TAP-LT: Transportation Assistance Program for Liver Transplant

Sponsor
University of Southern California (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05080595
Collaborator
(none)
60
1
3
34.2
1.8

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Transportation assistance (Lyft rides)
N/A

Detailed Description

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Pilot Randomized Controlled Trial of a Need-Based Transportation Assistance Program in Liver Transplant Candidates
Actual Study Start Date :
Jan 24, 2022
Anticipated Primary Completion Date :
Nov 30, 2022
Anticipated Study Completion Date :
Nov 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Transportation assistance, reports unreliable transportation

Lyft rides provided to transplant-related appointments

Other: Transportation assistance (Lyft rides)
Lyft rides will be provided to patients for any transplant-related medical visits

No Intervention: No transportation assistance, reports unreliable transportation

No intervention, standard-of-care

No Intervention: Transportation assistance, control

No intervention, standard-of-care

Outcome Measures

Primary Outcome Measures

  1. Time to waitlisting for liver transplant [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.

Secondary Outcome Measures

  1. Proportion with reported transportation barriers [1 year]

    Number of patients who report transportation barriers vs those who don't will be obtained from our transportation barriers survey

  2. Proportion waitlisted/transplanted [through study completion, an average of 1 year]

    Proportion waitlisted/transplanted will be obtained from medical records

  3. Number of no-shows/cancellations [through study completion, an average of 1 year]

    Number of no-shows/cancellations will be obtained from medical records

  4. Number of hospitalizations [through study completion, an average of 1 year]

    Number of hospitalizations will be obtained from medical records

  5. Time to transplant [through study completion, an average of 1 year]

    Time to transplant will be obtained from medical records

  6. Patient survival at 90 days [through study completion, an average of 1 year]

    Vital status will be obtained from medical records

  7. Ride-related data among intervention participants [through study completion, an average of 1 year]

    Number of rides, distance/commute time, cost

  8. Patient satisfaction with care [through study completion, an average of 1 year]

    Measured by patient satisfaction survey

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adults (18+)

  • Attended Phase 1 or Phase 1/2 Liver Transplant clinic visit

Exclusion Criteria:
  • 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Keck Transplant Clinic Los Angeles California United States 90033

Sponsors and Collaborators

  • University of Southern California

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Kali Zhou, Assistant Professor, University of Southern California
ClinicalTrials.gov Identifier:
NCT05080595
Other Study ID Numbers:
  • HS-21-00576
First Posted:
Oct 18, 2021
Last Update Posted:
Jan 28, 2022
Last Verified:
Jan 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Kali Zhou, Assistant Professor, University of Southern California

Study Results

No Results Posted as of Jan 28, 2022