Family Management of Type 1 Diabetes in Children
Diabetes Mellitus, Type 1
About this trial
This is an interventional prevention trial for Diabetes Mellitus, Type 1 focused on measuring Diabetes Mellitus, Insulin-Dependent, Diabetes Mellitus, Juvenile-Onset, IDDM, Type 1 Diabetes Mellitus
Eligibility Criteria
Child Inclusion Criteria: Age 9.0 to <14.5. Type 1 diabetes diagnosis (diagnosed by ADA criteria) for a minimum of 1 year for the main subgroup or 3 months for the recent onset subgroup. Insulin dose greater than or equal to 0.5 u/kg/day for the main subgroup or 0.2 u/kg/day for the recent onset subgroup; with 2 or more daily injections or use of insulin pump. Most recent A1c is >6.0% and <13.0%; <12.0% for those diagnosed for less than 1 year. Willing to provide informed assent. Parent/Family Environment Inclusion Criteria Child lives in geographically stable home, no multiple foster homes, boarding school, or institutions expected in next 2 years. The same 1 or 2 adult caregivers have accompanied the child to every diabetes clinic visit in the past year, and at least 1 caregiver agrees to participate in all aspects of the protocol (single-parent families, blended families, and separated parents will be eligible). Home has telephone access. Child had at least 2 clinic visits within last 12 months. Parent and child willing to come to clinic every 3 months for duration (2 years) of study. If a family has more than one eligible child, all qualifying children who provide consent/assent will participate in assessment and intervention or control activities; however, only the oldest qualifying child will be included in statistical analyses. Child Exclusion Criteria: Presence of a major chronic diseases (except well-controlled thyroid, asthma, celiac). Presence of a major visual/auditory impairments. Child is in a self-contained special education class throughout the school day. Record of inpatient hospitalization for mental disorder in past six months including substance abuse rehabilitation, eating disorder units or day treatment programs. Current diagnosis of eating disorder. History of anti-psychotic medications for the past 6 months. Diagnosis of mental retardation. Unable to read and write English at 2nd grade level. Children who are currently enrolled in any intervention study are not eligible for enrollment. Those who have been in an intervention arm of a trial of a behavioral, psychological or psychoeducational intervention and concluded their study follow-up within the past 12 months are also ineligible to participate. However, children who were in a standard care control group in an intervention study are eligible once they have completed all scheduled study follow-ups. Children cannot enroll in another intervention study during the course of this study. Enrollment of children who are currently participating in another observational study will be at the discretion of the site principal investigator. Parent/Family Environment Exclusion Criteria Family has plans to re-locate out of area within the next 2 years of the study. Participating caretaker is currently undergoing treatment for substance abuse. Participating caretaker has been hospitalized in past 6 months for mental disorder. Participating caretaker has history of psychosis. Families who are currently enrolled in any intervention study are not eligible for enrollment. Those who have been in an intervention arm of a trial of a behavioral, psychological or psychoeducational intervention and concluded their study follow-up within the past 12 months are also ineligible to participate. However, families who were in a standard care control group in an intervention study are eligible once they have completed all scheduled study follow-ups. Families cannot enroll in another intervention study during the course of this study. Enrollment of families who are currently participating in another observational study will be at the discretion of the site principal investigator. The family must reside within 90 miles (one-way) of the clinic (main or satellite), or agree to meet at a mutually agreed upon closer location for conduct of the home assessment.
Sites / Locations
- Nemours Children's Clinic
- Children's Memorial Hospital
- Joslin Diabetes Center
- Texas Children's Hospital
Arms of the Study
Arm 1
Experimental
family diabetes management intervention
A trained health advisor will be responsible for interactions with parents and patients prior to each diabetes clinic visit (Preparation Phase), at the time of the diabetes clinic visit (Consolidation Phase) and by phone, e-mail, etc. after the clinic visit (Follow-up Phase). Using educational modules developed for the study, families will be engaged in problem identification and solving activities to improve shared parent-youth responsibility for diabetes management and foster increased adolescent's independent management capabilities.