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PowerUp for Health: A Diabetes Prevention Program for Men

Translating the Diabetes Prevention Program to Engage Men From Disadvantaged Areas

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02555631
Enrollment
29
Registered
2015-09-21
Start date
2015-09-30
Completion date
2016-09-30
Last updated
2018-06-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Men, Type 2 Diabetes

Keywords

type 2 diabetes, prevention, men

Brief summary

The purpose of this two-year proposal is to: 1. develop and 2. complete a pilot test of an adaptation of the evidence-based National Diabetes Prevention Program (NDPP) tailored to engage men with prediabetes in disadvantaged communities in New York City. The sites for this pilot study are New York City Parks and recreation centers. Study's main outcome is weight loss of 5-7% baseline weight.

Detailed description

During year one, the multi-disciplinary research team will work closely with the expert and community Advisory Panel and consultants to adapt the standard NDPP curriculum in order to promote increased engagement of men. Engagement is defined in this proposal to include recruitment, group participation and retention in the 16-week program. This modified NDPP♂ (i.e., for men) renamed by the advisory panel as Power Up for Health, will have only NDPP-trained male coaches and male participants, with adaptations to dietary and physical activity messaging and a new behavioral toolbox approach developed for men. By month 10 of year one, investigators will begin implementation of the 16-week pilot studies of the NDPP♂ at 6 NYC Parks and Recreation Department (REC) sites in disadvantaged communities in three of the NYC boroughs currently offering the standard NDPP programming. Investigators will utilize an iterative and adaptive process during the pilot phase to modify recruitment and retention strategies, as well as the NDPP curriculum and activities. The exploratory aim, as feasible, is to then compare the adapted NDPP♂ pilot data to the standard NDPP mixed-gender groups' available data on recruitment, participation, weight loss, and retention of men from similar NYC neighborhoods. The goal will be pilot study data from 15-20 male participants at each REC pilot site-a recruitment goal of 120 male participants. Working in collaboration with the investigators' consultants and Advisory Panel of community leaders and academic experts in men's health promotion, as well as study partners at the NYC Department of Parks and Recreation, investigators will conduct focused outreach to the target populations. The Specific Aims for the Pilot Study are: Aim 1. to collaborate with the expert and community Advisory Panel to complete the adaptation of the NDPP curriculum and the recruitment and retention activities to better engage men with prediabetes from disadvantaged communities of NYC; Aim 2. to assess preliminary indicators of effectiveness of the NDPP♂ with respect to reductions in body weight; Hypothesis 1: Men engaged in the NDPP♂ will have reductions in body weight at 16 weeks at least equivalent to the NDPP goal of 5-7% of their baseline body weight. Aim 3. to examine and describe from pilot data the extent to which recruitment, intervention and retention strategies, tailored for men with prediabetes are associated with improved engagement of the target population; Exploratory Hypothesis 3.1: Recruitment of men to NDPP♂ will occur more rapidly and with less intensive strategies than recruitment of men to the standard NDPP in comparable communities. Exploratory Hypothesis 3.2: Men enrolled in the NDPP♂ will be more engaged in program activities and self-report greater improvements in healthy eating and physical activity compared with men in the standard NDPP. Exploratory Hypothesis 3.3: Men enrolled in the NDPP♂ will have retention rates that are at least equivalent to men in the standard NDPP. All comparison data analyses are exploratory and as data are available. Aim 4. to examine preliminary data to identify demographic, psychosocial, neighborhood, and REC site characteristics associated with differential recruitment, retention and intervention effects in the NDPP♂.

Interventions

BEHAVIORALlifestyle

In this pilot study, each subject will receive the lifestyle intervention of the diabetes prevention program, a modified program for men from disadvantaged neighborhoods--a 16 weekly sessions of 1 hour each session

Sponsors

The New York Academy of Medicine
CollaboratorOTHER
University of Pittsburgh
CollaboratorOTHER
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
Albert Einstein College of Medicine
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* pre-diabetes by ADA risk test or an A1c in past year in prediabetes range * BMI 24 or above (22 for Asians) * male * lives, works or spend much time in the disadvantaged neighborhood of the park site

Exclusion criteria

* cannot read or write in English or Spanish * has diagnosed diabetes * obvious mental disability so as to preclude health behavior changes

Design outcomes

Primary

MeasureTime frameDescription
Change in Weight in PoundsBaseline, 16 weeksthe goal is to lose 5-7% of baseline body weight for pre-diabetic men

Secondary

MeasureTime frameDescription
Number of Men Enrolled During 8 Weeks of Recruitment8 weeksmeasured by numbers of men and the timeframe in which the recruitment takes place;
Number of Sessions Attended16 weekswith a measured goal of at least attendance observed and recorded at 9/16 sessions on average
Number of Participants That Participated in Each Session16 weeksthis is measured by direct observation at selected sessions; report by the lifestyle coach; and discussion during focus groups at the end of the 16 weeks

Countries

United States

Participant flow

Participants by arm

ArmCount
Lifestyle Intervention
In this pilot study, each subject will receive the lifestyle intervention of the diabetes prevention program, a modified program for men from disadvantaged neighborhoods--a 16 weekly sessions of 1 hour each session lifestyle: In this pilot study, each subject will receive the lifestyle intervention of the diabetes prevention program, a modified program for men from disadvantaged neighborhoods--a 16 weekly sessions of 1 hour each session
29
Total29

Baseline characteristics

CharacteristicLifestyle Intervention
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
2 Participants
Age, Categorical
Between 18 and 65 years
27 Participants
Age, Continuous49.9 years
STANDARD_DEVIATION 11.5
Region of Enrollment
United States
29 Participants
Sex: Female, Male
Female
0 Participants
Sex: Female, Male
Male
29 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
0 / 29
serious
Total, serious adverse events
0 / 29

Outcome results

Primary

Change in Weight in Pounds

the goal is to lose 5-7% of baseline body weight for pre-diabetic men

Time frame: Baseline, 16 weeks

ArmMeasureValue (MEAN)
Lifestyle InterventionChange in Weight in Pounds3.8 percentage of body weight lost
Secondary

Number of Men Enrolled During 8 Weeks of Recruitment

measured by numbers of men and the timeframe in which the recruitment takes place;

Time frame: 8 weeks

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Lifestyle InterventionNumber of Men Enrolled During 8 Weeks of Recruitment29 Participants
Secondary

Number of Participants That Participated in Each Session

this is measured by direct observation at selected sessions; report by the lifestyle coach; and discussion during focus groups at the end of the 16 weeks

Time frame: 16 weeks

ArmMeasureValue (NUMBER)
Lifestyle InterventionNumber of Participants That Participated in Each Session25 Participants
Secondary

Number of Sessions Attended

with a measured goal of at least attendance observed and recorded at 9/16 sessions on average

Time frame: 16 weeks

ArmMeasureValue (MEAN)Dispersion
Lifestyle InterventionNumber of Sessions Attended11.7 Sessions AttendedStandard Deviation 3.9

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026