The Impact of Mobile Technology on Clinical Outcomes in Children and Adolescents With Type 1 Diabetes

Withdrawn before enrolling · Not applicable

Conditions studied: Diabetes Mellitus, Type 1

In brief

The purpose of this study is to determine whether a simple text message reminder sent to the parent of an child/adolescent with Type 1 Diabetes(or parent and adolescent) is effective in helping the individual(or parent) become more compliant with self-managing the Type 1 Diabetes (T1D). There will be 5 arms: text message sent to parents of children age 8-12 years old with T1D, text messages sent to parents of adolescents ,age 13-18 years old, with T1D,text messages sent to parents of adolescents with T1D as well as the adolescent with T1D,no text message sent to parents of children age 8-12 years, and no text message sent to adolescents or parents of adolescents age 13-18 years old.

Key facts

Study ID

NCT02619487

Run by

University of Louisville

People needed

0

Starts

2019-03-01

Expected to finish

2019-12-13

Last updated by the study team

2018-12-17

Who can join

Age: 8 and older, up to 18. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Be willing to agree to participate(assent) in the study and have the permission of the parent to do so.
• Have a diagnosis of Type 1 diabetes for ≥ one year.
• Be aged 8 to 18 years old.
• Be on insulin therapy for ≥ one year.
• Have a parent/legal guardian with access to a working cell phone or have a parent/legal guardian with access to a working cell phone and have a working cell phone (if 13 years of age or older).
• Utilize one of the following mobile carriers: T-Mobile, Sprint, Verizon, AT\&T, or Virgin Mobile.
• The parent/legal guardian must express intent to maintain a carrier plan for the duration of the study.
• The parent/legal guardian must be able to read English OR the parent/legal guardian and the adolescent must be able to read English.

You may not qualify if…

• Participants, who in the opinion of the investigator, have any contraindication to tight glycemic control.
• Individuals who are unable to undertake blood glucose testing during the study period
• Individuals who are deemed unable or unlikely to comply with the protocol.

Where it is running

• University of Louisville — Louisville, Kentucky, United States

Full record on ClinicalTrials.gov

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