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MyDiaText Text Messaging Intervention for Diabetes

Children's Hospital of Philadelphia (CHOP) logo

Children's Hospital of Philadelphia (CHOP)

Status

Completed

Conditions

Diabetes Mellitus, Type 1

Treatments

Other: MyDiaText

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT02927639
T32DK063688-13S1 (U.S. NIH Grant/Contract)
16-013222

Details and patient eligibility

About

To test a text messaging intervention using MyDiaText and financial incentives to determine whether such an intervention will improve self-reported self-care behaviors in children 12 to 18 years old. The intervention will consist of daily text messages sent to the subject's personal mobile device. Subjects will be incentivized to respond to text messages via a lottery financial incentive. Previously developed text messages based on the American Diabetes Association (ADA) behavior goals will be used for this intervention.

Enrollment

166 patients

Sex

All

Ages

12 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of type 1 diabetes for more than 1 year
  • HbA1c greater than or equal to 8% but less than 14%.
  • Have been seen in diabetes clinic in the last 6 months
  • Owns a personal mobile device with unlimited text messaging plan

Exclusion criteria

  • Non-English speaking
  • Significant cognitive disability or major organ illness
  • Hemolytic anemia

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

166 participants in 2 patient groups

Intervention
Experimental group
Description:
This group will receive the intervention for 6 months. The intervention will consist of daily text messages sent to the subject's personal mobile device in addition to the usual standard care. Subjects will be incentivized to respond to text messages via a financial reward lottery system. Previously developed text messages based on the ADA behavior goals will be used for this intervention.
Treatment:
Other: MyDiaText
Control
No Intervention group
Description:
This group will receive the usual standard of care for 6 months.

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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