Skip to content

Sí Texas Hope Family Health Center

Sí Texas HOPE: Enhanced Integrated Behavioral Health Model for Uninsured Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03916016
Enrollment
585
Registered
2019-04-16
Start date
2015-12-09
Completion date
2018-03-29
Last updated
2019-04-22

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

Conditions

Chronic Disease, Depression, Diabetes, Hypercholesterolemia, Hypertension, Obesity

Keywords

Integrated Behavioral Health, Integrated Care, Volunteer Clinic

Brief summary

This study evaluated whether uninsured patients living at or below 200% of the federal poverty level who received enhanced, culturally-relevant, integrated behavioral health services were more likely to improve health outcomes after 12 months compared to similar patients receiving usual care from Hope Family Health Center (HFHC), a charitable community clinic. The study employed a randomized control trial (RCT) design where intervention participants receiving integrated care at HFHC were compared to control participants receiving usual care at HFHC. Patients were placed in each group using simple random assignment. Demographic and health outcome data were collected from intervention and control participants at baseline. Health outcome data were subsequently collected at 6-month and 12-month follow-up points.

Detailed description

This study evaluated whether uninsured patients living at or below 200% of the federal poverty level who received enhanced, culturally-relevant, integrated behavioral health services were more likely to improve health outcomes after 12 months compared to similar patients receiving usual care from Hope Family Health Center (HFHC), a charitable community clinic. The study employed a randomized control trial (RCT) design where intervention participants receiving integrated care at HFHC were compared to control participants receiving usual care at HFHC. Patients were placed in each group using simple random assignment. Demographic and health outcome data were collected from intervention and control participants at baseline. Health outcome data were subsequently collected at 6-month and 12-month follow-up points. The primary outcomes of interest were systolic and diastolic blood pressure and depressive symptoms. Additional secondary outcomes of interest were HbA1c and BMI. These outcomes were analyzed as continuous variables using linear regression with backward model selection. Longitudinal analyses were also conducted using a likelihood-based approach to general linear mixed models. The participants (1) resided in Cameron, Hidalgo, Willacy, or Starr County, (2) were eligible to receive behavioral health services from HFHC (e.g., uninsured, living at or below 200% of the federal poverty level, residence in HFHC's service area), and (3) had a diagnosis of hypertension (blood pressure of 140/90 mm Hg or higher) and/or obesity (body mass index of 30.0 or higher) and/or poorly controlled diabetes (HbA1c over 6.8) and/or moderate depression (score of 10 or above on PHQ-9).

Interventions

BEHAVIORALEnhanced Integrated Behavioral Health Care

The intervention involved moving from HFHC's previous collaborative model, where medical and behavioral providers worked with each other episodically, to a more fully integrated collaborative care model with care coordination, shared treatment plans, shared service provision, and shared record keeping. To achieve this enhanced level of integration, HFHC changed its current primary care workflow to include a behavioral health specialist who conducted assessments, provided initial counseling (individual or group), and coordinated referrals to care management and/or community-based health services.

BEHAVIORALUsual Care

A collaborative model where medical and behavioral providers worked with each other episodically

Sponsors

Methodist Healthcare Ministries of South Texas, Inc.
CollaboratorUNKNOWN
Social Innovation Fund
CollaboratorUNKNOWN
Health Resources in Action, Inc.
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Treatment group participants were randomized to receive enhanced integrated behavioral health care. Control group participants received care as usual.

Eligibility

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

Inclusion criteria

* Reside in Cameron, Hidalgo, Starr, or Willacy County * Were eligible to receive behavioral health services from HFHC (e.g., uninsured, living at or below 200% of the federal poverty level, residence in HFHC's service area) * Have a diagnosis of one or more chronic conditions: * Hypertension (blood pressure of 140/90 mmHg or higher) * Obesity (body mass index of 30.0 or higher) * Poorly controlled diabetes (HbA1c over 6.8%) * Moderate depression (score of 10 or above on PHQ-9)

Exclusion criteria

* Not actively suicidal at time of enrollment

Design outcomes

Primary

MeasureTime frameDescription
Blood PressureOne yearBlood pressure was measured as a continuous variable (systolic and diastolic) in millimeters of mercury (mmHg).

Secondary

MeasureTime frameDescription
Body mass indexOne yearHeight and weight were measured at baseline, and body mass index was calculated.
Depressive SymptomsOne yearScore calculated based on responses to the Patient Health Questionnaire-9. The PHQ-9 has a total possible score of 27. Each of the nine questions is assigned a value of 0, 1, 2, or 3. The total score is the sum of individual questions' scores. The PHQ-9 scoring criteria is categorized as minimal (0-4), mild (5-9), moderate (10-14), moderately severe (15-19) and severe (20-27) depression.
Blood glucose concentrationOne yearBlood glucose concentration was measured via blood test for HbA1c as a continuous variable

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026