NCT07509060Active, not recruiting
HCL in Adults With T1DM, Markedly Elevated HbA1c, and Psychological Vulnerability
The Impact of Introducing Hybrid Closed-loop Pump Therapy on Glucose Control, Quality of Life and Selected Chronic Complications in Type 1 Diabetes Patients With Chronically High Glucose Level and Psychological Problems
Source: ClinicalTrials.gov · Last updated 3 Apr 2026
Brief summary (registry, in English)
The objective of this study is to evaluate whether the mylife CamAPS FX hybrid closed loop (HCL) system improves glycemic control and quality of life in type 1 diabetes (T1DM) patients with a chronic lack of glycemic control and with psychological problems. After screening visit and run-in, patients will be randomized to treatment with mylife CamAPS FX HCL for 12 months (group I) or treatment with their current type of treatment for 3 months and mylife CamAPS FX HCL for next 9 months (group II). The HCL system used in the study will consist of mylife CamAPS FX controller, mylife YpsoPump insulin pump and Dexcom G6 continuous glucose monitoring system (CGM). Main inclusion criteria include: type 1 diabetes for at least 2 years, hemoglobin A1c (HbA1c) ≥ 9.0%, and psychological vulnerability. Primary glycemic outcomes include: differences between study groups in changes in time in range 70-180 mg/dL (TIR) and HbA1c after 3 months. Main secondary outcomes include: differences between groups in CGM-derived data after 3 months and within the entire cohort after 12 months, as well as changes within groups in psychological scores after 3 months and within the entire cohort after 12 months.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 30 (actual)
- First submitted
- 23 Mar 2026
- Start date
- Mar 2025
- Primary completion date
- Oct 2025
- Lead sponsor
- Jerzy Hohendorff
- Diseases
- Type 1 diabetes
- NCT number
- NCT07509060
What you commit to
- Study type: Interventional
- Participants enrolled: 30
- From Mar 2025 to the primary completion date, Oct 2025
- 3 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Current treatment with hybrid closed loop system.
Other illness
- Known or suspected contact allergy to the pump cannula or adhesives.
- Renal impairment on dialysis.
- Known severe mental disorders (schizophrenia, psychotic episodes, bipolar disorder, dementia, drugs and alcohol abuse, eating disorders - anorexia, bulimia, learning disabilities, depression with active suicidal ideation) which are likely to interfere with the normal conduct of the study and interpretation of the study results as judged by the investigator.
Lab values
- Current treatment with drugs known to interfere with glucose metabolism, e.g. systemic corticosteroids.
Other
- Daily dose of insulin \>300 IU.
- Pregnancy or planning pregnancy, breast feeding.
- Proliferative, uncontrolled retinopathy.
- Patients not able to follow study instructions as judged by the investigator
Who the study is looking for
- Age 18 - 65 years at time of screening
- A clinical diagnosis of type 1 diabetes for 2 years or more as determined by the medical record or other source documentation by a health care professional qualified to make a diagnosis.
- HbA1c of \>= 9.0% in last 6 months.
- Multiple daily injections or insulin pump therapy with or without CGM, except HCL
- Total daily insulin 5 U/day - 300 U/day
- Adequate hearing to hear alarms and adequate vision to view display
- Willing to follow study specific instructions and improve glucose control.
- Willing to use CamAPS FX continuously throughout the study.
- Female participants of child-bearing age should be on effective contraception and must have a negative urine-HCG pregnancy test at screening
- Psychological problems defined as one of the following:
- Diabetes Distress Scale (DDS-17) - assesses diabetes-specific emotional distress across four domains: Emotional Burden, Physician-Related Distress, Regimen-Related Distress, and Interpersonal Distress. Scale: 1- 6. Scores ≥2.0 indicate moderate distress.
- Problem Areas in Diabetes (PAID) Scale - measures overall emotional burden related to diabetes. Scale: 0-100. Total scores ≥40 indicate clinically significant diabetes distress.
- Diabetes Burnout Questionnaire (DBQ) - evaluates emotional exhaustion, detachment from diabetes care, and perceived loss of control. Scale: 1-5. Scores \>2 suggest clinically relevant burnout symptoms.
- Quick Inventory of Depressive Symptomatology (QIDS) - assesses depressive symptoms over the previous week. Scale: 0-27. Scores ≥6 are considered indicative of clinically relevant depressive symptoms, with higher score ranges reflecting increasing symptom severity.
- Patient Health Questionnaire-9 (PHQ-9) - assesses depressive symptoms over the preceding two weeks. Scale: 0-27. Scores ≥10 indicate clinically relevant depression.
- WHO-5 Well-Being Index - measures positive well-being. Scale: 0-25. Scores ≤13 indicate reduced well-being.
- Hypoglycaemia Fear Survey (HFS-II) - assesses behaviours and concerns related to hypoglycaemia; in the Polish version of the Hypoglycaemia Fear Survey-II. Scale: 0-132. Scores above 40 are commonly used to indicate elevated fear of hypoglycaemia.
- EQ-5D-5L (EuroQol Group, 2011) - evaluates health-related quality of life across five dimensions and includes a visual analogue scale (VAS 0-100), values below 50 considered indicative of markedly reduced perceived health status.
- Symptom Questionnaire (KO "0") - used to assess anxiety-related psychological symptoms. Scale: 0-336. Scores above normative thresholds (180 for males, 200 for females) indicate clinically relevant anxiety symptomatology.
Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers
Sites (3)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Medical University of Silesia in Katowice, Poland Coordinator of this site? Confirm its status | Katowice | Poland | Unknown status |
| University Hospital in Krakow Coordinator of this site? Confirm its status | Krakow | Poland | Unknown status |
| Poznan University of Medical Science, Poland Coordinator of this site? Confirm its status | Poznan | Poland | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.