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Habit Building Software Application to Increase Engagement of Vulnerable Populations in the National Diabetes Prevention Program (NDPP) Lifestyle Change Program (LCP)

T

The Institute for Iterative Thinking

Status

Completed

Conditions

Prediabetes

Treatments

Behavioral: FT LCP

Study type

Interventional

Funder types

Industry
Other U.S. Federal agency

Identifiers

NCT06656273
75D30119C06604 (Other Grant/Funding Number)
1300367-20210112

Details and patient eligibility

About

The goal of this clinical trial is to learn whether a companion software application can improve program engagement in the National Diabetes Prevention Program in adults with prediabetes. The main question[s] it aims to answer [is/are]:

Do participants using the software application (the intervention group) have better engagement with the Diabetes Prevention Program than those who do not use the companion software application (the control group)? Are participants using the software application (the intervention group) more likely to stay in the Diabetes Prevention Program longer than those who do not use the companion software application (the control group)?

Participants are those who have signed up for their local Diabetes Prevention Program and agree to be in the study.

Enrollment

450 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • is eligible for and enrolls in a live or distance LCP at a designated study site during the enrollment period of the study
  • has a smartphone or other device able to engage with the FT LCP app
  • can read basic 5th grade English, as used in the FT LCP app

Exclusion criteria

  • Cohorts and sites enrolled in concurrent, similar health app-based studies

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

450 participants in 2 patient groups

FT LCP
Experimental group
Treatment:
Behavioral: FT LCP
Standard LCP
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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