Chemical Fingerprints of Skeletal Muscle Health in Children With Type 1 Diabetes
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Type 1 Diabetes
- Sponsor
- Duke University
- Enrollment
- 29
- Locations
- 1
- Primary Endpoint
- Change in muscle mass as measured by D3 creatinine dilution method
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
The purpose of this research study is to find out if Type 1 Diabetes (T1D) affects skeletal muscle health and if we can improve glycemic control by improving skeletal muscle health. Participants in this study will have a blood sample and a urine sample collected after taking a single dose of a nontoxic chemical called D3-creatine. Their body composition will be measured by a scale like device. Parents of participating children will also be asked to complete a food and activity questionnaire.
Participants will be in the study for roughly 12 to 24 months. Enrollment will begin once participant signs the consent form. At the 12 month follow-up visit participants will be asked to wear a Garmin physical activity monitor and use the Garmin Connect mobile app for a period of up to 12 months and take a one time Muscle Strength Measurement test.
The greatest risks of this study include the possibility of loss of confidentiality.
Detailed Description
Physical Activity Monitor: This research will look at the relationship of physical activity on skeletal muscle health, by using a Physical Activity Monitor (Garmin vívofit 3): At the 12 month follow-up visit study participant will be asked to wear a Garmin physical activity monitor and use the Garmin Connect mobile app for a period of up to 12 months. The Garmin Connect app will be downloaded onto the parent or guardian's smartphone or tablet. The study team will create a unique study-specific Duke email (e.g. SMHparticipantXXX@duke.edu) and an assign a unique password for each participant. Passwords will be assigned in accordance with applicable Duke Health password security policy requirements. This email address and password will be used solely for account creation and will not be used for communication. No personal information will be used in the study-specific email or password. Study participants are advised to limit personal identifiers entered into mobile applications/third party software only to those that you wish to voluntarily share with others. Study participant is under no obligation to participate in this phase of the study, as is the case with all research, this sub-study is 100% voluntary. Measurement of Muscle Strength: Upper and lower body strength will be measured using tools that give the researchers a snapshot of the strength in specific muscle groups. Participant will be asked to grip or pinch or push or pull against a device that measures the force they generate when doing these tasks, to measure their strength. In addition to muscle strength testing we will be measuring functional endurance by having participant walk for 6 minutes to see how far they can walk in 6 minutes. These measurements will be taken by a physical therapist in coordination with regularly scheduled appointments.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Type 1 diabetes for at least 3 months (defined by American Diabetes Association criteria, with glutamic acid decarboxylase, islet cell or insulin autoantibodies, and insulin requirement.
- •Age ≥6 to 11 (inclusive) years of age
- •Tanner stage 1 and 2 (pre-pubertal and early pubertal) to minimize pubertal effects
- •Normal weight, overweight and obese children with weight maintenance (no recent significant weight loss or gain). Normal weight will be defined as a BMI between the 5th and 85th percentile; overweight will be defined as a BMI at or above the 85th percentile and below the 95th percentile, obesity will be defined as a BMI at or above the 95th percentile for children of the same age and sex
- •Mobile Phone needed for Activity Monitoring device App
Exclusion Criteria
- •Current or recent (within the past month) use of medications affecting IR (oral or inhaled steroids, metformin, thiazolidinediones, or atypical antipsychotics)
- •Genetic syndrome causing diabetes
- •Untreated hypothyroidism
- •Proteinuria, which could affect the metabolomic profiling.
- •Anemia or hemoglobinopathies that could affect HbA1c levels,
- •Underweight or recent weight loss.
Outcomes
Primary Outcomes
Change in muscle mass as measured by D3 creatinine dilution method
Time Frame: Baseline, 1 year
Secondary Outcomes
- Muscle Strength(Baseline (Sub-study))
- Physical Activity(Up to 1 year)
- Endurance(Baseline (Sub-study))