Actively Recruiting

Phase Not Applicable
Age: 50Years - 75Years
All Genders
Healthy Volunteers
ID05534607

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

Age: 50Years - 75Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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

Follow-up

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

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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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