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Caminemos! Trial to Increase Walking Among Sedentary Older Latinos

Not Applicable
Completed
Conditions
Aging
Sedentary Lifestyle
Interventions
Behavioral: The Lifetime Fitness Program
Behavioral: Exercise class
Registration Number
NCT00183014
Lead Sponsor
National Institute on Aging (NIA)
Brief Summary

The purpose of this study is to examine the efficacy of a multifaceted behavioral intervention aimed at raising walking levels among sedentary older Latinos.

Detailed Description

Regular physical activity contributes to the health and quality of life of older adults, but unfortunately only 20% of men and 25% of women aged 65 years and greater meet the minimal national guidelines for physical activity. Older Latinos have higher rates of diseases that are most likely to benefit from physical activity, but have disproportionately high rates of sedentary lifestyle. To address this major public health problem, this study will implement and evaluate a multifaceted intervention to raise and sustain walking levels among older Latinos.

A total of 600 sedentary older Latinos will be recruited from community-based senior centers in the greater Los Angeles region. The specific aims of the study are to test the effect of the intervention on:

1. the change in steps per week measured by digital pedometer from baseline to 1, 12, and 24-month follow-up;

2. self-reported physical activity level and intervening constructs (including expectations regarding aging and self-efficacy expectations for physical activity);

3. psychosocial health constructs, physical performance measures, and clinical health outcomes.

The core of the intervention consists of a series of 4 weekly 1-hour group discussion sessions that utilize attribution retraining techniques from the field of motivational psychology in combination with behavioral strategies based in social cognitive theory. Discussion sessions will be conducted at senior centers and led by a bilingual health educator; each session will be followed by a 1-hour exercise class aimed at increasing strength, flexibility and endurance. During the discussion sessions, the health educator will administer a structured culturally-tailored curriculum in which participants are taught to raise their expectations for physical activity with aging and not to attribute being sedentary to "old age." The 4 weekly sessions will be followed by monthly sessions for 11 months, and sessions every 2 months for the following 12 months (total intervention duration = 24 months). Participants will be randomized to 1 of 2 arms:

1. intervention arm: receiving the discussion session and the exercise class;

2. control arm: receiving just the exercise class with the same frequency and duration as the intervention group.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
600
Inclusion Criteria
  • Aged 60 years or older
  • Self-identifying as Latino/Hispanic
  • Not currently participating in 20 minutes or more of physical activity 3 times a week
  • Willingness to take brief physical activity screening test and if do not pass, provide the name of a physician who has seen the patient in the recent past
Exclusion Criteria
  • Plans to move from the area in the next 24 months
  • Unable to participate in 1-hour group discussion
  • Unable to walk
  • Physician stating that patient is not medically able to participate
  • Family member already participating
  • Substantial cognitive impairment (determined by a screening test)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
1The Lifetime Fitness Programdiscussion session and exercise class
1Exercise classdiscussion session and exercise class
2Exercise classexercise class only
Primary Outcome Measures
NameTimeMethod
Number of steps per week on digital pedometerbaseline and 1, 12, and 24-months
Secondary Outcome Measures
NameTimeMethod
Self-reported physical activity levelbaseline and 1, 12, and 24-months
beliefs about agingbaseline and 1, 12, and 24-months
self-efficacybaseline and 1, 12, and 24-months
health-related quality of lifebaseline and 1, 12, and 24-months
blood pressurebaseline and 1, 12, and 24-months
body mass index (BMI)baseline and 1, 12, and 24-months
physical performance measuresbaseline and 1, 12, and 24-months
hospital daysbaseline and 1, 12, and 24-months
outpatient visitsbaseline and 1, 12, and 24-months
restricted activity daysbaseline and 1, 12, and 24-months
cognitive functionbaseline and 1, 12, and 24-months

Trial Locations

Locations (1)

UCLA Division of Geriatrics

🇺🇸

Los Angeles, California, United States

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