Experimental Trial of an Employment-Based Housing Program for Adults at Risk of Homelessness (Project HIRE)

May 13, 2026 updated by: Vanessa Schick, The University of Texas Health Science Center, Houston
Employment-Based Housing (EBH) is a novel model that helps unstably housed individuals obtain housing and on-site employment where they are housed. The long-term goal of this project is to examine how housing and vocational services can be integrated into hospital emergency departments (EDs) as a multi-sectoral intervention. The investigators central hypothesis is that EBH provides housing, employment, and health insurance which will reduce acute care use and ameliorate non-medical determinants of health more than standard care models. The rationale is that EBH addresses multiple upstream factors that can prevent recurring use of acute care, and the combination of housing with employment services will have positive synergistic effects. This project has three specific aims: 1) Conduct a three-arm randomized clinical trial comparing EBH to passive (resource list) and active control interventions (basic vocational services) on acute care use as the primary outcome and secondary outcomes related to housing, employment, and health-related quality of life; 2) Understand the experiences of subgroups of participants receiving EBH; and 3) Identify barriers and facilitators to adoption of EBH in public healthcare systems in other cities nationally. To achieve these aims, an EBH program will be integrated into the ED of the largest safety net hospital system in Houston, Texas- the 4th largest city in the United States. The project will include a three-arm randomized trial enrolling 750 participants (250 participants per arm). The three-arm trial allows for the investigation of the unique contribution of housing over other non-medical determinants of health (employment and insurance). Participants will be randomized to one of the three arms and followed for 12 months.

Study Overview

Detailed Description

Research Design/Study Arms. Patients discharged from the emergency department of the largest safety net hospitals in Houston, TX (N=750) will be enrolled in a three-arm pragmatic single-blind randomized controlled trial. Clients will be randomly assigned on a 1:1 ratio to one of the three arms: 1) Employment-Based Housing (EBH) facilitated by Entryway Houston; 2) Passive control intervention (PC) which will involve the provision of a list of available community resources; and 3) Active control intervention (AC) which will involve the provision of basic vocational services. The AC intervention will be modeled somewhat after existing community workforce development programs so there is ecological validity and having this additional treatment arm will strengthen the rigor of the trial. Ensuring that both EBH and AC consistently share key characteristics will allow them to directly compare the EBH model to AC.

Study materials will be available in English and Spanish. Individuals will be screened to determine whether they are at risk of homelessness and have an employment need, are 18+ years old, and report a willingness to pass an employer-mandated drug screening and criminal background checks if required by their employer.

Study Type

Interventional

Enrollment (Estimated)

750

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Texas
      • Houston, Texas, United States, 77030
        • UTHealth Houston

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • English and Spanish-speaking individuals
  • Aged 18+
  • Recently discharged from a Harris Health System emergency departments
  • Screen positive for risk of homelessness and employment need per the Centers Accountable Health Communities Health-Related Social Needs Screening Tool.

Exclusion Criteria:

  • Participants with a conservator
  • Unwillingness to participate a background and drug test

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Employment-Based Housing
Experimental intervention
Employment-based housing (EBH) is an innovative program that delivers housing and employment needs simultaneously. EBH will be delivered by an organization called Entryway which will provide training and employment opportunities in the apartment/multifamily housing industry. Since hires are required to live on-site, employees are provided with housing at the properties where they work at no or very low cost. There are a variety of entry-level positions in the industry (e.g., leasing agent, maintenance/apt technician, maintenance/apt supervisor) which pay well above Texas minimum wage and have opportunities for career advancement. Participants will receive job coaching, resume assistance, and extended training. Once trained, they are provided interview assistance (e.g., transportation) and, upon employment, continue to support through ongoing training and mentorship.
Active Comparator: Vocational Services
Active control intervention
Active control intervention (AC) which will involve the provision of basic vocational services. Our in-house vocational specialists will offer basic hands-on vocational assistance and take advantage of various existing job support resources that already exist through the U.S. Department of Labor, the U.S. Department of Veterans Affairs (VA), and other federal and state agencies. This could include job search support, resume review, application support, job prep, and interview training.
Placebo Comparator: Resources
Passive control intervention
Passive control intervention (PC) which will involve the provision of a list of available community resources. Participants randomized to PC will receive a referral to resources via text, and can self-navigate to whichever resource seems best to them.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Emergency Department (ED) Visits
Time Frame: From enrollment to 12 months after enrollment
The number of ED visits during the study period via administrative data and self-report
From enrollment to 12 months after enrollment

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Employment
Time Frame: From enrollment to 12 months after enrollment
The employment status of the participant will be assessed via an assessment of job acquisition during the follow-up period.
From enrollment to 12 months after enrollment
Housing stability
Time Frame: From enrollment to 12 months after enrollment
Housing assessment used in the Collaborative Initiative to End Chronic Homelessness, assessment of housing situation in previous 30 days, and assessment of housing situation the previous night.
From enrollment to 12 months after enrollment
Health-Related Quality of Life
Time Frame: From enrollment to 12 months after enrollment
Short From Health Survey-8 (SF-8) Health survey, a widely used tool which generates mental health and physical component scores with higher scores indicating more positive health.
From enrollment to 12 months after enrollment
Sleep Quality
Time Frame: From enrollment to 12 months after enrollment
Validated with the Mini Sleep Questionnaire, a widely used scale to assess sleep quality and daytime sleepiness with higher scores indicating reduced sleep quality.
From enrollment to 12 months after enrollment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 9, 2026

Primary Completion (Estimated)

June 30, 2030

Study Completion (Estimated)

June 30, 2030

Study Registration Dates

First Submitted

March 3, 2026

First Submitted That Met QC Criteria

March 9, 2026

First Posted (Actual)

March 13, 2026

Study Record Updates

Last Update Posted (Actual)

May 18, 2026

Last Update Submitted That Met QC Criteria

May 13, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

After the end of the performance period, study data will be uploaded to the OpenICPSR data repository. OpenICPSR is a self-publishing repository for social, behavioral, and health sciences research data. De-identified data from our randomized controlled trial will be made available through this repository for others.

IPD Sharing Time Frame

Data will be shared no later than the time of an associated publication or the end of performance period of the extramural award that generated the data, whichever comes first.

IPD Sharing Access Criteria

Scientific data will be made available at the data repository OpenICPSR. Any identifying variables will not be deposited due to privacy and confidential concerns, but access to the deposited data will otherwise not be controlled.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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