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Expanding the UTHealth Medical Legal Partnership to Improve Mental Health for Low-Income Individuals

Expanding the UTHealth Medical Legal Partnership to Improve Mental Health for Low-Income Individuals

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03805126
Enrollment
160
Registered
2019-01-15
Start date
2019-02-14
Completion date
2020-09-11
Last updated
2020-11-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health-harming Legal Needs

Brief summary

The aim of this study is to test whether participation of low-income patients with health-harming legal needs (HHLNs) in a medical legal partnership (MLP) results in improved mental health, improved quality of life, reduced utilization, and increased resolution of HHLNs.

Interventions

BEHAVIORALMedical Legal Partnership

With the medical legal partnership, lawyers are embedded in clinics, and lawyers consult with patients who are identified as having health-harming legal needs (HHLNs). This arm will also receive usual care, which includes consultation with a social worker and a community health worker.

BEHAVIORALUsual Care

Usual care includes consultation with a social worker and a community health worker.

Sponsors

Texas Medical Center Foundation
CollaboratorUNKNOWN
University of Houston
CollaboratorOTHER
William Marsh Rice University
CollaboratorOTHER
The University of Texas Health Science Center, Houston
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* low-income individuals (Low-income is defined as earning less than 200% of the Federal Poverty Level) * individuals with HHLNs * English or Spanish speaking

Exclusion criteria

* self-identified as being at significant and immediate risk due to HHLNs (e.g., a situation that involves imminent risk to the patient such as domestic violence)

Design outcomes

Primary

MeasureTime frameDescription
Stress as assessed by the Perceived Stress ScalebaselineThe perceived stress scale consists of 10 items, with each item ranging from 0-4, for a total score range of 0-40. A higher score indicates a worse outcome.

Secondary

MeasureTime frameDescription
Depression as assessed by the Center for Epidemiologic Studies Depression ScalebaselineThe Center for Epidemiologic Studies Depression Scale consists of 20 items, with each item ranging from 0-3, for a total score range of 0-60. A higher score indicates a worse outcome.
Quality of life as assessed by the Patient-Reported Outcomes Measurement Information System (PROMIS)baselineThe Patient-Reported Outcomes Measurement Information System (PROMIS) consists of 29 items, with 28 of the items ranging from 1-5 and 1 item ranging from 0-10, for a total score range of 28-150. A higher score indicates a worse outcome.
Number of Urgent Care Visitsbaseline
Anxiety as assessed by the Generalized Anxiety Disorder 7-item scalebaselineThe Generalized Anxiety Disorder scale consists of 7 items, with each item ranging from 0-3, for a total score range of 0-21. A higher score indicates a worse outcome.
Number of Hospital Visitsbaseline
Percentage of baseline health-harming legal needs that were resolvedbaseline
Number of Emergency Department Visitsbaseline

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026