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Effect of Mental Stress on Glucose Control in Patients With Diabetes Mellitus (EMSOD)

Primary Purpose

Diabetes Mellitus, Mental Stress

Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
stress
Sponsored by
University Hospital, Basel, Switzerland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Diabetes Mellitus

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • diabetes mellitus type 1 and type 2
  • stable glucose control
  • valid driver license
  • written informed consent

Exclusion Criteria:

  • pregnancy
  • unstable coronary artery disease
  • limited visual acuity or unstable proliferative diabetic retinopathy
  • uncontrolled hypertension (BP >160/95mmHg).

Sites / Locations

  • Kantonsspital Frauenfeld

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Stress

Arm Description

Outcomes

Primary Outcome Measures

Mean and maximum change from baseline in glucose level (mmol/l)
Glucose level will be measured before and every 15-30 minutes after stress application for up to 240 minutes

Secondary Outcome Measures

Full Information

First Posted
July 12, 2011
Last Updated
February 28, 2012
Sponsor
University Hospital, Basel, Switzerland
Collaborators
Kantonsspital Frauenfeld
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1. Study Identification

Unique Protocol Identification Number
NCT01396330
Brief Title
Effect of Mental Stress on Glucose Control in Patients With Diabetes Mellitus
Acronym
EMSOD
Official Title
Effect of Prolonged Mental Stress During Safe Driving Training Courses on Glucose Control in Patients With Diabetes Mellitus Type 2
Study Type
Interventional

2. Study Status

Record Verification Date
February 2012
Overall Recruitment Status
Completed
Study Start Date
September 2011 (undefined)
Primary Completion Date
November 2011 (Actual)
Study Completion Date
November 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital, Basel, Switzerland
Collaborators
Kantonsspital Frauenfeld

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Introduction Stress is part of the investigators daily life, and means to cope with it allow adaptation and survival. To this end, physiological pathways are activated, including neuroendocrine, cardiovascular and metabolic responses. In short term, the majority of consequences are beneficial, in the long run, however, chronic psychosocial stress may constitute an increased risk for coronary heart disease, type 2 diabetes, and disability. Acute mental stress induces an exaggerated release of stress hormones e.g. catecholamine and cortisol which are thought not only to increase heart rate (HR) and blood pressure (BP) but also to increase blood glucose levels. In clinical practice, patients and health care providers are often confronted with questions concerning psychological stress as a possible reason for glucose fluctuations. Whether stress itself or poor treatment adherence is responsible for the altered glucose control remains often controversial. Differences in the inter- and intraindividual response to stress have been suggested, but only a few small studies have addressed the effect of acute psychological stress on glucose control in patients with diabetes. Patients with type 2 diabetes may overestimate the effect of acute psychological stress on glucose control but further studies are clearly needed to definitely exclude or confirm a relevant effect of stress on the glucose control in diabetic patients. For example, effects of longer lasting or repetitive events of psychological stress on glucose concentrations still remain elusive. The aim of the present study was therefore to investigate the effect of prolonged psychological stress by means of repetitive safe driving training courses on glucose control in patients with diabetes. Patients and Methods Forty patients with type 1 or insulin-treated type 2 diabetes attending the outpatient-clinic of the Kantonsspital Frauenfeld or University Hospital of Zurich for regular visits are invited to participate. Included are patients on any oral glucose-lowering treatment and at least one daily injection of insulin, a valid driver license and written informed consent given. Exclusion criteria are diabetes duration <2 years, pregnancy, unstable coronary artery disease, limited visual acuity or unstable proliferative diabetic retinopathy, uncontrolled hypertension (BP >160/95mmHg) and pituitary or adrenal disease. The Ethics committee of the Kanton Thurgau approved the protocol and the study conform to the principles outlined in the Declaration of Helsinki. Study protocol Each patient completes a control and a stress testing day which takes place consecutively in a randomized order. Randomization is performed by an uninvolved third person. The study is carried out at the driving training area of the Touring Club Switzerland at Hinwil. Patients are advised to have lunch before 12:00 a.m. and to abstain from food thenceforth. Drinking mineral water remains allowed during the entire study days, and the patients have to take their basal insulin and other medication as usual. Patients are advised to arrive at the driving training area between 2:30 and 3:00 p.m. At arrival, a capillary glucose measurement is carried out, and glucose concentrations ≥10mmol/l are corrected with short-acting insulin analogues (glucose target 6 - 8mmol/l). Subsequently, no additional adjustment with insulin is allowed during the study. Glucose concentrations ≤4mmol/l are always corrected with administration of 10g carbohydrate (DextroEnergy® or orange juice). On both study days, patients ingest a standard meal at 4:45 p.m. (i.e. 15min before the driving training). Immediately after the meal, short-acting insulin is injected in knowledge of the carbohydrate content (same dose on both days) or oral antidiabetics are ingested as usual. Measurements of capillary and plasma glucose concentration, blood pressure, heart rate, stress perception and salivary cortisol concentration are carried out in regular intervals between 4 and 9 p.m. on both study days. On the control day, patients are placed in a quiet room and are permitted to read. They also have the possibility to leave the room and stay on a balcony. On the stress testing day, patients complete a driving training with their car between 5 and 7 p.m. The driving training consists of 3 consecutive exercises: first, a slalom track on dry and wet asphalt, secondly, a full braking exercise with water obstacles. Thirdly, the car is hurled around by a mechanical plate and the patients has to regain control over it.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Mental Stress

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Stress
Arm Type
Other
Intervention Type
Behavioral
Intervention Name(s)
stress
Intervention Description
3 professional safe drive training courses each lasting 30 minutes
Primary Outcome Measure Information:
Title
Mean and maximum change from baseline in glucose level (mmol/l)
Description
Glucose level will be measured before and every 15-30 minutes after stress application for up to 240 minutes
Time Frame
within 240 minutes after stress

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: diabetes mellitus type 1 and type 2 stable glucose control valid driver license written informed consent Exclusion Criteria: pregnancy unstable coronary artery disease limited visual acuity or unstable proliferative diabetic retinopathy uncontrolled hypertension (BP >160/95mmHg).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Wiesli, MD
Organizational Affiliation
Kantonsspital Frauenfeld
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Heiko Uthoff, MD
Organizational Affiliation
University Hospital, Basel, Switzerland
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kantonsspital Frauenfeld
City
Frauenfeld
ZIP/Postal Code
8501
Country
Switzerland

12. IPD Sharing Statement

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Effect of Mental Stress on Glucose Control in Patients With Diabetes Mellitus

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