Actively Recruiting
Natives Engaged in Alzheimers Research - 'Ike Kupuna (Elder Wisdom) Project
Led by University of Hawaii · Updated on 2024-08-01
192
Participants Needed
3
Research Sites
97 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate the effects of a hula-based program on improving vascular risk factors linked to Alzheimer's disease and related dementias (ADRD), as well as cognitive complaints and function in Native Hawaiian and other Pacific Islander adults aged 50 to 75 years. Participants must have at least one modifiable vascular risk factor such as hypertension, high blood sugar, obesity, or high cholesterol, along with either subjective cognitive impairment (SCI) or mild cognitive impairment (MCI). The study uses a group-randomized design to understand how this cultural physical activity impacts health over 12 months. Participants are divided into two groups: the intervention group receives the Ola Mau i ka Hula program immediately for 12 months, which includes an 8-month active hula lesson phase followed by a 4-month self-monitoring period. The hula program starts with twice-weekly 60-minute classes for 12 weeks, then shifts to monthly 60-minute lessons with weekly 90-minute meetings that combine hula practice and lifestyle education. The control group waits during this time and receives only educational materials and usual medical care, with the option to join the hula program after completing their 12-month assessment. Throughout the study, participants undergo assessments of vascular health markers like blood pressure, cholesterol, blood sugar, and body mass index at 3, 8, and 12 months, alongside cognitive tests and questionnaires to track changes in memory, thinking skills, physical function, and mental health. These measurements help researchers understand the impact of the hula intervention on both physical and cognitive health. The total participation lasts one year, including data collection and follow-up.
CONDITIONS
Brief Title
Natives Engaged in Alzheimers Research - 'Ike Kupuna
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Self-reported Native Hawaiian or other Pacific Islander ancestry
- Age 50 to 75 years
- Has subjective cognitive impairment or mild cognitive impairment
- Diagnosed with hypertension, diabetes, dyslipidemia, or obesity (BMI 2 30 kg/m2)
- Physically able and willing to engage in moderate physical activity like hula
- Has physician approval to participate in moderate physical activity
You will not qualify if you...
- Currently pregnant
- Actively practicing hula at least once per week
- Clinical diagnosis of Alzheimer's disease or related dementias (mild to severe)
- Diagnosed moderate or greater major depressive disorder or moderate or greater depression on the CES-D scale
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 8 months
Participants in the intervention group take part in the Ola Mau i ka Hula program, which includes 12 weeks of twice-weekly 60-minute hula lessons, followed by 5 months of monthly 60-minute hula lessons and weekly 90-minute meetings with a community-peer educator involving hula practice and lifestyle education. Participants in the wait-list control group continue their usual care and receive only the educational component during this time.
Two 60-minute hula classes per week for 12 weeks, then monthly 60-minute hula lessons plus weekly 90-minute meetings for 5 months
Duration - 4 months
Participants continue with a 4-month self-monitoring period after the intervention program ends to observe ongoing effects.
Periodic assessments during self-monitoring period
Trial Site Locations
Total: 3 locations
1
Kula No Na Po'e
Honolulu, Hawaii, United States, 96813
Actively Recruiting
2
Kokua Kalihi Valley
Honolulu, Hawaii, United States, 96819
Actively Recruiting
3
Hui No Ke Ola Pono
Wailuku, Hawaii, United States, 96793
Actively Recruiting
Research Team
J
Janice K Worthington, MPH
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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