Diabetes Mellitus, Type 1 Clinical Trial
Official title:
Impact of Insulin Detemir Versus Insulin Glargine on Glycaemic Control and Metabolism During Exercise in Type 1 Diabetes
Exercise is an important part of a healthy lifestyle, and many people with Type 1 Diabetes
like to take part in regular sport and exercise. The majority of people with Type 1 Diabetes
are treated with a "basal bolus" insulin regimen, with background insulin provided by
long-acting "basal" insulin doses, and "bolus" doses of short-acting insulin used to
accompany food intake. Evidence shows that the main factor preventing people with diabetes
from pursuing a more active lifestyle is fear of low blood glucose (hypoglycaemia). A
previous study has shown that the type of background insulin affects the likelihood of an
individual suffering hypoglycaemia during exercise and for 2 and a half hours afterwards.
The aim of this study is to examine this further.
The two most commonly used long-acting insulins, insulin glargine and insulin detemir, will
be compared. Previous data suggests that there is a greater likelihood of hypoglycaemia with
insulin glargine than insulin detemir. Exercise intensity can have an influence on the
likelihood of hypoglycaemia, and in this previous study exercise intensity was measured
using heart rate. This study will use a more formal definition of exercise intensity. The
investigators will study blood glucose during exercise, but also metabolism as measured by
hormones affecting blood glucose levels as well as markers of fat metabolism. The
investigators will also use a continuous glucose monitoring system (CGMS) to consider
hypoglycaemia on thei night following exercise as this is a recognised consequence of
exercise in type 1 diabetes.
The null hypothesis to be tested in this study is that there is no difference between the
two insulins in their effect on blood glucose levels and metabolism during exercise and
rates of nocturnal hypoglycaemia after exercise.
A1: At the first appointment, potential participants will be screened regarding the
inclusion criteria, and if eligible to take part the study information sheet will be
discussed with them in detail. Written, informed consent will be obtained if participants
are willing to take part in the study. Participants will be given advice and support from
this point in order to optimise basal insulin therapy using their usual basal insulin.
A2: Following a period of at least 3 weeks from recruitment into the study, participants
will have their maximal oxygen uptake (VO2 MAX - a measure of capacity for physical
exercise) assessed.
A3: After at least 4 weeks following recruitment , to allow time for optimisation of basal
insulin therapy, and at least one week following A2, the participant's metabolism will then
be assessed during and after 60 minutes of exercise at 50% VO2 MAX. Participants will be
fitted with a continuous glucose monitoring system (CGMS) to monitor glucose levels for the
24 hours after exercise finishes.
A4: At least 24 hours and no more than 7 days after A3 the participant will switched to
using the other trial insulin for basal insulin therapy. Again, participants will be
provided with advice and support in order to optimise treatment.
A5: At least 4 weeks following A4, the participant's metabolism will once again be assessed
during and after 60 minutes of exercise at 50% VO2 MAX. Participants will again be fitted
with CGMS to monitor glucose levels for the 24 hours after exercise finishes.
A6: Once the 24 hours after exercise are complete, the study finishes and participants
re-start their usual basal insulin.
;
Allocation: Non-Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
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