.
Who it may be relevant to
Registry conditions: Implementation Science, Heart Transplant, Decision Making. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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.

Detailed description

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.

Interventions

  • Behavioral SOCIAL HF
    participate in SOCIAL HF training

Primary outcome measures

  • Proportion of evaluated minoritized racial/ethnic patients and women patients receiving advanced therapies. [Time frame: 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) [Time frame: Month 2, up to 2 years, and up to 2.5 years]
Secondary outcome measures (6)
  • 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) [Time frame: Baseline, 2 months, and up to 2 years]
  • Discussion themes during allocation meetings across patient race/ethnicity and sex [Time frame: 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) [Time frame: Baseline, 2 months, and up to 2 years]
  • Adoption of SOCIAL HF [Time frame: 2 months]
  • Reach of SOCIAL HF [Time frame: From 2 months up to 2 years]
  • Implementation of SOCIAL HF [Time frame: From 2 months up to 2 years]

Eligibility criteria

Inclusion criteria

  • 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

Exclusion criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

United States · 1 center
  • Indiana University — Indianapolis

Identifiers

NCT: NCT05390411 · 13943 · R56HL159216 · R01HL159216

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗