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NCT Number: NCT06475534

The Nuestros Días ("Our Days") Study

The goal of this observational study is to understand how contextual, individual-level, and cultural factors influence the daily and long-term well-being of caregivers of relatives with memory problems or dementia. The study focuses on caregivers from the Hispanic and Latino community. The main questions it aims to answer are:

* What daily factors increase (i.e., risk factors) or decrease (i.e., protective factors) the daily odds of depression and anxiety symptoms reported by caregivers? * How do these symptoms vary over time? * Do variations in depression and anxiety symptoms predict distal health outcomes?

Participants will:

* Complete an online baseline survey to understand their caregiving situation. * Fill out daily surveys online for three weeks about their caregiving experiences and well-being. * Complete two follow-up surveys, along with daily surveys, six and twelve months after the baseline survey.

All the study information and surveys can be completed in English or Spanish based on the participant's preference.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Conditions

Caregiver Burden Anxiety Anxiety Disorders Behavior Behavioral Symptoms Depression Mental Disorders Personal Satisfaction Psychological Well-Being Stress, Psychological Well-Being, Psychological

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

The University of Alabama at Birmingham

Birmingham, Alabama, 35233, United States

About this study

Hispanic and Latino/a/x/e (H&L) family caregivers of older relatives living with memory problems or dementia often experience poor mental health due to the increased stress associated with caregiving. The purpose of this study is to examine how contextual, individual-level, and cultural factors influence daily and long-term patterns of depression and anxiety symptoms among H&L caregivers. The investigators will collect data at multiple time points to understand their daily experiences and possible relationships among these factors.

After initial contact, potential participants will complete two eligibility surveys to determine if they are a good fit for the study. If eligible, they will receive a study information sheet outlining all procedures, risks, and benefits.

The study will consist of:

  • Baseline Survey: A 45-minute survey to understand the caregiving situation of each participant.
  • Daily Diaries: After completing the baseline survey, participants will fill out daily surveys for 21 days. These 10-minute surveys will ask about their thoughts, feelings, and experiences of the day and will be emailed at 7 pm each night.
  • Follow-Up Phases: Participants will complete two follow-up phases, one at six months and one at twelve months after the baseline survey. Each phase includes an extended follow-up survey and another series of 21 daily diaries.

The results from this study will inform a dynamic framework of H&L caregiver mental health by identifying modifiable intervention targets associated with resilience over time. This study represents a critical step forward in developing effective, culturally sensitive interventions to support the health and well-being of H&L caregivers, who are often under-supported and face significant challenges in their caregiving role.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years or older
  • Identifies as Hispanic or Latino/a/x/e
  • Provides informal care to a relative living with memory problems or dementia
  • Provides care for 4 hours a day to the person living with memory problems or dementia.

Exclusion criteria

  • admission to a nursing home/institutional care for the person living with memory problems or dementia is planned in the next 6 months
  • the potential participant (caregiver) is terminally ill
  • the participant does not have reliable access to the Internet.

Treatment and study plan

Primary outcomes

  1. Daily Depression Symptom Experience

    Time frame: 63 days

    Patient-Reported Outcomes Measurement Information System (PROMIS) Emotional Distress-Depression Short Form, a 4-item scale measuring common symptoms associated with depression.

    Measures common symptoms associated with depression

    4-item Scale 1-5 Likert Scale with 1 indicating "Never" and 5 indicating "Always" Scores range from 4 to 20

    Higher scores indicate higher levels of depressive symptoms

  2. Daily Anxiety Symptom Experience

    Time frame: 63 days

    Patient-Reported Outcomes Measurement Information System (PROMIS) Emotional Distress-Anxiety Short Form, a 4-item scale measuring common symptoms associated with anxiety.

    Measures common symptoms associated with anxiety

    4-item Scale 1-5 Likert Scale with 1 indicating "Never" and 5 indicating "Always" Scores range from 4 to 20

    Higher scores indicate higher levels of anxiety symptoms

  3. Depression

    Time frame: 12 months

    Patient Health Questionnaire-9 (PHQ-9), a 9-item scale for screening, diagnosing, monitoring and measuring the severity of depression.

    9-item Scale 0-3 Likert Scale with 0 indicating "Not at all" and 3 indicating nearly every day" Scores range from 0 to 27

    Scores 0 - 4 = Minimal Depression 5 - 9 = Mild Depression 10 - 14 = Moderate Depression 15 - 19 = Moderate Severe Depression 20 - 27 = Severe Depression

  4. Anxiety

    Time frame: 12 months

    General Anxiety Disorder-7 (GAD-7), a 7-item scale for screening, diagnosing, monitoring and measuring the severity of anxiety.

    7-item Scale 0-3 Likert Scale with 0 indicating "Not at all" and 3 indicating nearly every day" Scores range from 0 to 21

    Scores 0 - 4 = Minimal Anxiety 5 - 9 = Mild Anxiety 10 - 14 = Moderate Anxiety >15 = Severe Anxiety

  5. Resilience

    Time frame: 12 months

    Resilience Scale for Adults: a 33-item scale measuring personal competence, social competence, personal structure, family coherence, and social support.

    14-item scale with 3 subscales (Perception of self, planned future, structured style) 1-7 Likert Scale with 1 indicating "Not true at all" and 7 indicating "Very true"

    Higher scores indicate higher levels of resilience in the indicated subcategory

  6. Health Related Quality of Life

    Time frame: 12 months

    Patient-Reported Outcomes Measurement Information System (PROMIS) Global Health: 10 item scale measuring global health-related quality of life (HRQOL) across 2 domains: physical and mental health.

    10-item Scale 9 Items use 0 to 4 Likert Scale Item 10: 0 to 10 Likert Scale that is recoded to five categories (0 = 1; 1-3 = 2; 4-6 = 3; 7-9 = 4; 10 = 5) Scores range from 0 to 41

    Higher scores indicate better overall mental and physical health

Sponsors and collaborators

Lead sponsor

University of Alabama at Birmingham

Other

Collaborators

  • National Institute on Aging (NIA)

Registry information

Official study title

The Mental Health Experiences of Hispanic and Latinx Dementia Caregivers

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
Jun 26, 2024
Registry last updated
May 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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