T1D Closed-loop and Physical Activity

Diabetes type1 Clinical Trial

Official title:

"Impact of an Automated Closed-loop Insulin Infusion System on Adherence to Physical Activity in Patients With Type 1 Diabetes "

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06460558
• Other study ID #: 24Endocrino01
• Status: Recruiting
• Start date: May 6, 2024
• Est. completion date: May 6, 2026

Study information

• Verified date: May 2024
• Source: Centre Hospitalier Universitaire de Nice
• Contact: Nicolas CHEVALIER, MD
• Phone: 0492035519
• Email: chevalier.n[@]chu-nice.fr
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

"Physical activity is recognized as beneficial for patients living with type 1 diabetes (T1DM), with a demonstrated effect not only on HbA1c control [1] but also on reducing the incidence of diabetes-related complications [2,3]. It is recommended that patients living with T1DM perform 150 minutes of accumulated physical activity per week, without exceeding two consecutive days without physical activity [4]. Indeed, one meta-analysis reported that moderately vigorous activity (≥4.5 METs) was beneficial compared with lower-intensity activity, while three other studies noted that only vigorous physical activity (≥6 METs) predicted lower all-cause mortality rates [5]. However, T1DM can represent a major obstacle to physical activity because of the occurrence of fairly frequent hypoglycemia, including after physical effort, the need for early resugaring but also the risk of hyperglycemia (rebound or with certain activities) [6]. The advent of automated insulin delivery systems has led to a significant improvement in time on target and a reduction in the frequency of hypoglycemia, including during physical activity in some studies [7-9]. The aim of this study is therefore to evaluate, in a cohort of patients with T1DM, whether the implementation of a closed-loop automated insulin delivery system increases physical activity in patients with T1DM. Based on the interpretation of the ONAPS-PAQ [10], the investigator hypothesize that the implementation of the closed-loop system enables an individual to reach the 3000 MET/min/week threshold (considered ""Active+"" from this threshold onwards).

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 65
• Est. completion date: May 6, 2026
• Est. primary completion date: November 6, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Type 1 diabetes defined by clinical history and positive measurement of autoantibodies (anti-GAD or IA2), evolving for more than 6 months and treated by insulin pump for at least 6 months, for whom an indication for automated insulin delivery is retained, by criteria of glycemic control (HbA1c = 8% and/or significant glycemic variability and/or severe hypoglycemia) or poor quality of life, in accordance with reimbursement criteria validated by the CNAM for available systems.
• For women, existence of effective contraception (hormonal or mechanical) and no plans for pregnancy during the study period.
• Having a Health Care insurance."" "

Exclusion Criteria:

• Patient already involved in another experimental study
• Patient in a particular situation deemed incompatible with the study by the investigator
• Patient living in a department other than Alpes-Maritimes or Var
• Pregnant women
• Presence of a contraindication to physical activity
• Patient with linguistic or psychological incapacity to understand written information
• Patient refusing to give consent
• Patient deprived of liberty by administrative or judicial decision, under guardianship or trusteeship"" "

Related Conditions & MeSH terms

• Diabetes Mellitus, Type 1
• Diabetes type1

Intervention

Other:
• Type 1 diabetes with insulin infusion system
No intervention

Locations

Country	Name	City	State
France	CHU NiICE	Nice	Alpes Maritimes

Sponsors (1)

Lead Sponsor	Collaborator
Centre Hospitalier Universitaire de Nice

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	IPAQ score	"Measurement of IPAQ in METs/min/week (reflects the amount of physical activity practised using a validated questionnaire). There are seven items whose the result corresponds to the sum of the given figures. "	At the inclusion
Secondary	BAPAD-1 score "	The BAPAD-1 score, validated in French, will be used to assess the usual obstacles to physical activity in T1DM. It is a Likert scale (between 0-7) composed by twelve items. Then, a mean is calculated with all the answers.	At the inclusion
Secondary	BREQ-2	"To assess motivation to engage in physical activity, use the BREQ-2 score, validated by ONAPS. It is a Likert scale (between 0-7) composed by six items. Then, a mean is calculated with all the answers.	At the inclusion
Secondary	ONAPS PAQ	To assess sedentary behaviour, use the ONAPS PAQ score with only the sedentary behaviour section. 4 items. Then the sum of the results is calculated	At the inclusion