Need-driven Treatment of the Patients With Type 1 Diabetes

NCT ID: NCT07128992

Last Updated: 2025-08-19

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Total Enrollment: 125 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2025-10-06
• Study Completion Date: 2028-12-31

Brief Summary

This prospective study evaluates the safety of extending the interval of routine calendar-based follow-up visits from every 12 months to every 24 months in patients with type 1 diabetes who are in good glycemic control and suitable for remote monitoring. The primary outcome is the proportion of patients who maintain good glycemic control during the 24-month follow-up period.

Participants will attend two in-person visits at baseline (month 0) and at the end of follow-up (month 24), which include a comprehensive clinical examination, assessment of glucose control, and laboratory testing. One remote contact will occur at month 12 for prescription renewal and review of glucose data. Patients may contact their care unit as needed throughout the study. At the baseline and final visits, participants will complete a questionnaire assessing their perceived ability to manage self-care, the safety of the care plan, and their ability to contact their care provider when necessary.

Detailed Description

The primary outcome of this study is the proportion of patients who maintain good glycemic control during the 24-month follow-up period. A clinically significant result is defined as no more than 14% of patients (95% confidence interval: 8%-20%) experiencing deterioration in glucose control, indicated by Time in Range (TIR) < 70% or HbA1c > 53 mmol/mol. If at least 125 patients are enrolled, need-based care can be demonstrated to be safe.

The study also evaluates the performance and safety of the "MD Diabetes Huolijono" software application, which issues alerts to healthcare professionals if glucose control worsens or if the patient is hospitalized. Between visits, patients using a Libre sensor with multiple daily insulin injections will be monitored using the MD Diabetes Huolijono system, while other patients will continue standard self-monitoring.

Healthcare contact data will be retrieved from the data service for each participant for the 24 months prior to study enrollment and throughout the follow-up period.

Conditions

Type 1 Diabetes (T1D); Glucose Control

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Adults (≥18 years) with type1 diabetes under the care of the Pirkanmaa Wellbeing Service

Eligible participants are patients with type 1 diabetes who use continuous glucose monitoring systems, have no complications or other conditions requiring frequent hospital or outpatient care, and are in good glycemic control (HbA1c \< 53 mmol/mol, TIR \> 70%, TBR \< 4%, TAR \> 25%).

Control visit interval

Intervention Type: OTHER

Study investigates whether it is safe to extend the interval of routine calendar-based follow-up visits from every 12 to every 24 months in patients with type 1 diabetes.

Interventions

Control visit interval

Study investigates whether it is safe to extend the interval of routine calendar-based follow-up visits from every 12 to every 24 months in patients with type 1 diabetes.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Age ≥ 18 years
• Diagnosis of type 1 diabetes
• Treatment with multiple daily injections or insulin pump therapy
• Duration of diabetes ≥ 1 year
• Good glycemic control over the previous two weeks, defined as:
• HbA1c < 53 mmol/mol
• Time in Range (TIR) > 70%
• Time Below Range (TBR) < 4%
• Time Above Range (TAR) < 25%
• Use of a continuous glucose monitoring system connected via a smartphone application
• Under specialist diabetes care within the Pirkanmaa Wellbeing Services County (Pirha)
• Willing to accept remote diabetes care by granting the diabetes team at Tampere University Hospital access to glucose data
• No need for regular specialist care due to other medical conditions
• Provides informed consent to participate in the study

Exclusion Criteria

• Age < 18 years
• Duration of diabetes < 1 year
• Pregnancy
• Not using multiple daily injections or insulin pump therapy
• Not using a continuous glucose monitoring system
• Does not accept remote care
• History of diabetic ketoacidosis or severe hypoglycemia within the past 12 months
• Presence of retinopathy
• No retinal imaging performed within the past 12 months
• Urine albumin-creatinine ratio (uACR) > 3 mg/mmol or estimated glomerular filtration rate (eGFR) < 60 ml/min/1.73 m² on two occasions over a period of more than 3 months
• Undergoing dialysis or post-kidney transplantation
• Cardiovascular disease (excluding hypertension)
• Neuropathy, foot ulcer, or amputation (foot risk category 1-3)
• Scheduled hospital outpatient visits for other specialties within the next 12 months
• Not under specialist diabetes care within the Pirkanmaa Wellbeing Services County (Pirha)

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Tampere University Hospital

OTHER

Sponsor Role: lead

Responsible Party

Saara Metso

Head of the unit of endocrinology, Associate professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Saara Metso, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Tampere University Hospital, Pirkanmaa Wellbeing County

Central Contacts

Saara E Metso, MD, PhD

Role: CONTACT

saara.metso@pirha.fi

+358405310154

Päivi Hannula, MD, PhD

Role: CONTACT

paivi.hannula@pirha.fi

+358331164402

Other Identifiers

T67674

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

R25006L

Identifier Type: -

Identifier Source: org_study_id