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vDPP Facilitated With Community Care Coordination

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Yale University

Status

Completed

Conditions

Diabetes Prevention

Treatments

Behavioral: vDPP

Study type

Interventional

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT04195477
U48DP006380-01-01 (Other Identifier)
U48DP006380-01 (U.S. NIH Grant/Contract)
2000026747

Details and patient eligibility

About

The goal of the proposed Implementation Research project is to assess the feasibility of and pathways for implementation of a virtually-delivered DPP (v-DPP) supported by community-based care coordination facilitated by community health workers (CHWs) and hospital-based community nurses (HCNs). The goal of the intervention is to improve body weight, blood pressure, diet quality, and physical activity levels among low-income individuals at risk for type 2 diabetes.

Full description

Specific aims and hypotheses:

  1. Conduct formative research with community partners (via focus groups and interviews with key stakeholders and a small pilot) to assess community, systemic, technology, and structural level barriers to implementation of a virtually-delivered Diabetes Prevention Program.

    Hypothesis: These efforts will identify individual and community needs, barriers, and resources affecting the feasibility of v-DPP implementation. In addition, strategies for facilitating the delivery of the v-DPP to low-income communities will be developed.

  2. In collaboration with community partners, utilize strategies identified in Aim A1 to maximize impact of the v-DDP in target communities, as evidenced by measures of reach, effectiveness, adoption, implementation, and maintenance (RE-AIM) and assess factors influencing RE-AIM outcomes (e.g. social determinants of health, demographic variables, self-efficacy).

    Hypothesis: The v-DPP facilitated by community-based care coordination will produce favorable RE-AIM outcomes. Factors influencing these outcomes will be explored as well.

  3. Demonstrate improvements in body weight, blood pressure, diet quality, and physical activity in low-income individuals at risk for type 2 diabetes who participate in a v-DPP facilitated by community-based care coordination.

    Hypothesis: The v-DPP, facilitated by community-based care coordination provided by CHWs and HCNs, will improve body weight, blood pressure, diet quality, and physical activity levels in the study communities.

  4. Collaborate with community partners to develop and implement a strategic approach to sustain the v-DPP facilitated by community-based care coordination in the study communities and translate it to other community settings.

Hypothesis: The implementation approach will be packaged, including strategies for implementation in different settings and related costs, providing a process for implementation in other low-income communities in our region and nationally.

Enrollment

96 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • BMI ≥ 25 kg/m2, based on self-reported weight and height;
  • Eligible for Medicaid, as determined by self-reported income, household size, and Connecticut state guidelines for Medicaid eligibility;
  • At risk for prediabetes, as evidenced by a score of 5 points or higher on the CDC prediabetes risk screening test. [https://www.cdc.gov/prediabetes/takethetest/]
  • Participants in New Haven must also be residents of an ECC community (Housing Authority).
  • Participants in Derby and Ansonia must demonstrate proof of residency of either town (i.e., bill or other mail addressed to them).

Exclusion criteria

  • Failure to meet inclusion criteria;
  • Anticipated inability to complete study protocol for any reason;
  • Self-reported current eating disorder;
  • Inability to exercise;
  • Non-English speaking;
  • Pregnant or planned pregnancy in next 12 months;
  • Self-reported diagnosis of type 1 or type 2 diabetes;
  • Failure to pass vDPP provider's required qualification step assessing readiness to change, when available.

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

96 participants in 1 patient group

vDPP Full Study
Experimental group
Description:
Participants will take part in a 52 week study receiving the vDPP intervention.
Treatment:
Behavioral: vDPP

Trial contacts and locations

2

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Central trial contact

Rafael Perez-Escamilla, PhD

Data sourced from clinicaltrials.gov

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