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NCT03364543 Clinical Trial

The UTHealth Medical-Legal Partnership: Improving Health by Addressing Health-Harming Legal Needs

Social Determinants of Health Clinical Trial

Official title:
The UTHealth Medical-Legal Partnership: Improving Health by Addressing Health-Harming Legal Needs

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03364543
Other study ID # 2017-048
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 16, 2018
Est. completion date February 1, 2019

Study information
Verified date November 2020
Source The University of Texas Health Science Center, Houston
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to assess the acceptability, feasibility, and preliminary effectiveness of the UTHealth medical-legal partnerships (MLP) against usual care.

Recruitment information / eligibility
Status Completed
Enrollment 911
Est. completion date February 1, 2019
Est. primary completion date February 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - English- or Spanish- speaking - screen positive for health-harming legal needs (HHLNs) Exclusion Criteria: - Those unable or unwilling to consent to legal services

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Access to the Medical-Legal Partnership Group
The Medical-Legal Partnership Group are lawyers in clinics who address health-harming legal needs.
• Access to social worker and a community worker
Access to social worker and a community worker, but no systematic process for addressing health-harming legal needs.

Locations
Country Name City State
United States The University of Texas Health Science Center at Houston Houston Texas
United States UTHealth Comprehensive Sickle Cell Center Houston Texas

Sponsors (1)
Lead Sponsor Collaborator
The University of Texas Health Science Center, Houston

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of participants who had an emergency department visit 6 months
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