N/A N=78 Randomized Single-blind Prevention

Evaluation of a Lifestyle Intervention for Employees With Prediabetes

Prediabetes · Overweight · Obese

Bottom Line

View on ClinicalTrials.gov: NCT01682954 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Oct 2014

Primary outcome: Primary: Body Weight — -5.12; -0.37 kg — p=<0.0001

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Lifestyle counseling (Behavioral)
Age: Adult, Older Adult · 18+ yrs
Sex: All
Sponsor: Ohio State University
Primary completion: May 2014

Outcome Measures

Outcome	Result	p-value
PRIMARY Body Weight	-4.86; -0.35	<0.0001 sig
PRIMARY Body Weight	-4.86; -0.35	<0.0001 sig

Summary

The purpose of this study is to evaluate the impact of a worksite lifestyle intervention for diabetes prevention among employees with prediabetes.

Eligibility Criteria

Inclusion Criteria

18-65 years old
overweight or obese
prediabetes with elevated glucose value

Exclusion Criteria

recent cardiovascular event
use of corticosteroids
concurrent participation in a structured weight loss program
pregnant or lactating

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01682954). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.