N/A
Completed N=94
CloudConnect: Predictive And Retrospective Clinical Decision Support For Chronic Disease Management
Source: ClinicalTrials.gov NCT03676465 ↗Enrolled (actual)
94
Serious AEs
2.3%
Results posted
Dec 2023
Primary outcomePrimary: Family Communication Inventory Questionnaire — 12.3; 11.5 Score on a scale — p=>0.05
Summary
This study is to assess an approach of self-management called CloudConnect, evaluating the impact of CloudConnect Reports on patient engagement, adolescent/parent discussion, and clinical outcomes in adolescent Type 1 Diabetes (T1D).
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Family Communication Inventory Questionnaire |
12.3; 11.5 | >0.05 |
| SECONDARY Glucose Time in Range 70-180 mg/dL, Overall |
47.6; 40.4 | >0.05 |
| SECONDARY HbA1c, Final |
7.58; 7.71 | >0.05 |
| SECONDARY Mean Glucose by CGM |
198.2; 201.0 | >0.05 |
| SECONDARY Percent Time <70 mg/dL |
1.1; 1.2 | >0.05 |
| SECONDARY Percent Time >180 mg/dL |
53.6; 54.0 | >0.05 |
| SECONDARY Low Blood Glucose Episodes Per Week |
2.75; 3.3 | >0.05 |
| SECONDARY Family Conflict Scale |
25.4; 24.4 | >0.05 |
| SECONDARY Division of Diabetes Responsibilities Score |
21.3; 23.1 | >0.05 |
| SECONDARY Child Self Management Score |
4; 4 | >0.05 |
| SECONDARY My-Q |
93.5; 95.8 | >0.05 |
| SECONDARY Weekly Diabetes Communication |
88; 89 | >0.05 |
| SECONDARY Tone of Response |
3.58; 3.84 | >0.05 |
| SECONDARY Change of Insulin Parameters |
0.36; 0.12 | <0.001 sig |
Eligibility Criteria
Inclusion Criteria
- Willingness to provide informed consent
- Adolescents ages ≥12 and ≤ 17 years old with a parent/guardian (18+ yo) who is willing to participate with the child
- HbA1c ≥7 and ≤ 11 % (point-of-care machine or local laboratory [i.e. LabCorp]) (*This criteria only applies to the Main Study, it does not apply to the Pilot Study*)
- Willingness and ability to comply with scheduled visits and study procedures
- Willingness to comply with all the study devices during the entire trial (i.e. commercially-available CGM, Fitbit, Companion Medical inPen)
- One month stability on insulin parameters prior to enrollment
- MDI users should use Humalog® and Novolog® insulin to use in study insulin pen
- Type 1 diabetes mellitus diagnosed at least one year prior to enrollment in the study as noted by the following:
Criteria for documented hyperglycemia (at least 1 criterion must be met):
- Fasting glucose ≥ 126mg/dL-confirmed
- Two-hour Oral Glucose Tolerance Test (OGTT) ≥200mg/dL-confirmed hemoglobin A1c (HbA1c) ≥6.5% and documented by history - confirmed Random glucose ≥200 mg/dL with symptoms
- No data at diagnosis is available but the participant has a convincing history of hyperglycemia consistent with diabetes
Criteria for requiring insulin at diagnosis (at least 1 criterion must be met):
- Participant required insulin at diagnosis and continually thereafter
- Participant did not start insulin at diagnosis but upon investigator review likely needed insulin (significant hyperglycemia that did not respond to oral agents) and did require insulin eventually and used continually)
- The diagnosis of type 1 diabetes mellitus does not require documentation of C-peptide level or islet cell antibody positivity.
- Commitment to maintaining uninterrupted availability via cell phone at all times
- No diabetes complications
- Participants must demonstrate English proficiency and proper mental status and cognition for completion of the study.
- Not currently known to be pregnant, breast feeding, or intending to become pregnant (females). A negative urine pregnancy test will be required for adolescent girls who are able to become pregnant. Participants who become pregnant will be discontinued from the study.
- Ability to access the Internet to provide data to the clinical team or to travel to the research center so that the study equipment can be downloaded.
- Medication stability in the preceding two months if taking antihypertensive, thyroid, anti-depressant or lipid lowering medication.
Exclusion Criteria
- Children outside the ages of 12-17 y.o. or those who do not have a parent/guardian willing to participate
- Diabetic ketoacidosis in the past 6 months
- Pregnancy, breast-feeding, or intention of becoming pregnant
- Current or recent alcohol or drug abuse by patient history
- Mental incapacity, unwillingness or language barriers precluding adequate understanding, cooperation, or ability to fill out questionnaires.
- Any skin condition that prevents sensor placement (e.g., bad sunburn, pre-existing dermatitis, intertrigo, psoriasis, extensive scarring, cellulitis)
- Psychiatric disorders that would interfere with study tasks (e.g. cognitive disability, psychiatric hospitalization within 12 months)
- Use of acetaminophen (*this criteria only applies when the CGM version being used is older than the G6*)
- Use of long-acting insulin that is not Lantus or Tresiba
- For subjects who currently use a close-loop insulin pump and CGM: not being willing to turn off the closed-loop function
- Conditions that would make use of a CGM difficult (e.g., blindness, severe arthritis, immobility)
- Cystic fibrosis
- Current use of oral/inhaled glucocorticoids or other medications, which in the judgment of the investigator would be a contraindication to participation in the study
- Any other comorbidity that at the judgment of the investigator may interfere with the participation on the study (i.e. uncontrolled high blood pressure or thyr
Data sourced from ClinicalTrials.gov (NCT03676465). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.