Clinical trial Recruiting at 1 site Interventional Ages 18 to 100

Text message support for Latino caregivers of Alzheimer's patients

Official title: Testing the Effects of a Text Message Caregiver Support Intervention for Latinos

Run by University of Kansas Medical Center · NCT06728436 · Data updated 2026-11-12

This study tests if a text messaging program can help Latino caregivers of Alzheimer's patients feel less stressed and more supported compared to regular care.

More Alzheimer Disease trials

Quick facts

Study typeInterventional
Ages18 Years to 100 Years
SexAll
Enrollment288 (estimated)
SponsorUniversity of Kansas Medical Center
Academic / other
Locations1 site (Fairway, Kansas)
StatusRecruiting
StartedFebruary 17, 2025
Main results expectedMay 2029
Study endsMay 2029
Registry record updatedNovember 9, 2026
Trial IDNCT06728436 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are Latino caregivers over 18 who provide hands-on care for a relative diagnosed with Alzheimer's disease and experience depressive symptoms.

Probably not a fit

Patients who are not caregivers for someone with Alzheimer's disease or who are already participating in another similar intervention may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial aims to evaluate the effectiveness of CuidaTEXT, a text messaging intervention designed to support Latino caregivers of individuals with Alzheimer's disease and related dementias. Participants will be randomly assigned to receive either the CuidaTEXT intervention or standard care, allowing researchers to assess the impact on caregiver stress and related outcomes. The intervention includes a variety of text messages focused on education, social support, self-care, and care management. Participants will also complete assessments regarding their mental health and caregiving preparedness.

Why it matters

Potential benefit: If successful, this intervention could significantly reduce caregiver stress and improve the well-being of Latino caregivers.

How similar studies have gone: Other studies have shown positive outcomes with text message interventions for caregiver support, suggesting potential success for this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Over the age of 18
* Spanish and English-speaking people who identify as Latino
* Reports providing hands-on care for a relative who has been given a clinical or research ADRD diagnosis and has an Eight-item Informant Interview to Differentiate Aging and Dementia (AD-8) screening score ≥2, indicating cognitive impairment
* Has a score of 7 or higher on the 10-item Center for Epidemiologic Studies Depression Scale (CESD-10)
* Self-reports being able to read and write
* Owns a cell phone with a flat fee, and uses it at least weekly for texting.

Exclusion Criteria:

* Participation in another wellbeing-related clinical trial
* Cohabitation with another participant in the CuidaTEXT R01 Study
* Participants who provide care for a person with ADRD already cared for by another participant in the CuidaTEXT R01 study
* Participant plans to move to another country within seven months

Where it's running

  • University of Kansas Medical Center
    Fairway, Kansas, United States
    Recruiting

Study contacts

  • Principal investigator: Jaime Perales Puchalt, PhD, MPH — University of Kansas Medical Center
  • Study coordinator: Rachel Ruiz
  • Email: rruiz3@kumc.edu
  • Phone: 913-945-5052

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.