Skip to main content
OpenTrials
Completed

NCT Number: NCT02835495

Healthy Living Partnerships to Prevent Diabetes in Veterans Pilot Study

Diabetes and obesity are both major public health concerns and the prevalence of diabetes is even higher in the patient population of the Veterans Administration. This planning project is designed to adapt a successful weight-loss program for delivery through an existing outpatient clinic to reach local Veterans at risk for developing diabetes. The information gathered as a part of this project will be used to plan a larger trial designed to improve the health of Veterans by offering them a diabetes prevention program through their usual source of healthcare.

Completed

Looking for future studies?

Notify Me

Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

W.G. "Bill" Hefner VA Medical Center, Salisbury, North Carolina, United States

Loading trial locations.

About this study

Type II diabetes and its complications disproportionately affect the patient population served by the Department of Veterans Affairs (VA). Recent lifestyle interventions have demonstrated that weight-loss achieved through reductions in calorie intake and increases in physical activity can prevent or delay the onset of diabetes. The Healthy Living Partnerships to Prevent Diabetes (HELP PD), a community-based adaptation of the lifestyle intervention used in the Diabetes Prevention Program, achieved more than a 7% weight loss at 6 months.

In HELP Vets, researchers will test the feasibility of further translating the HELP PD lifestyle intervention, tailored for use in the Veteran population, in the Kernersville Community-Based Outpatient Clinic operated by the VA. The investigators plan to recruit 50 overweight or obese Veterans at high risk for developing diabetes from the existing patient population to participate in a 6-month weight loss intervention led by community health workers who are also Veterans. As VA outpatient clinics have the requisite infrastructure to identify, screen, and enroll participants and access to Veteran community health workers from within their patient populations, they are ideal potential homes for diabetes prevention programming. Data gathered during this planning grant will be used to develop a large-scale study to test implementing the HELP Vets intervention in a larger segment of the Veteran population.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • BMI 25-40 kg/m2
  • Evidence of Pre-Diabetes: all participants will be required to qualify based on evidence of prediabetes from fasting plasma glucose, oral glucose tolerance test, or hemoglobin A1c (HbA1c) taken in the three months.
  • The appropriate ranges for each test are
  • Hemoglobin A1c (HbAlc): 5.7 to 6.4%
  • Fasting Plasma Glucose: 95-125 mg/dL
  • Oral Glucose Tolerance Test: 140-200 mg/dL.
  • Blood measures will be collected from the medical record
  • Prospective participants must be willing to accept randomization to either the lifestyle intervention or the enhanced usual care condition.

Exclusion criteria

  • Currently involved in a supervised program for weight loss
  • Clinical history of diabetes
  • Clinical history of cardiovascular disease (CVD) occurring within the past 6 months, including myocardial infarction, angina, coronary revascularization, stroke, transient ischemic attack (TIA), carotid revascularization, peripheral arterial disease, and congestive heart failure
  • Uncontrolled high blood pressure (BP > 160/100) Potential participants can be re-screened after controlled
  • Pregnancy, planning pregnancy and breast feeding (self-report) during screening; Other chronic disease likely to limit lifespan to less than 2-3 years, including any cancer requiring treatment in past 5 years except non-melanoma skin cancer
  • Chronic use of medicine known to significantly affect glucose metabolism (e.g., corticosteroids, protease inhibitors)
  • Other conditions/criteria likely to interfere with participation and acceptance of randomized assignment, including the following: inability/unwillingness to give informed consent, another household member already randomized to HELP Vets, major psychiatric or cognitive problems (schizophrenia, dementia, self-reported active illegal substance or alcohol abuse), participation in another research study that would interfere with HELP Vets.

Treatment and study plan

HELP Vets Intervention

Behavioral

This intervention involves a dietary weight loss program and an increase in caloric expenditure through moderate physical activity. The primary treatment objectives for the weight loss component of the intervention will be to decrease caloric intake in a nutritionally sound manner so as to produce a weight loss of approximately 0.3 kg per week for a total weight loss of 5-7%. The primary objective for the physical activity component of the intervention will be to promote an increase in home-based energy expenditure to an eventual goal of 180 min/week.

Individual Education Program

Behavioral

Participants will receive two individual sessions with a nutritionist during the first 3 months. In these sessions, the nutritionist will cover basic aspects of healthy eating and activity to support weight loss, discuss existing community resources and increased physical activity and weight loss. These participants will also receive a monthly newsletter on topics related to healthy lifestyle.

Primary outcomes

  1. Recruitment of Study Participants

    Time frame: 6 months

    To characterize the ability to recruit Veterans to participate in this pilot study, the proportion of Veterans screened who are eligible to participate and the proportion of eligible participants who agree to participate will be calculated. The rate of referrals to the program by providers in the local community-based outpatient clinic will also be monitored.

  2. Retention of Study Participants

    Time frame: 6 months

    To characterize the ability to retain Veterans in this pilot study, the percentage of participants who complete the study (attendance at the 6-month assessment visit) as a measure of overall study retention will be calculated.

  3. Adherence to the Lifestyle Weight Loss Intervention

    Time frame: 6 months

    The proportion of intervention sessions attended will be calculated.

Other outcomes

  1. Weight

    Time frame: 6 months

    The means and standard deviations at 6 months will be calculated.

  2. Systolic Blood Pressure

    Time frame: 6 months

    The means and standard deviations at 6 months will be calculated.

  3. Diastolic Blood Pressure

    Time frame: 6 months

    The means and standard deviations at 6 months will be calculated.

  4. Proportion of Participants for Whom Fasting Glucose is Available at 6-months Post-randomization

    Time frame: 6 months

    In order to assess the feasibility of collecting this data from the medical record, the proportion of participants for whom this data is available at 6-months post-randomization (+/- 90 days) will be reported.

  5. Proportion of Participants for Whom Cholesterol (Lipid Panel) is Available at 6-months Post-randomization

    Time frame: 6 months

    In order to assess the feasibility of collecting this data from the medical record, the proportion of participants for whom this data is available at 6-months post-randomization (+/- 90 days) will be reported.

  6. Fasting Glucose

    Time frame: 6 months

    The means and standard deviations at 6 months will be calculated.

  7. Cholesterol (Lipid Panel)

    Time frame: 6 months

    The means and standard deviations at 6 months will be calculated.

Sponsors and collaborators

Lead sponsor

Wake Forest University Health Sciences

Other

Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
  • US Department of Veterans Affairs

Registry information

Official study title

The Healthy Living Partnerships to Prevent Diabetes in Veterans Pilot Study

Acronym: HELP Vets

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Jul 18, 2016
Registry last updated
Sep 24, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.