Family Management of Type 1 Diabetes in Children

Sponsor

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) (NIH)

Overall Status

Completed

CT.gov ID

NCT00273286

Collaborator

(none)

422

Enrollment

Locations

Arm

37.9

Duration (Months)

105.5

Patients Per Site

2.8

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This is a multi-center, randomized controlled trial to test whether a clinic-integrated, low intensity, multi-component behavioral intervention is effective in preventing the deterioration in glycemic control, treatment adherence, and quality of life that commonly occur during late childhood and early adolescence in youth with type 1 diabetes. The study will also examine mechanisms and processes that influence the effectiveness of family management of diabetes during this developmental period.

Condition or Disease	Intervention/Treatment	Phase
Diabetes Mellitus, Type 1	Behavioral: family diabetes management intervention	Phase 2

Detailed Description

The purpose of this study is to test the effectiveness of a practical, low-cost, low-intensity behavioral intervention that can be integrated directly into diabetes clinic routines. The goal of the intervention is to prevent the deterioration in glycemic control, treatment adherence, and quality of life that often occur during the transition to adolescence in families of youth with type 1 diabetes. Four-hundred and eighty families (120 from each of the four sites) will be randomly assigned by the coordinating center to intervention or standard care conditions. Standard care will be the multidisciplinary management of type 1 diabetes as currently practiced at the clinical sites. Randomization will be stratified by main versus recent-onset subgroup, age, and for the main subgroup, baseline glycosylated hemoglobin level. Families will remain in their respective experimental conditions for 24 months. 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 foster improved disease management capabilities and improved parent-youth communication around and sharing of responsibility for diabetes management. Families will be assessed at home three times and in the clinic four times over the course of the study. Measures include parent, child, and family characteristics that may affect intervention effectiveness, targeted mediators, family interaction, management practices, and glycosylated hemoglobin (HbA1c). Primary outcomes are diabetes management adherence and metabolic control; secondary outcomes are quality of life, health status, and psychosocial status.

Study Design

Study Type:

Interventional

Actual Enrollment :

422 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

Single (Outcomes Assessor)

Primary Purpose:

Prevention

Official Title:

Family Management of Childhood Diabetes Study

Study Start Date :

Jan 1, 2006

Actual Primary Completion Date :

Mar 1, 2009

Actual Study Completion Date :

Mar 1, 2009

Arms and Interventions

Arm	Intervention/Treatment
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.	Behavioral: family diabetes management intervention a clinic-integrated, low intensity, multi-component behavioral intervention

Arm

Intervention/Treatment

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.

Behavioral: family diabetes management intervention

a clinic-integrated, low intensity, multi-component behavioral intervention

Outcome Measures

Primary Outcome Measures

glycemic control [1/2006-3/2009]
HbA1c
treatment adherence [1/2006-3/2009]
Diabetes Self Management Profile

Secondary Outcome Measures

quality of life [1/2006-3/2009]
PedsQL Diabetes

Eligibility Criteria

Criteria

Ages Eligible for Study:

108 Months to 174 Months

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

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.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Nemours Children's Clinic	Jacksonville	Florida	United States	32207-8426
2	Children's Memorial Hospital	Chicago	Illinois	United States	60614
3	Joslin Diabetes Center	Boston	Massachusetts	United States	02215
4	Texas Children's Hospital	Houston	Texas	United States	77030