Text message support for Latino caregivers of Alzheimer's patients
Testing the Effects of a Text Message Caregiver Support Intervention for Latinos
NA · University of Kansas Medical Center · NCT06728436
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.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 288 (estimated) |
| Ages | 18 Years to 100 Years |
| Sex | All |
| Sponsor | University of Kansas Medical Center (other) |
| Locations | 1 site (Fairway, Kansas) |
| Trial ID | NCT06728436 on ClinicalTrials.gov |
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.
Who should consider this trial
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.
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.
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 performed: Other studies have shown positive outcomes with text message interventions for caregiver support, suggesting potential success for this approach.
Eligibility criteria
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 this trial is running
Fairway, Kansas
- 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
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Alzheimer Disease