Overview

This trial is active, not recruiting.

Condition hypoglycemia
Treatments aerobic exercise, resistance exercise
Sponsor Oregon Health and Science University
Start date February 2016
End date September 2016
Trial size 14 participants
Trial identifier NCT02687893, 15228

Summary

Growing evidence provided by many observational studies has established a strong link between decreased sleep duration and poor glucoregulation. Sleep deprivation and poor sleep quality induce insulin resistance and decrease glucose tolerance in healthy individuals. However, the influence of poor sleep quality on glycemic control of patients with Type 1 diabetes mellitus (T1DM) is unknown. Persistent sleep deprivation among patients with T1DM has been reported, and this sleep loss can be attributed in part to nocturnal hypoglycemia. Nocturnal iatrogenic hypoglycemia is a limitation of current intensive insulin therapies. Although severe hypoglycemia is associated with adverse events such as seizures and death, less severe nocturnal hypoglycemia has been linked to broad range of adverse consequences, both acutely and long term. Hypoglycemia stimulates the sympathetic nervous system as a stress response, leading to the stimulation of the hypothalamic-pituitary-adrenal axis (HPA). This results in a counter regulatory hormone cascade, which elicits an excessive cortisol secretion, which is known to cause sleep disturbance and could impair glucose homeostasis after the hypoglycemic event. The hyperinsulinemia in T1DM patients promotes HPA hyperactivity as well, which is also associated with impaired sleep quality by leading to sleep fragmentation, decreased slow wave sleep and shortened sleep duration. Sleep disturbances due to nocturnal hypoglycemia can exacerbate HPA axis dysfunction, adversely affecting the sleep-wake cycle.

The goal of the study is to understand the impact of nocturnal hypoglycemia on sleep.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification safety/efficacy study
Intervention model crossover assignment
Masking open label
Primary purpose treatment
Arm
(Experimental)
Subjects will complete 45 minutes of aerobic exercise twice during a 7 day period. Exercise will be graded based on the participant's relative capacity determined at the screening visit. Each exercise session will be followed by 60 minutes of monitored resting recovery.
aerobic exercise
Subjects will exercise on a treadmill for 45 minutes twice during the intervention week. Subjects will exercise at a fixed intensity level to a target heart rate (±10%) based on the heart rate achieved at 60% of their VO2max determined at screening. The speed and grade of the treadmill will be adjusted by trained research personnel with a goal of keeping participants within their target heart rate range for the entire 45 minutes.
(Experimental)
Subjects will complete 45 minutes of anaerobic exercise twice during a 7 day period. Each exercise session will be followed by 60 minutes of monitored resting recovery.
resistance exercise
Subjects will participate in resistance exercises for 45 minutes twice during the intervention week. Subjects will perform multiple-joint exercises with slow to moderate lifting velocity, for 1-3 sets per exercise at a weight that can be lifted for 8-12 repetitions (~60-80% of 1-repetition max). The exercises may include leg press, bench press, leg extension, leg flexion and seated row. Subjects will perform the exercises through the full range of motion. Between each set of repetitions, there would be a 2 minute rest period. The duration of the exercise testing would be approximately 45 minutes.
(No Intervention)
Subjects will perform no exercise during this week.

Primary Outcomes

Measure
Mean duration of time with sensed glucose less than 70 mg/dl post-exercise
time frame: 16 hours

Secondary Outcomes

Measure
Mean duration with sensed glucose between 70 - 180 mg/dl post-exercise
time frame: 16 hours
Mean duration with capillary blood glucose between 70 - 180 mg/dl
time frame: 4 weeks
Mean wake up after sleep onset duration post-exercise
time frame: 16 hours
Mean amplitude of glucose excursions
time frame: 4 weeks
Mean duration of total sleep time
time frame: 4 weeks
Mean time subject in bed
time frame: 4 weeks
Mean time for sleep onset
time frame: 4 weeks
Mean time of sleep efficiency
time frame: 4 weeks
Mean number of wake bouts
time frame: 4 weeks
Mean wake bout time
time frame: 4 weeks
Mean number of sleep bouts
time frame: 4 weeks
Mean sleep bout time
time frame: 4 weeks
Mean number of carbohydrate treatments to treat hypoglycemia
time frame: 4 weeks
Mean daily carbohydrate intake
time frame: 4 weeks
Mean daily insulin intake
time frame: 4 weeks
Mean of total duration of activity by the subject
time frame: 4 weeks
Mean duration of time with sensed glucose < 50 mg/dl
time frame: 4 weeks
Mean duration of time with capillary blood glucose < 50 mg/dl
time frame: 4 weeks
Mean duration of time with capillary blood glucose < 70 mg/dl
time frame: 4 weeks
Mean duration of time with sensed glucose > 180 mg/dl
time frame: 4 weeks
Mean duration of time with capillary blood glucose > 180 mg/dl
time frame: 4 weeks

Eligibility Criteria

Male or female participants from 21 years up to 45 years old.

Inclusion Criteria: 1. Diagnosis of type 1 diabetes mellitus for at least 1 year. 2. Male or female subjects 21 to 45 years of age. 3. Physically active on a regular basis, i.e. at least 3 days of physical activity per week. 4. Physically willing and able to perform 45 min of exercise (as determined by the investigator after reviewing the subjects activity level) 5. Current use of an insulin pump. 6. Willingness to follow all study procedures, including attending all clinic visits. 7. Willingness to sign informed consent and HIPAA documents. Exclusion Criteria: 1. Female of childbearing potential who is pregnant or intending to become pregnant or breast-feeding, or is not using adequate contraceptive methods. Acceptable contraception includes birth control pill / patch / vaginal ring, Depo-Provera, Norplant, an intrauterine device (IUD), the double barrier method (the woman uses a diaphragm and spermicide and the man uses a condom), or abstinence. 2. Any cardiovascular disease, defined as a clinically significant EKG abnormality at the time of screening or any history of: stroke, heart failure, myocardial infarction, angina pectoris, or coronary arterial bypass graft or angioplasty. Diagnosis of 2nd or 3rd degree heart block or any non-physiological arrhythmia judged by the investigator to be exclusionary. 3. Renal insufficiency (GFR < 60 ml/min, using the MDRD equation as report by the OHSU laboratory). 4. Impaired liver function, defined as AST or ALT ≥2.5 times upper limit of normal, according to OHSU laboratory reference ranges. 5. Hematocrit of less than or equal to 34%. 6. History of severe hypoglycemia during the past 12 months prior to screening visit or hypoglycemia unawareness as judged by the investigator. 7. Adrenal insufficiency. 8. Any active infection. 9. Known or suspected abuse of alcohol, narcotics, or illicit drugs (except marijuana use). 10. Seizure disorder. 11. Active foot ulceration. 12. Severe peripheral arterial disease characterized by ischemic rest pain or severe claudication. 13. Major surgical operation within 30 days prior to screening. 14. Use of an investigational drug within 30 days prior to screening. 15. Chronic usage of any immunosuppressive medication (such as cyclosporine, azathioprine, sirolimus, or tacrolimus). 16. Bleeding disorder, treatment with warfarin, or platelet count below 50,000. 17. Insulin resistance requiring more than 200 units per day. 18. Need for uninterrupted treatment with acetaminophen. 19. Current administration of oral or parenteral corticosteroids. 20. Any life threatening disease, including malignant neoplasms and medical history of malignant neoplasms within the past 5 years prior to screening (except basal and squamous cell skin cancer). 21. C peptide level of ≥0.5 ng/ml 22. Any concurrent illness, other than diabetes, that is not controlled by a stable therapeutic regimen. 23. Beta blockers or non-dihydropyridine calcium channel blockers. 24. A positive response to any of the questions from the Physical Activity Readiness Questionnaire. 25. Any chest discomfort with physical activity, including pain or pressure, or other types of discomfort. 26. Any clinically significant disease or disorder which in the opinion of the Investigator may jeopardize the subject's safety or compliance with the protocol.

Additional Information

Official title A Randomized, Three-way, Cross-over Study to Assess the Impact of Nocturnal Hypoglycemia on Sleep in Patients With Type 1 Diabetes
Principal investigator Peter G Jacobs, PhD
Description The study duration is 4 weeks long, during which subjects will undergo a 1 week run-in period followed by 3 randomized weeks of observational study. During the 1 week run-in period, subjects will familiarize themselves with the CGM and the other data collection procedures. Following the run-in week, the subject will be randomized to a specific order of observation weeks. The three observation weeks are a resistance training week, an aerobic exercise week and a control week with no explicit exercise. During the observation weeks, there will be 4 interventions planned, two during both the aerobic exercise and the resistance training week. See Schematic below for details. During both the aerobic exercise week intervention visits, subjects will exercise for ~45 minutes on a treadmill and during the resistance training week, subjects will perform strength training exercises for 1-3 sets per exercise at a weight that can be lifted for 8-12 repetitions (~60-80% of 1-repetition max). The duration of the resistance training period is expected to be ~45min. Subjects will continue to perform daily activities during each of the weeks. During each week, the subject will wear one subcutaneous DexcomTM G4 or DexcomTM G4 Share continuous glucose monitoring (CGM) system, one activity monitor- ActiGraph wGT3X-BT or ActiGraph GT9X, one insulin pump (subject's own pump) and one Samsung Galaxy S4 phone loaded with two applications- meal memory and moves. The CGM system will provide sensed glucose data every 5 minutes. The CGM data will be blinded to the patient to prevent any abrupt changes in behavior. The accuracy of the sensed data will be obtained by reference measurements of capillary blood glucose. The activity monitor will be secured on the dominant wrist and uses an accelerometer to collect movement data at a high frequency (80Hz). The activity monitor measures both motion and ambient light, this data would be used to determine the various sleep quality measures. The subject's insulin dosage information from the pump will be downloaded for data analysis purposes. The subject's daily meal intake (photographic log and note diary) and daily movement pattern information will be downloaded from the phone. During the 4 exercise intervention visits, subject's heart rate, accelerometry information from the torso and oxygen consumption measured breath by breath may be collected for data analysis purposes.
Trial information was received from ClinicalTrials.gov and was last updated in September 2016.
Information provided to ClinicalTrials.gov by Oregon Health and Science University.