Obesity Clinical Trial
— P@WOfficial title:
5-Year Controlled Intervention Trial: Testing DVD Versus Group Delivery of a Weight-Loss Maintenance Intervention in Native Hawaiian- Serving Worksites
Verified date | July 2012 |
Source | University of Hawaii |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
The PILI @ Work project is a 5 year randomized control trial to adapt a weight loss program
for the employees of Native Hawaiian-serving organizations in Hawai'i. The study has two
specific aims:
Specific Aim 1: To adapt and implement a weight loss and weight loss maintenance program in
Native Hawaiian-serving organizations, working with employee representatives to determine
how the intervention can be best implemented with employees at the worksites. Specific Aim
2: Among employees participating in the program, to test whether weight loss maintenance
program in DVD format is as effective as the weight loss maintenance program in a group face
to face format in maintaining weight loss for employees who complete weight loss program.
The investigators hypothesize that the PILI @ Work interventions can be effectively adapted
and implemented in a worksite settings with active participation by employees and employers.
The investigators also hypothesize that overweight (BMI ≥ 25) and obese (BMI ≥ 30) employees
who complete weight loss portion of the intervention, and are randomized to received the
weight loss maintenance intervention via DVD will have similar success at maintaining weight
loss compared to those randomized to PILI Maintenance in group meetings or settings. The
investigators hypothesize that will will also be true for physical functioning,blood
pressure, daily self-weighing, low to moderate fat and low calorie diets, and daily physical
activity.
Status | Completed |
Enrollment | 200 |
Est. completion date | May 2015 |
Est. primary completion date | April 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - persons of any self-reported ethnicity - age 18 years or older - overweight or obese as defined as (BMI) = 25 for Caucasians, NHs, or PIs and > 23 for those with Asian ancestry - willing and able to follow a healthy eating and physical activity regimen that could include 150 minutes of brisk walking per week (or equivalent) and caloric intake control Exclusion Criteria: - prognosed survival < 6 months - planning to terminate employment during the intervention study period (12 months) - pregnancy - any dietary or exercise restrictions that would prevent an individual from fully participating in the intervention protocol (e.g., end-stage renal disease on a renal diet) - any co-morbid condition (physical and mental disabilities) that would prevent the individual from participating in the intervention protocol (e.g., severe arthritis, hemi-paresis, major psychiatric illness, eating disorder) |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | I Ola Lahui | Honolulu | Hawaii |
United States | Ke Ola Mamo, Native Hawaiian Health Care System | Honolulu | Hawaii |
United States | Keiki o ka Aina | Honolulu | Hawaii |
United States | Queen Liliuokalani Children's Center | Honolulu | Hawaii |
United States | Queen's Medical Center | Honolulu | Hawaii |
United States | University of Hawaii, John A Burns School of Medicine | Honolulu | Hawaii |
United States | Queen Liliuokalani Children's Center | Kailua-Kona | Hawaii |
United States | Molokai Community Health Center | Kaunakakai | Hawaii |
Lead Sponsor | Collaborator |
---|---|
University of Hawaii | I Ola Lahui, Inc., Ke Ola Mamo, Keiki o ka Aina, Molokai Community Health Center, Queen Lili'uokalani Children's Center, Queen's Medical Centre |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in weight from baseline to 3-month and 12-month follow up | Change in weight from baseline to 3-month and 12-month follow up. | baseline, 3-months, 12-months | No |
Primary | Change in physical functioning from baseline to 3-month and 12-month follow up | Change in number of feet walked in 6 minutes from baseline to 3-month and 12-month follow up. | baseline, 3-months, 12-months | No |
Secondary | Blood pressure | Change in blood pressure from baseline to 3-month and 12-month follow up. | baseline, 3-months, 12-months | No |
Secondary | Physical Activity Frequency | Change in physical activity frequency from baseline to 3-month and 12-month follow up as measured by a brief 3-item questionnaire assessing frequency of moderate and vigorous physical activity over the last month. | baseline, 3-months, 12-month | No |
Secondary | Fat in Diet | Change in fat in diet from baseline to 3-month and 12-month follow up as measured by a 36-item questionnaire designed to measure the amount of fat in a participant's diet. | baseline, 3-months, 12-months | No |
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