Skeletal Muscle Health in Children With Type 1 Diabetes

Sponsor
Duke University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04288063
Collaborator
(none)
29
1
36.4
0.8

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase

    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.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    29 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Chemical Fingerprints of Skeletal Muscle Health in Children With Type 1 Diabetes
    Actual Study Start Date :
    Sep 18, 2020
    Anticipated Primary Completion Date :
    Oct 1, 2022
    Anticipated Study Completion Date :
    Oct 1, 2023

    Arms and Interventions

    Arm Intervention/Treatment
    Early onset T1D children

    25 young, prepubertal and very early pubertal (Tanner stages 1 and 2) children (13 females and 12 males) with early onset T1D

    Outcome Measures

    Primary Outcome Measures

    1. Change in muscle mass as measured by D3 creatinine dilution method [Baseline, 1 year]

    Secondary Outcome Measures

    1. Physical Activity [Up to 1 year]

      Continuously monitor physical activity of step count using a mobile device (Garmin).

    2. Endurance [Baseline (Sub-study)]

      Measured by a 6 minute walk test of physical activity endurance

    3. Muscle Strength [Baseline (Sub-study)]

      Determined by use of dynamometry measurements

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    6 Years to 11 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Duke University Durham North Carolina United States 27705

    Sponsors and Collaborators

    • Duke University

    Investigators

    • Principal Investigator: Pinar Gumus Balikcioglu, MD, Duke University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Duke University
    ClinicalTrials.gov Identifier:
    NCT04288063
    Other Study ID Numbers:
    • Pro00104288
    First Posted:
    Feb 27, 2020
    Last Update Posted:
    Mar 2, 2022
    Last Verified:
    Feb 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 2, 2022