Promoting Physical Activity in Older Hispanic/Latino(a) Adults

Official title

De Pie y a Movernos Study: Promoting Physical Activity in Older Hispanic/Latino(a) Adults

Overview

In this randomized controlled trial, study staff will randomize 130 Hispanic/Latino adults without dementia and over age 55 from Southern California and from Kaiser Permanente Washington (State) to either the culturally adapted De Pie physical activity intervention or an active comparison program focusing on general brain health topics. The purpose of this study is to determine if 12 weeks of the culturally adapted and fully remote De Pie y a Movernos intervention improves self-efficacy, habit strength, social support, and enjoyment for physical activity (PA), thus promoting adherence to moderate-intensity physical activity (MIPA) guidelines (150 minutes/week).

Detailed description

Building on the cultural adaptation of our preliminary R61 De Pie pilot study, study staff will randomize 130 Hispanic/Latino adults without dementia and over age 55 from Southern California and from Kaiser Permanente Washington to either the culturally adapted De Pie physical activity intervention or an active comparison program, Healthy Actions and Lifestyles to Avoid Dementia (HALT-AD), focusing on general brain health topics. The investigators will determine if De Pie improves physical activity (Aim 1) and psychosocial mediators (self-efficacy, habit strength, social support, and enjoyment for physical activity, \[PA\]), thus promoting adherence to moderate-intensity physical activity (MIPA) guidelines (150 minutes/week; Aim 2). The intervention period lasts 12 weeks.

The investigators target middle-aged and older Hispanic/Latino adults that are under-studied and have a higher risk of Alzheimer's disease and related dementias (ADRD), compared to non-Hispanic White older adults. Study staff employ a community engaged and collaborative approach to culturally adaptive the intervention framework and a staircase intervention approach designed to build self-efficacy, PA habit strength, social support, and PA enjoyment. Results will inform culturally adapted, theory-based approaches to prevent ADRD in the Hispanic/Latino community.

Interventions

• Behavioral De Pie Intervention
  Participants are guided by a health coach trained in motivational interviewing through 6 biweekly phone sessions. Each session involves reviewing goals and problem-solving barriers from the prior 2 weeks experience; covering a topic related to Step 1 goals (or Step 2 goals if they pass the safety assessment) such as how to enjoy movement, social support, and using your surroundings; and setting goals and an action plan for the following two weeks.
• Other Active Comparison Group: Healthy Actions And Lifestyles To Avoid Dementia (HALT-AD)
  Those in the active comparison program will receive no additional health coaching sessions. They will work through the HALT-AD content at their own pace, setting goals in the online platform as they go.

Primary outcome measures

• Change in Moderate Intensity Physical Activity (MIPA) minutes/day [Time frame: Baseline to 12 weeks]

Secondary outcome measures (4)

• Meet MIPA guidelines of 150 minutes physical activity per week [Time frame: Baseline to 12 weeks]
• Average daily sedentary time [Time frame: Baseline to 12 weeks]
• Average daily light intensity physical activity (LPA) [Time frame: Baseline to 12 weeks]
• Average steps/day [Time frame: Baseline to 12 weeks]

Eligibility criteria

Inclusion criteria

• be 55-89 and self-identify as Hispanic/Latino(a)
• able to participate for up to 20 weeks in the study
• willing to be randomized to the intervention or active comparison program
• willing to follow study procedures depending on program assignment
• available M-F for study phone calls between 8am-5pm
• able to walk one block unassisted,
• able to speak and can read Spanish or English,
• have a smartphone (85% of the Hispanic/Latino(a) population has a smartphone)
• willing to wear an ActiGraph for up to 2 weeks, twice during the course of the study
• willing to complete study questionnaires via weblink, paper, or phone call
• have an email address and be willing to share it with the team
• have a US mailing address where they receive mail regularly (confirmed in pre-screen)

Exclusion criteria are as follows:

• score less than or equal to 4 on the Six-Item Screener (Callahan et al., 2002)
• unable to hear phone conversation, even with a hearing aid
• planned surgeries or travel that would interfere with participation
• had a fall in the last year that resulted in hospitalization
• had a cancer diagnosis that requires treatment in the past year (other than skin cancer)
• had a diagnosis of heart attack or irregular heart beat (arrythmia) in the past year
• been advised recently by their doctor to avoid physical activity
• does not want to share cognitive health information collected during the study with researchers at UCSD
• unwilling to share their email address
• unwilling to obtain an email address if they do not already have one
• currently participating in another institution's physical activity study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Double blind

Primary purpose

Prevention

Study locations

United States · 2 centers

• University of California San Diego — San Diego
• Kaiser Permanente Washington — Seattle

Identifiers

NCT: NCT06362824 · 2094138

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗