CClinicalTrials.gg
CompletedNCT03270436Updated Dec 9, 2020Results posted

Diabetes Prevention Program Lifestyle Intervention in the Marshallese Population

An interventional study of Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program and Partnership for Improving Lifestyle Intervention Diabetes Prevention Program in Diabetes Mellitus, Type 2, sponsored by University of Arkansas. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-12-09.

Sponsored by University of Arkansas · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
380
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The investigators will conduct a comparative effectiveness cluster-randomized controlled trial (cRCT) of two Diabetes Prevention Program (DPP) lifestyle interventions: a faith-based intervention (Wholeness, Oneness, Righteousness, Deliverance [WORD] DPP); and a Pacific Islander adapted intervention (Partnership for Improving Lifestyle Interventions [PILI] DPP. Each intervention lasted 24 weeks and focused on the importance of healthy eating, being physically active, and maintaining a healthy weight. Eligible participants included overweight and obese Marshallese adults living in Arkansas and Oklahoma. The unit of randomization is at the church level. The primary outcome measure is body weight loss (from baseline weight). As selected by stakeholders, HbA1c, blood pressure, physical activity, and dietary intake will be evaluated as secondary outcome measures. Data collection will take place at baseline (pre-intervention), immediate post-intervention (6 months post-initiation of the intervention), and 6 months post-intervention (12 months post-initiation of the intervention).

Read the detailed description

Background and Rationale

Disparities in type 2 diabetes, pre-diabetes, and obesity among the Marshallese and Pacific Islanders.

The Marshallese are a Pacific Islander population experiencing significant health disparities, with some of the highest documented rates of type 2 diabetes of any population group in the world. Our review of local, national, and international data sources found estimates of diabetes in the Marshallese population (those living in the US and in the Republic of the Marshall Islands) ranging from 20% to 50%, compared to 8.3% for the US population and 4% worldwide. While national prevalence data are limited, 23.7% of Pacific Islanders surveyed by the Centers for Disease Control and Prevention (CDC) in 2010 reported a diagnosis of type 2 diabetes, more than all other racial/ethnic groups. Our pilot research, which includes health screenings with the Marshallese community in northwest Arkansas (n=398), documented extremely high incidence of diabetes (38.4%) and pre-diabetes (32.6%). Our pilot data also revealed similar disparities in one of the strongest risk factors for diabetes-obesity-with 90% of Marshallese participants classified as overweight or obese. Thirty-two percent of those who had pre-diabetes were also overweight or obese. Further compounding these significant disparities in diabetes prevalence and related risk factors, research indicates that Pacific Islanders living in the US are less likely than other racial/ethnic groups to receive preventative or diagnostic treatment, or diabetes education.

Reducing disparities by reducing weight. Overweight/obesity is considered the strongest modifiable risk factor for type 2 diabetes, and even a modest reduction in weight (5-10%) can be clinically meaningful.

Specific aim. Our aim is to compare the effectiveness of achieving weight loss between two Diabetes Prevention Program (DPP) Lifestyle Interventions - the faith-based Wholeness, Oneness, Righteousness, Deliverance (WORD) DPP, and the Pacific Islander culturally-adapted Partnership for Improving Lifestyle Interventions (PILI) DPP - in the Marshallese population using a cluster randomized controlled trial (cRCT).

Study design. The study design is a comparative effectiveness cRCT conducted in church settings or other community setting convenient to the participant group. Churches were selected as the primary setting based on Marshallese stakeholder input.

Randomized participant assignment. Randomization will occur at the church cluster level, with 1:1 assignment of churches to each arm. Churches and community based participant groups will be blocked (i.e., grouped into similar units) according to geographic region and approximate number of adult church members. Randomization will be conducted by a biostatistician or designated investigator, who will have no interactions with potential participants and has no supervisory role with study staff responsible for recruiting, consent, and intervention process.

Recruitment and Consent

Church-based recruitment is specified by stakeholders as culturally appropriate and the community's preferred recruitment method. During recruitment, Marshallese study staff will give presentations and distribute study information in English and Marshallese. Those who express interest will complete an eligibility screener, to determine eligibility. All study information and consent materials will be provided in English and/or Marshallese based upon the participants' preferences. Eligible participants will be provided a copy of the consent to review, and participants will have the opportunity to ask questions, consent, and enroll in the study. The consent process will include providing information to the potential participants and the opportunity to have bilingual Marshallese staff answer questions regarding study participation. The consent document will be given to the participant, and the informed consent process will be documented in the participant's research record.

02

Conditions studied

  • Diabetes Mellitus, Type 2
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Self reported Marshallese
  • 18 years of age or older
  • BMI greater than or equal to 25

Exclusion criteria

Exclusion Criteria:

  • A clinically significant medical condition likely to impact weight (cancer, HIV/AIDS, etc.)
  • Currently pregnant or breastfeeding an infant who is 6 months old or younger
  • Have any condition that makes it unlikely that the participant will be able to follow the protocol, such as terminal illness, plans to move out of the area within 6 months, an inability to finish the intervention, etc.
04

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
380 participants (actual)

Study arms

  • Experimental
    Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program

    The Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program (WORD DPP) is a faith-based diabetes prevention curriculum that teaches participants to connect faith and health to have a healthy weight, eat healthy, and be physically active. The WORD DPP includes 16 modules that are intended to be delivered over a 24 week period, each module approximately 90 minutes in length. The first 8 modules are intended to be delivered weekly. The last 8 modules are intended to be delivered every other week. Participants in the WORD DPP will be encouraged to maintain a daily weight, nutrition, physical activity and prayer log.

    Behavioral: Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program

  • Experimental
    Partnership for Improving Lifestyle Intervention Diabetes Prevention Program

    The Partnership for Improving Lifestyle Intervention Diabetes Prevention Program (PILI DPP) is a family and community based diabetes prevention curriculum that teaches participants to engage their social support (family and community) to have a healthy weight, eat healthy, and be physically active. The PILI DPP includes 14 modules that are intended to be delivered over a 24 week period and each module approximately 90 minutes in length. The first 4 modules are intended to be delivered weekly. The last 10 modules are intended to be delivered every other week. Participants will be encouraged to track their weight, physical activity, and their nutrition in a log on a daily basis.

    Behavioral: Partnership for Improving Lifestyle Intervention Diabetes Prevention Program

Interventions

  • BehavioralWholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program

    Faith based diabetes curriculum that teaches participants to connect faith and health.

  • BehavioralPartnership for Improving Lifestyle Intervention Diabetes Prevention Program

    Family and community based diabetes prevention curriculum that teaches participants to engage their social support to have a healthy weight.

05

What researchers measure

Primary outcomes

  1. Change in Mean Body Weight (kg)

    Change in mean body weight (kg) from baseline to immediate post intervention and 6 months post-intervention. Participant weight (without shoes) was measured in light clothing using a calibrated digital scale at each time point.

    Time frame: Baseline, immediate post-intervention, 6 months post-intervention

Secondary outcomes

  1. Change in Mean HbA1c (%)

    Change in mean HbA1c (NGSP %) from baseline to immediate post-intervention and 6 months post-intervention. A Siemens analyzer (point of care) was utilized to calculate HbA1c levels for each participant at each time point.

    Time frame: Baseline, immediate post-intervention, 6 months post-intervention

  2. Change in Mean Systolic Blood Pressure (mmHg)

    Change in mean systolic blood pressure (mmHg) from baseline to immediate post-intervention and 6 months post-intervention. Blood pressure was measured at each time point with a sphygmomanometer and stethoscope or digital blood pressure device, with participants seated and arm elevated.

    Time frame: Baseline, immediate post-intervention, 6 months post-intervention

  3. Change in Mean Diastolic Blood Pressure (mmHg)

    Change in mean diastolic blood pressure (mmHg) from baseline to immediate post-intervention and 6 months post-intervention. Blood pressure was measured at each time point with a sphygmomanometer and stethoscope or digital blood pressure device, with participants seated and arm elevated.

    Time frame: Baseline, immediate post-intervention, 6 months post-intervention

  4. Change in Sugar-sweetened Beverage Consumption

    Change in participants' sugar-sweetened beverage (SSB) consumption from baseline to immediate post-intervention and 6 months post-intervention. This self-report measure assessed participants' SSB consumption over the past 30 days using two questions from 'Module 14: Sugar Sweetened Beverages' of the Center for Disease Control and Prevention's Behavioral Risk Factor Surveillance System (BRFSS). Participants could respond in number of times per day, per week, or per month. Responses for each question were converted to number of times per day (i.e., self-reported times per week divided by 7 or self-reported times per month divided by 30), resulting in two measures: number times soda was consumed per day and number of times sugar-sweetened fruit drinks, sweet tea, and sports drinks were consumed per day. Per BRFSS guidelines, these two measures were added together to create a total daily SSB consumption rate.

    Time frame: Baseline, immediate post-intervention, 6 months post-intervention

  5. Change in Fruit and Vegetable Consumption

    Change in participants' fruit and vegetable consumption from baseline to immediate post-intervention and 6 months post-intervention. This self-report measure assessed participants' fruit and vegetable consumption over the past three months using three items adapted from: Shannon J, Kristal AR, Curry SJ, Beresford SA. Application of a behavioral approach to measuring dietary change: the fat- and fiber-related diet behavior questionnaire. Cancer Epidemiol Biomarkers Prev. 1997;6(5):355-361. Each of the three items was scored as Often=2; Sometimes=1; Never=0. Items were summed to create a scale score, giving a possible range of scores of 0-6, with higher scores indicating more frequent consumption of fruits and vegetables.

    Time frame: Baseline, immediate post-intervention, 6 months post-intervention

  6. Change in Proportion of Participants Engaging in Sufficient Levels of Physical Activity

    Change in proportion of participants engaging in sufficient levels of physical activity (PA) from baseline to immediate post-intervention and 6 months post-intervention. This measure assessed participants' frequency of engaging in both moderate and vigorous PA over the past month (\>4 times a week, 2-4 times a week, about once a week, etc.). This measure was adapted to include relevant cultural examples of PA from the Dietary Approaches to Stop Hypertension 2 Brief Physical Activity Questionnaire (https://biolincc.nhlbi.nih.gov/media/studies/dashsodium/Forms_Manual.pdf?link_time=2018-11-13_18:06:05.776099). Both items used a 4-point response scale: 1) Rarely or Never; 2) Once a week; 3) 2-4 times a week; and 4) More than 4 times a week. Each 4-point scale for moderate PA and vigorous PA was weighted: 0=Rarely or Never; 1=Once a week; 2=2-4 times a week; and 4=More than 4 times a week. The weights were then summed and dichotomized as follows: ≥4 = sufficient PA and \<4 = insufficient PA.

    Time frame: Baseline, immediate post-intervention, 6 months post-intervention

Other outcomes

  1. Change in Eating Habits Self-efficacy Score

    Change in eating habits self-efficacy from baseline to immediate post-intervention and 6 months post-intervention (12 months post-initiation of the intervention). This self-report measure assessed participants' self-efficacy related to their ability to make healthy eating decisions in the face of real or perceived barriers (e.g. while at social events, while watching television, etc.). This 7-item measure was adapted from items in the original Weight Efficacy Life-Style (WEL) Questionnaire (Clark MM, Abrams DB, Niaura RS, et al. Self-efficacy in weight management. J Consult Clin Psychol. 1991;59(5):739-744). Each of the 7 items are measured via 3 response options ("Yes/Completely Sure"=2; "Maybe/Not Sure"=1; and "No/Not Sure at All"=0), giving a possible range of scores of 0-14, with higher scores indicating higher self-efficacy for making healthy eating decisions in spite of barriers.

    Time frame: Baseline, Immediate post-intervention, 6 months post-intervention

  2. Change in Physical Activity Self-efficacy

    Change in physical activity self-efficacy from baseline to immediate post-intervention and 6 months post-intervention (12 months post-initiation of the intervention). This self-report measure assessed participants' self-efficacy for exercising in the face of real or perceived barriers (e.g., bad weather, exercising alone, etc.). This 9-item measure was adapted from the Self-Efficacy for Exercise (SEE) Scale (Resnick B, Jenkins LS. Testing the reliability and validity of the Self-Efficacy for Exercise scale. Nurs Res. 2000;49(3):154-159. \& Resnick B, Luisi D, Vogel A, Junaleepa P. Reliability and validity of the Self-Efficacy for Exercise and Outcome Expectations for Exercise Scales with minority older adults. J Nurs Measurement. 2004; 12(3):235-247.) Each of the 9 items are measured via 3 response options ("Yes/Completely Sure"=2; "Maybe/Not Sure"=1; and "No/Not Sure at All"=0), giving a possible range of scores of 0-18, with higher scores indicating higher self-efficacy.

    Time frame: Baseline, Immediate post-intervention, 6 months post-intervention

  3. Change in Perceived Family Support for Exercise and Dietary Habits

    Change in perceived family support for exercise and dietary habits from baseline to immediate post-intervention and 6 months post-intervention. This self-report measure was adapted to examine changes in perceived family support for engaging in healthy exercise and dietary habits. This measure consists of a 6-item scale adapted from: Gruber KJ. Social support for exercise and dietary habits among college students. Adolescence. 2008;43(171):557-575. Each of the 6 items are measured via 3 response options ("Often"=2; "Sometimes"=1; and "Never"=0), giving a possible range of scores of 0-12, with higher scores indicating higher perceived family support for exercising and eating healthier.

    Time frame: Baseline, Immediate post-intervention, 6 months post-intervention

06

Results

Posted Dec 9, 2020

Participant flow

Baseline
Participant flow — Baseline
MilestoneWholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention Program
Started213167
Completed212166
Not completed11
Immediate Post-Intervention
Participant flow — Immediate Post-Intervention
MilestoneWholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention Program
Started213167
Completed172111
Not completed4156
6 Months Post-Intervention
Participant flow — 6 Months Post-Intervention
MilestoneWholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention Program
Started213167
Completed173116
Not completed4051

Outcome measures

PrimaryChange in Mean Body Weight (kg)

Change in mean body weight (kg) from baseline to immediate post intervention and 6 months post-intervention. Participant weight (without shoes) was measured in light clothing using a calibrated digital scale at each time point.

Time frame:
Baseline, immediate post-intervention, 6 months post-intervention
Reported as:
Mean · Kilograms
Change in Mean Body Weight (kg)
KilogramsWholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention Program
Baseline86.44 ± 1.6584.32 ± 1.80
Immediate post-intervention86.47 ± 1.7284.40 ± 1.97
6 months post-intervention86.18 ± 1.8483.80 ± 2.10
Statistical analysis
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.3599 (The p-value above reflects results of between-arms analysis of change in mean weight from baseline to immediate post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.3207 (The p-value above reflects results of between-arms analysis of change in mean weight from baseline to 6 months post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
SecondaryChange in Mean HbA1c (%)

Change in mean HbA1c (NGSP %) from baseline to immediate post-intervention and 6 months post-intervention. A Siemens analyzer (point of care) was utilized to calculate HbA1c levels for each participant at each time point.

Time frame:
Baseline, immediate post-intervention, 6 months post-intervention
Reported as:
Mean · Percent Glycated Hemoglobin
Change in Mean HbA1c (%)
Percent Glycated HemoglobinWholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention Program
Baseline7.27 ± 0.307.66 ± 0.33
Immediate post-intervention7.32 ± 0.317.55 ± 0.36
6 months post-intervention7.25 ± 0.337.61 ± 0.38
Statistical analysis
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.5698 (The p-value above reflects results of between-arms analysis of mean change in HbA1c from baseline to immediate post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.4106 (The p-value above reflects results of between-arms analysis of mean change in HbA1c from baseline to 6 months post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
SecondaryChange in Mean Systolic Blood Pressure (mmHg)

Change in mean systolic blood pressure (mmHg) from baseline to immediate post-intervention and 6 months post-intervention. Blood pressure was measured at each time point with a sphygmomanometer and stethoscope or digital blood pressure device, with participants seated and arm elevated.

Time frame:
Baseline, immediate post-intervention, 6 months post-intervention
Reported as:
Mean · mmHg
Change in Mean Systolic Blood Pressure (mmHg)
mmHgWholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention Program
Baseline129.42 ± 2.39128.20 ± 2.60
Immediate post-intervention126.83 ± 2.47119.65 ± 2.82
6 months post-intervention120.75 ± 2.61118.30 ± 2.96
Statistical analysis
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.0293 (The p-value above reflects results of between-arms analysis of mean change in systolic blood pressure from baseline to immediate post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.4686 (The p-value above reflects results of between-arms analysis of mean change in systolic blood pressure from baseline to 6 months post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
SecondaryChange in Mean Diastolic Blood Pressure (mmHg)

Change in mean diastolic blood pressure (mmHg) from baseline to immediate post-intervention and 6 months post-intervention. Blood pressure was measured at each time point with a sphygmomanometer and stethoscope or digital blood pressure device, with participants seated and arm elevated.

Time frame:
Baseline, immediate post-intervention, 6 months post-intervention
Reported as:
Mean · mmHg
Change in Mean Diastolic Blood Pressure (mmHg)
mmHgWholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention Program
Baseline79.60 ± 1.1278.33 ± 1.22
Immediate post-intervention78.50 ± 1.1974.08 ± 1.38
6 months post-intervention76.41 ± 1.2976.24 ± 1.49
Statistical analysis
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.0068 (The p-value above reflects results of between-arms analysis of mean change in diastolic blood pressure from baseline to immediate post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.9181 (The p-value above reflects results of between-arms analysis of mean change in diastolic blood pressure from baseline to 6 months post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
SecondaryChange in Sugar-sweetened Beverage Consumption

Change in participants' sugar-sweetened beverage (SSB) consumption from baseline to immediate post-intervention and 6 months post-intervention. This self-report measure assessed participants' SSB consumption over the past 30 days using two questions from 'Module 14: Sugar Sweetened Beverages' of the Center for Disease Control and Prevention's Behavioral Risk Factor Surveillance System (BRFSS). Participants could respond in number of times per day, per week, or per month. Responses for each question were converted to number of times per day (i.e., self-reported times per week divided by 7 or self-reported times per month divided by 30), resulting in two measures: number times soda was consumed per day and number of times sugar-sweetened fruit drinks, sweet tea, and sports drinks were consumed per day. Per BRFSS guidelines, these two measures were added together to create a total daily SSB consumption rate.

Time frame:
Baseline, immediate post-intervention, 6 months post-intervention
Reported as:
Mean · SSBs consumed per day
Change in Sugar-sweetened Beverage Consumption
SSBs consumed per dayWholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention Program
Baseline1.65 ± 0.162.16 ± 0.17
Immediate post-intervention1.24 ± 0.171.36 ± 0.20
6 months post-intervention1.18 ± 0.171.40 ± 0.20
Statistical analysis
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.5984 (The p-value above reflects results of between-arms analysis of mean change in sugar-sweetened beverages consumed per day from baseline to immediate post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.3376 (The p-value above reflects results of between-arms analysis of mean change in sugar-sweetened beverages consumed per day from baseline to 6 months post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
SecondaryChange in Fruit and Vegetable Consumption

Change in participants' fruit and vegetable consumption from baseline to immediate post-intervention and 6 months post-intervention. This self-report measure assessed participants' fruit and vegetable consumption over the past three months using three items adapted from: Shannon J, Kristal AR, Curry SJ, Beresford SA. Application of a behavioral approach to measuring dietary change: the fat- and fiber-related diet behavior questionnaire. Cancer Epidemiol Biomarkers Prev. 1997;6(5):355-361. Each of the three items was scored as Often=2; Sometimes=1; Never=0. Items were summed to create a scale score, giving a possible range of scores of 0-6, with higher scores indicating more frequent consumption of fruits and vegetables.

Time frame:
Baseline, immediate post-intervention, 6 months post-intervention
Reported as:
Mean · scale score
Change in Fruit and Vegetable Consumption
scale scoreWholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention Program
Baseline3.59 ± 0.153.70 ± 0.16
Immediate post-intervention3.94 ± 0.163.72 ± 0.18
6 months post-intervention4.10 ± 0.163.80 ± 0.18
Statistical analysis
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.2960 (The p-value above reflects results of between-arms analysis of mean change in fruit \& vegetable consumption scores from baseline to immediate post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.1519 (The p-value above reflects results of between-arms analysis of mean change in fruit \& vegetable consumption scores from baseline to 6 months post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
SecondaryChange in Proportion of Participants Engaging in Sufficient Levels of Physical Activity

Change in proportion of participants engaging in sufficient levels of physical activity (PA) from baseline to immediate post-intervention and 6 months post-intervention. This measure assessed participants' frequency of engaging in both moderate and vigorous PA over the past month (\>4 times a week, 2-4 times a week, about once a week, etc.). This measure was adapted to include relevant cultural examples of PA from the Dietary Approaches to Stop Hypertension 2 Brief Physical Activity Questionnaire (https://biolincc.nhlbi.nih.gov/media/studies/dashsodium/Forms_Manual.pdf?link_time=2018-11-13_18:06:05.776099). Both items used a 4-point response scale: 1) Rarely or Never; 2) Once a week; 3) 2-4 times a week; and 4) More than 4 times a week. Each 4-point scale for moderate PA and vigorous PA was weighted: 0=Rarely or Never; 1=Once a week; 2=2-4 times a week; and 4=More than 4 times a week. The weights were then summed and dichotomized as follows: ≥4 = sufficient PA and \<4 = insufficient PA.

Time frame:
Baseline, immediate post-intervention, 6 months post-intervention
Reported as:
Count of participants · Participants
Change in Proportion of Participants Engaging in Sufficient Levels of Physical Activity
ParticipantsWholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention Program
Baseline11278
Immediate post-intervention10863
6 months post-intervention9965
Statistical analysis
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · Mantel Haenszel · p = 0.2824 (The p-value above reflects results of between-arms analysis of change from baseline to immediate post-intervention. Analyses do not include imputed values.)The model includes only the study arm and time interaction.
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · Mantel Haenszel · p = 0.7547 (The p-value above reflects results of between-arms analysis of change from baseline to 6 months post-intervention. Analyses do not include imputed values.)The model includes only the study arm and time interaction.
Other pre-specifiedChange in Eating Habits Self-efficacy Score

Change in eating habits self-efficacy from baseline to immediate post-intervention and 6 months post-intervention (12 months post-initiation of the intervention). This self-report measure assessed participants' self-efficacy related to their ability to make healthy eating decisions in the face of real or perceived barriers (e.g. while at social events, while watching television, etc.). This 7-item measure was adapted from items in the original Weight Efficacy Life-Style (WEL) Questionnaire (Clark MM, Abrams DB, Niaura RS, et al. Self-efficacy in weight management. J Consult Clin Psychol. 1991;59(5):739-744). Each of the 7 items are measured via 3 response options ("Yes/Completely Sure"=2; "Maybe/Not Sure"=1; and "No/Not Sure at All"=0), giving a possible range of scores of 0-14, with higher scores indicating higher self-efficacy for making healthy eating decisions in spite of barriers.

Time frame:
Baseline, Immediate post-intervention, 6 months post-intervention
Reported as:
Mean · scale score
Change in Eating Habits Self-efficacy Score
scale scoreWholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention Program
Baseline10.97 ± 0.2611.46 ± 0.28
Immediate post-intervention11.77 ± 0.2811.92 ± 0.33
6 months post-intervention11.87 ± 0.2811.62 ± 0.32
Statistical analysis
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.6928 (The p-value above reflects results of between-arms analysis of mean change in eating self-efficacy scores from baseline to immediate post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.4947 (The p-value above reflects results of between-arms analysis of mean change in eating self-efficacy scores from baseline to 6 months post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
Other pre-specifiedChange in Physical Activity Self-efficacy

Change in physical activity self-efficacy from baseline to immediate post-intervention and 6 months post-intervention (12 months post-initiation of the intervention). This self-report measure assessed participants' self-efficacy for exercising in the face of real or perceived barriers (e.g., bad weather, exercising alone, etc.). This 9-item measure was adapted from the Self-Efficacy for Exercise (SEE) Scale (Resnick B, Jenkins LS. Testing the reliability and validity of the Self-Efficacy for Exercise scale. Nurs Res. 2000;49(3):154-159. \& Resnick B, Luisi D, Vogel A, Junaleepa P. Reliability and validity of the Self-Efficacy for Exercise and Outcome Expectations for Exercise Scales with minority older adults. J Nurs Measurement. 2004; 12(3):235-247.) Each of the 9 items are measured via 3 response options ("Yes/Completely Sure"=2; "Maybe/Not Sure"=1; and "No/Not Sure at All"=0), giving a possible range of scores of 0-18, with higher scores indicating higher self-efficacy.

Time frame:
Baseline, Immediate post-intervention, 6 months post-intervention
Reported as:
Mean · scale score
Change in Physical Activity Self-efficacy
scale scoreWholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention Program
Baseline13.64 ± 0.4114.24 ± 0.45
Immediate post-intervention13.87 ± 0.4414.72 ± 0.51
6 months post-intervention14.34 ± 0.4413.57 ± 0.50
Statistical analysis
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.1539 (The p-value above reflects results of between-arms analysis of mean change in physical activity self-efficacy scores from baseline to immediate post-intervention. Analyses do not include imputed values)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.1878 (The p-value above reflects results of between-arms analysis of mean change in physical activity self-efficacy scores from baseline to 6 months post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
Other pre-specifiedChange in Perceived Family Support for Exercise and Dietary Habits

Change in perceived family support for exercise and dietary habits from baseline to immediate post-intervention and 6 months post-intervention. This self-report measure was adapted to examine changes in perceived family support for engaging in healthy exercise and dietary habits. This measure consists of a 6-item scale adapted from: Gruber KJ. Social support for exercise and dietary habits among college students. Adolescence. 2008;43(171):557-575. Each of the 6 items are measured via 3 response options ("Often"=2; "Sometimes"=1; and "Never"=0), giving a possible range of scores of 0-12, with higher scores indicating higher perceived family support for exercising and eating healthier.

Time frame:
Baseline, Immediate post-intervention, 6 months post-intervention
Reported as:
Mean · scale score
Change in Perceived Family Support for Exercise and Dietary Habits
scale scoreWholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention Program
Baseline4.99 ± 0.255.50 ± 0.27
Immediate post-intervention6.66 ± 0.276.38 ± 0.31
6 months post-intervention6.48 ± 0.276.46 ± 0.31
Statistical analysis
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.4322 (The p-value above reflects results of between-arms analysis of mean change in family support scale scores from baseline to immediate post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.
  • Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program vs Partnership for Improving Lifestyle Intervention Diabetes Prevention Program · linear mixed effects regression · p = 0.9529 (The p-value above reflects results of between-arms analysis of mean change in family support scale scores from baseline to 6 months post-intervention. Analyses do not include imputed values.)Model includes group, time, g x t interaction, state, age, gender, marital status, employment, education, and accounts for clustering within churches.

Adverse events

Collected over From enrollment to 1 year post-enrollment. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention Program0/213 (0%)0/213 (0%)0/213 (0%)
Partnership for Improving Lifestyle Intervention Diabetes Prevention Program0/167 (0%)0/167 (0%)0/167 (0%)

Baseline characteristics

The total number of participants providing data at baseline data collection.Two enrolled participants failed to provide data at baseline.

Age, Continuous
Age, Continuous(years)Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention ProgramTotal
Mean42.9 ± 10.641.4 ± 12.842.3 ± 11.6
Sex: Female, Male
Sex: Female, Male(Participants)Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention ProgramTotal
Female11797214
Male9569164
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention ProgramTotal
American Indian or Alaska Native000
Asian000
Native Hawaiian or Other Pacific Islander212166378
Black or African American000
White000
More than one race000
Unknown or Not Reported000
Region of Enrollment
Region of Enrollment(participants)Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention ProgramTotal
United States212166378
Weight (kg)
Weight (kg)(kg)Wholeness, Oneness, Righteousness, Deliverance Diabetes Prevention ProgramPartnership for Improving Lifestyle Intervention Diabetes Prevention ProgramTotal
Mean85.4 ± 15.683.4 ± 14.384.4 ± 15.1
07

Study locations

1 site
  • University of Arkansas for Medical Sciences Northwest
    Fayetteville, Arkansas 72703, United States
08

References and documents

Publications

  • McElfish PA, Long CR, Kaholokula JK, Aitaoto N, Bursac Z, Capelle L, Laelan M, Bing WI, Riklon S, Rowland B, Ayers BL, Wilmoth RO, Langston KN, Schootman M, Selig JP, Yeary KHK. Design of a comparative effectiveness randomized controlled trial testing a faith-based Diabetes Prevention Program (WORD DPP) vs. a Pacific culturally adapted Diabetes Prevention Program (PILI DPP) for Marshallese in the United States. Medicine (Baltimore). 2018 May;97(19):e0677. doi: 10.1097/MD.0000000000010677. PubMed 29742712 ↗

Study documents

  • Protocol and statistical analysis plan · Apr 8, 2020

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

09

Registry details

Key details

Study ID
NCT03270436
Lead sponsor
University of Arkansas
Collaborators
Patient-Centered Outcomes Research Institute
Responsible party
Sponsor
First posted
Sep 1, 2017
Start date
Jan 8, 2018
Primary completion
May 14, 2020
Completion
May 14, 2020
Results posted
Dec 9, 2020
Last update
Dec 9, 2020

Study contacts

Pearl McElfish, PhD
principal investigator · University of Arkansas

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2020. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion