Acceptance Based Coping Skills for Hispanic/Latino Military Patients With Type 2 Diabetes
Official title: Supporting Access for Latinx Underserved in Diabetes Management (SALUD-M): An Equity-Driven Study of Acceptance Based Coping Skills for Hispanic/Latinx Military Patients With Type 2 Diabetes Mellitus
Run by Baylor College of Medicine · NCT07674628 · Data updated 2026-11-12
A bilingual health coach will lead a 10-week telehealth program to help Hispanic/Latino military patients with type 2 diabetes manage their condition better.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 70 Years |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | Baylor College of Medicine Academic / other |
| Locations | 1 site (San Antonio, Texas) |
| Status | Recruiting |
| Started | July 16, 2026 |
| Main results expected | March 1, 2027 |
| Study ends | June 30, 2027 |
| Registry record updated | July 28, 2026 |
| Trial ID | NCT07674628 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18-70 with type 2 diabetes and HbA1c ≥7%, who self-identify as Hispanic/Latino/Latinx and prefer English or Spanish, treated at the study site.
✕Probably not a fit
Patients without diabetes-related distress or avoidance coping, or those not engaged with behavioral health components, may see limited benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized trial tests a values-based coping program delivered via telehealth to Hispanic/Latino military patients with type 2 diabetes who have suboptimal glycemic control. The 10-week ABaCo Skills Program includes seven online lessons and is led by a bilingual English-Spanish health coach. The study aims to see if ABaCo improves diabetes care and to understand barriers and facilitators for implementing the program in a military treatment setting. It also assesses feasibility and acceptability for patients and clinics. The lead sponsor is Baylor College of Medicine, with collaborators including the American Diabetes Association and military medical centers, and the study site is Brooke Army Medical Center in San Antonio, TX.
Why it matters
Potential benefit: If successful, participants may see improved diabetes self-management and glycemic control, potentially enhancing quality of life.
How similar studies have gone: Previous work suggests culturally tailored, language-concordant behavioral support can help with diabetes management; this trial tests a structured, tech-delivered program in a military population.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients ages 18-70 * Diagnosis of T2DM * Current HbA1c (drawn within 6 months) of 7% or greater (may be taking oral agents or injectables for diabetes control) * Evidence of avoidance coping (score \<48.4 \[published mean\] on the Acceptance and Action Diabetes Questionnaire) or poor self-management skills (score \< published mean on 2+ subscales of the Summary of Diabetes Self-Care, Activities) * Self-described as Hispanic/Latino/Latina/Latinx * Preferred language of English or Spanish, (g) receiving care at the study site clinic. Exclusion Criteria: * End-stage renal disease (on dialysis) * A medical condition or life circumstance that would contraindicate participation * Proliferative diabetic retinopathy precluding participation * Inability to read/comprehend the informed consent process or study instructions * Pregnant or planning to become pregnant in the next 6 months.
Where it's running
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Brooke Army Medical Center
San Antonio, Texas, United States Recruiting
Study contacts
- Principal investigator: Kathryn E Kanzler, PsyD — Baylor College of Medicine
- Study coordinator: Amanda Leal
- Email: amanda.leal3.ctr@health.mil
- Phone: 240-673-8951
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.