Study on Influencing Factors of Skin Complications Related to Insulin Injection in Children With Type 1 Diabetes Mellitus

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorThe Children's Hospital of Zhejiang University School of Medicine

About this trial

This study was a cross-sectional, observational design without involving random grouping or intervention. From July 2026 to June 2027, 199 children with type 1 diabetes who had received insulin treatment for at least 6 months and their main family caregivers were recruited by a continuous enrollment method from the endocrinology department of a tertiary children's hospital in Zhejiang Province. Qualified investigators conducted on-site distribution and collection of structured questionnaires, collecting general information of the children, the occurrence of skin complications, and the insulin injection behaviors of the caregivers. At the same time, personnel with ultrasound qualifications used a wireless handheld ultrasound combined with a skin lipid caliper to uniformly measure the subcutaneous fat thickness at 8 sites including the abdomen, buttocks, arms, and thighs.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patient meets the diagnostic criteria for T1DM recommended by WHO and is diagnosed with T1DM.

Patient was diagnosed with T1DM for >= 6 months.

Patient has no cognitive or awareness disorders and has the ability to read.

Patient agrees to participate in this study.

Disqualifiers

Patient has acute or chronic complications of diabetes and is unable to cooperate, requiring urgent treatment.

Patient is in a state of disease stress, such as acute infection, surgery, trauma, etc., and is difficult to cooperate with the research.

Patient's family caregiver has unconsciousness or abnormal mental state.

Patient's family caregiver has hearing or language disorders.

Trial population

Children diagnosed with type 1 diabetes and receiving insulin treatment, along with their primary family caregivers

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Prevalence of insulin injection-related lipohypertrophy

The proportion of children with type 1 diabetes who are identified as having insulin injection-related lipohypertrophy. Lipohypertrophy will be determined as present if it is detected by physical examination and/or ultrasound assessment; results from these assessments will be combined into a single yes/no determination for each participant and reported as a proportion.

Time frame
2026.07-2027.06

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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