Your session is about to expire
← Back to Search
Allocation Method for Advanced Heart Failure (SOCIAL HF Trial)
N/A
Waitlist Available
Led By Khadijah Breathett, MD, MS
Research Sponsored by Indiana University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up month 2, up to 2 years, and up to 2.5 years
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to test SOCIAL HF, a set of guidelines to ensure fair allocation of advanced heart failure treatments. It targets patients needing heart transplants or special heart pumps. SOCIAL HF works by reducing bias, using objective criteria, and improving decision-making processes.
Who is the study for?
This trial is for heart transplant and ventricular assist device centers that see at least 50 minority patients and 50 women over two years. It includes professionals like coordinators, physicians, pharmacists, nurses, social workers involved in advanced therapy decisions. Centers not fully able to participate or no longer active are excluded.
What is being tested?
The SOCIAL HF trial tests a strategy aimed at equitable allocation of heart failure therapies by reducing bias and using objective criteria over subjective judgment. The study's design may influence national guidelines on how advanced therapies for chronic diseases are allocated.
What are the potential side effects?
Since this trial focuses on decision-making processes rather than direct patient interventions, it does not involve medical side effects. However, the outcomes could affect how treatments like transplants are distributed among patients.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ month 2, up to 2 years, and up to 2.5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~month 2, up to 2 years, and up to 2.5 years
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
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)
Secondary study objectives
Adoption of SOCIAL HF
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)
Change from baseline sum group function scores at 2 months and time at which study target has been reached (up to 2 years)
+3 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Sites Randomized to SOCIAL HFExperimental Treatment1 Intervention
SOCIAL HF is composed of evidence-based bias reduction training, employment of objective measures of social support, and changes to facilitate group dynamics.
Group II: Control SitesActive Control1 Intervention
No Intervention
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for improving decision-making in high-stakes medical scenarios, such as those studied in the Multi-component Strategy trial, focus on reducing bias, employing objective criteria, and enhancing group dynamics. Reducing bias ensures that decisions are based on objective data rather than subjective opinions, which is crucial for fairness.
Using objective criteria standardizes the decision-making process, making it more transparent and reproducible. Improving group dynamics fosters better communication and collaboration among decision-makers, leading to more balanced and well-considered outcomes.
These mechanisms are essential for ensuring equitable and effective allocation of treatments, such as advanced heart failure therapies.
Patient-Centred Care of Older Adults With Cardiovascular Disease and Multiple Chronic Conditions.An updated systematic review of lung chemo-radiotherapy using a new evidence aggregation method.
Patient-Centred Care of Older Adults With Cardiovascular Disease and Multiple Chronic Conditions.An updated systematic review of lung chemo-radiotherapy using a new evidence aggregation method.
Find a Location
Who is running the clinical trial?
Indiana UniversityLead Sponsor
1,035 Previous Clinical Trials
1,217,516 Total Patients Enrolled
National Heart, Lung, and Blood Institute (NHLBI)NIH
3,922 Previous Clinical Trials
47,759,283 Total Patients Enrolled
1 Trials studying Decision Making
7,818 Patients Enrolled for Decision Making
Khadijah Breathett, MD, MSPrincipal InvestigatorIndiana University
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My treatment center is not equipped for the study's required training and evaluations.My center sees many patients from diverse backgrounds and women for advanced heart failure treatments.You are currently on the waiting list for a heart transplant or have a ventricular assist device.People who work at the hospitals involved in the study, such as doctors, nurses, and pharmacists.
Research Study Groups:
This trial has the following groups:- Group 1: Sites Randomized to SOCIAL HF
- Group 2: Control Sites
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Share this study with friends
Copy Link
Messenger