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The Impact of Continuous Glucose Monitoring Use on Sleep in Parents of Children With Type 1 Diabetes Mellitus

W

Wolfson Medical Center (WMC)

Status

Withdrawn

Conditions

Type 1 Diabetes

Study type

Observational

Funder types

Other

Identifiers

NCT01425255
0077-11-WOMC

Details and patient eligibility

About

The purpose of this prospective exploratory study is to compare sleep quality and sleep-wake patterns in parents of children with type 1 diabetes (T1D) before and several weeks after initiating using real-time continuous glucose monitoring (RT-CGM) of their children.

Full description

Few weeks before scheduled initiation of RT-CGM use of a child with T1D, the 'dominant parent' (the main caregiver during the nighttime in the family) will obtain an informed consent. This will be done during a routine visit in the diabetes clinic. The participants will complete a sleep quality questionnaire (PSQI) and instructions on care of the actigraph and how to keep complete the daily sleep diary will be given. The participants will be instructed to wear the actigraph for 7 consequences nights. Four to eight weeks after initiation of RT-CGM use, the 'dominant parent' will be asked to wear the actigraph for 7 consequences nights and to complete the sleep quality questionnaire and the daily sleep diary.

Sex

All

Ages

20 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Parents of children up to 16 years old with type 1 diabetes

Exclusion criteria

  • Either the child or parent had obstructive sleep apnea, narcolepsy, or restless legs syndrome.

Trial design

0 participants in 1 patient group

Parents of children with Type 1 diabetes
Description:
before and several weeks after initiating using RT-CGM of their children.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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