Testing the Effects of a Text Message Caregiver Support Intervention for Latinos (CuidaTEXT R01)

University of Kansas

Status: Enrolling

Conditions: Alzheimer Disease

Treatments: Behavioral: CuidaTEXT

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT06728436

1R01AG082306 (U.S. NIH Grant/Contract)

150585

Details and patient eligibility

About

The goal of this randomized clinical trial it to test the efficacy of CuidaTEXT, the first Alzheimer's disease and Related Dementias (ADRD) caregiver support intervention to capitalize on text messaging, among Latinos.

Researchers will compare those who receive the CuidaTEXT intervention to those who do not receive the intervention to see if CuidaTEXT effects Latino caregiver stressors and their negative consequences .

Participants will receive a variety of text messages, from automatic to keyword-drive, regarding ADRD education, social support, self-care, ADRD care management, and behavioral symptoms. Participants will also complete measures regarding depressive symptoms, coping, behavioral symptoms, and preparedness for caregiving.

Enrollment: 288 estimated patients

Sex: All

Ages: 18 to 100 years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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288 participants in 2 patient groups

CuidaTEXT

Experimental group

Description:

6 months of CuidaTEXT intervention + 1-month post-treatment

Treatment:

Behavioral: CuidaTEXT

7-Month Waitlist Control

No Intervention group

Description:

Participants allocated to this arm will be offered the opportunity to start CuidaTEXT immediately after their 7 Month follow-up assessment