Influence of the Phases of the Menstrual Cycle on Glycemic Control When Performing Aerobic Exercise in Women With T1D

Diabetes Mellitus, Type 1 Clinical Trial

— TAILOR/1a  

Official title:

Influence of the Phases of the Menstrual Cycle on Glycemic Control Before, During, and After a Aerobic Exercise in Adult Women With Type 1 Diabetes (TAILOR/1a)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06086067
• Other study ID #: 1586990
• Status: Completed
• Phase: N/A
• Start date: September 15, 2023
• Est. completion date: February 1, 2024

Study information

• Verified date: April 2024
• Source: University of Valencia
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study corresponds to Task 8.1 of the project "Patient-tailored solutions for blood glucose control in type 1 diabetes- TAILOR" (PID2019-107722RB-C21).

It has been observed in different studies in healthy people that the glucose rate of appearance or disappearance during exercise is attenuated with the coincident rise in estrogen and progesterone during the mid-luteal phase of the menstrual cycle versus the early luteal phase.

The investigators hypothesize that in women with type 1 diabetes, glucose behavior when performing aerobic exercise may be different depending on the phase of the menstruation cycle. This analysis is necessary to improve physical exercise recommendations, both educational and technological, in women with type 1 diabetes, as well as improve the performance of artificial pancreas systems for automatic control of glucose levels under exercise in women.

Description:

This study will consist of two aerobic exercise sessions, one conducted at the beginning of the late follicular phase, where maximal estrogen concentration coincides with low progesterone levels, and the other session in the middle of the luteal phase, where peak values of estrogen and progesterone are generally observed.

Prior to the exercise sessions, an incremental exercise test will be performed to determine the working power in the cycle ergometer. At the beginning of the test, subjects will be sit quietly on the cycle ergometer for 3 min (0 W) before they will start the warm-up period of 3 min with cycling at a workload of 40 W. Then, the workload will increase by 20 W every minute until volitional exhaustion. Finally, 3 min active recovery at 40 W followed by 3 min passive recovery (0 W) will be conducted on the cycle ergometer. Lactate turn point 1 (LTP1) and maximum power (Pmax) will be determined in order to prescribe the exercise intensity.

The aerobic exercise session will begin with a 3 min resting period (sitting quietly on the cycle ergometer (0 W), followed by a 3 min warm-up at 40 W and a stepwise intensity increase by 20 W / min (to control for day-to-day variations in exercise response) until the 5% of Pmax from IET above PLTP1 is achieved (i.e. moderate steady state walking or low-intensity running or cycling). This target workload will be maintained for 30 min. Active and passive recovery periods of 3 min each will be the same as the incremental test.

To monitor the impact on blood glucose, blood draws will be performed at initial and every 10 minutes for aerobic sessions. A sample size of n=30 will be chosen.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: February 1, 2024
• Est. primary completion date: February 1, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 45 Years

Eligibility

Inclusion criteria:

• age between 18-45 years

• T1D with a diabetes duration for more than 2 years

• glycated hemoglobin (HbA1c) < 8.5% (<69 mmol mol-1)

• stable insulin regimen in the past 6 months with less than 20% change in total insulin daily dose

• multiple daily injections

• weekly physical activity of 90 min or more, but no practicing any sport as amateur or professional.

Exclusion Criteria:

-clinical conditions or use of medications (other than insulin) known to affect glycemic control (e.g., oral/parenteral steroids or metformin, among others).

Related Conditions & MeSH terms

• Diabetes Mellitus, Type 1

Intervention

Other:
• Aerobic session
This session will consist of an aerobic training session performed on a cycle ergometer.

Locations

Country	Name	City	State
Spain	Rodrigo Martin-San Agustin	Valencia

Sponsors (5)

Lead Sponsor	Collaborator
University of Valencia	Consorcio Centro de Investigación Biomédica en Red (CIBER), European Regional Development Fund, Ministerio de Ciencia e Innovación, Spain, Universitat Politècnica de València

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Blood glucose level	Blood glucose (mg/dL) will be measured through blood draws and YSI analysis	The evaluated time points for aerobic exercise will be at 20 and 10 minutes before the session, at the beginning of the training and at 10, 20, and 30 minutes during the interval, and at 10 and 20 minutes after finishing the training.
Primary	Mean interstitial glucose	Mean interstitial glucose (mg/dL) will be measured using the FreeStyle3 as a continuous glucose meter during 6 hours, 12 hours, and 24 hours before and after both exercise sessions.	24 hours pre-intervention and 24 hours post-intervention
Primary	Glycemic variability	Glycemic variability (measured using the Coefficient of Variation-CV) will be measured using the FreeStyle3 as a continuous glucose meter during 6 hours, 12 hours, and 24 hours before and after both exercise sessions.	24 hours pre-intervention and 24 hours post-intervention
Primary	Time spent at each glucose range	Time spent at each glucose range [euglycemia (70-180 mg/dL) or Time in range (TIR), level 1 or mild hypoglycemia (54-70 mg/dL), level 2 or severe hypoglycemia (<54 mg/dL), level 1 hyperglycemia (180-250 mg/dL) and level 2 hyperglycemia (>250 mg/dL)] will be measured using the FreeStyle3 as a continuous glucose meter during 6 hours, 12 hours, and 24 hours before and after both exercise sessions.	24 hours pre-intervention and 24 hours post-intervention
Secondary	Lactate	Lactate concentration (mmol/L) will be performed through blood extractions and measured using the YSI 2500.	pre-intervention and immediately after the intervention
Secondary	Oestrogens	estradiol levels (pg/ml) will be measured through blood extractions and subsequent analysis in the laboratory.	pre-intervention
Secondary	Progesterone	Progesterone (ng/mL) will be measured through blood extractions and subsequent analysis in the laboratory.	pre-intervention