Blood Glucose Testing and You

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

297 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-10-31

Study Completion Date

2011-11-30

Brief Summary

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The purpose of this study is to determine the difference between self-reported, estimated blood glucose level versus blood glucose levels measured with a Blood Glucose Meter.

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Detailed Description

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Conditions

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Diabetes

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Blinding Strategy

NONE

Study Groups

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People with type 2 diabetes

People with type 2 diabetes who were in attendance at a diabetes conference were asked for their perceived Blood Glucose (BG) value. Then, after staff measured BG on a Blood Glucose meter, subjects were informed of their BG value.

Group Type OTHER

Blood Glucose meter

Intervention Type OTHER

Staff tested subject Blood Glucose using a Blood Glucose meter.

Interventions

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Blood Glucose meter

Staff tested subject Blood Glucose using a Blood Glucose meter.

Intervention Type OTHER

Other Intervention Names

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Contour® Blood Glucose Meter

Eligibility Criteria

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Inclusion Criteria

1. Males and females, 18 years of age and above
2. Type 2 diabetes
3. Able to speak, read, and understand English
4. Willing to complete all study procedures

Exclusion Criteria

1. Type 1 diabetes
2. Currently a user of continuous glucose monitoring system
3. Currently pregnant
4. Hemophilia or any other bleeding disorder
5. Employee of competitive medical device company
6. Cognitive disorder or other condition which, in the opinion of the investigator (or designee), would put the person at risk or seriously compromise the integrity of the study

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No