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临床试验/NCT05080595
NCT05080595已完成不适用

Pilot Randomized Controlled Trial of a Need-Based Transportation Assistance Program in Liver Transplant Candidates

University of Southern California2 个研究点 分布在 1 个国家目标入组 261 人开始时间: 2022年1月24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
261
试验地点
2
主要终点
Time to waitlisting for liver transplant

研究概览

简要总结

We propose a rideshare-supported intervention that leverages a partnership with Lyft Health, a HIPAA-secured logistics solution that enables us to provide reliable and efficient transportation for patients. Lyft rides will be provided to patients for any transplant-related medical visits, including but not limited to clinic visits with transplant providers, laboratory testing, and imaging/procedural testing that need to be performed as part of the routine evaluation process and prior to waitlisting for transplant.

详细描述

Transportation barriers are often cited as barriers to healthcare access, leading to delays in care, non-compliance, and lower health outcomes. We hypothesize that access to transportation is a key modifiable social determinant that, if intervened upon, will lead to improvements in equitable access to the liver transplant waitlist (and transplant) for underserved liver transplant candidates.

We propose a rideshare-supported intervention that leverages a partnership with Lyft Health, a HIPAA-secured logistics solution that enables us to provide reliable and efficient transportation for patients. Lyft rides will be provided to patients for any transplant-related medical visits, including but not limited to clinic visits with transplant providers, laboratory testing, and imaging/procedural testing that need to be performed as part of the routine evaluation process and prior to waitlisting for transplant.

Aim 1 is to ascertain the prevalence of transportation barriers among liver transplant candidates and describe the sociodemographic and clinical characteristics of this population. Aim 2 is to pilot a randomized controlled trial of the needs-based app-supported transportation assistance program (TAP-LT) intervention. We will also assess preliminary efficacy, feasibility, patient acceptability, and cost of the intervention. We will conduct a prospective observational survey study (Aim 1) and pilot randomized controlled trial (Aim 2) at a single liver transplant program (Keck Liver Transplant Program at Keck Medical Center).

For the interventional trial, we will have three arms (Figure 2). Participants who report transportation barriers will be randomized 1:1 to either TAP-LT intervention or usual care (no transportation resources or assistance provided). Additionally, participants who report a reliable source of transportation will be included as a secondary control. In this pilot trial, we will enroll 20 participants in each of the three arms. We anticipate initiation of recruitment within 2 months of study approval, recruitment over approximately 6 months, with 6-12 months of intervention and follow-up with the goal of at least 90 days of follow-up after the end of intervention period for all recruited participants. The target population is adult liver transplant candidates who do not have a reliable source of transportation for their healthcare-related visits and needs. We will include adult patients who are eligible for liver transplantation and attend an initial outpatient evaluation visit.

The primary endpoint is the proportion of liver transplant candidates who report barriers to transportation. We will compare sociodemographic and clinical characteristics stratified by transportation status using Chi-square or t-test/Kruskal-Wallis as appropriate. Predictors of transportation barriers will be assessed with univariate and multivariate logistic regression. The primary outcome (time to listing for transplant waitlisting) will be a time-to-event outcome and we will examine the effect of the TAP-LT intervention with intention-to-treat Fine and Gray competing risk regression based on treatment arm. Secondary outcomes will be compared using Chi-square or t-test/Kruskal-Wallis as appropriate.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Health Services Research
盲法
None

入排标准

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

入选标准

  • Adults (18+)
  • Attended Phase 1 or Phase 1/2 Liver Transplant clinic visit

排除标准

  • Unable to provide informed consent
  • Pregnant women or prisoners
  • Deemed ineligible for liver transplantation during initial evaluation visit
  • Not referred for Phase 2 visit at the time of Phase 1 visit among those with initial Phase 1 visit only
  • Hospitalized at the time of initial Phase 1 or Phase1/2 visit
  • No access to handheld or landline telephone
  • Residence outside of 60 miles from Keck Hospital

研究组 & 干预措施

Transportation assistance, reports unreliable transportation

Experimental

Lyft rides provided to transplant-related appointments

干预措施: Transportation assistance (Lyft rides) (Other)

No transportation assistance, reports unreliable transportation

No Intervention

No intervention, standard-of-care

Transportation assistance, control

No Intervention

No intervention, standard-of-care

结局指标

主要结局

Time to waitlisting for liver transplant

时间窗: through study completion, an average of 1 year

The primary outcome will be time to waitlisting for liver transplant, defined as time (in days) from initial evaluation visit date to date of official listing for liver transplant in the United Network for Organ Sharing database.

次要结局

  • Time to transplant(through study completion, an average of 1 year)
  • Proportion with reported transportation barriers(1 year)
  • Patient survival at 90 days(through study completion, an average of 1 year)
  • Patient satisfaction with care(through study completion, an average of 1 year)
  • Ride-related data among intervention participants(through study completion, an average of 1 year)
  • Proportion waitlisted/transplanted(through study completion, an average of 1 year)
  • Number of no-shows/cancellations(through study completion, an average of 1 year)
  • Number of hospitalizations(through study completion, an average of 1 year)

研究者

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

Kali Zhou

Assistant Professor

University of Southern California

研究点 (2)

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