Effect of Exercise on Insulin Resistance

Prediabetic State Clinical Trial

— EFFORT  

Official title:

Effect of Exercise on Insulin Resistance

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01941277
• Other study ID #: BSTE-0902
• Status: Terminated
• Phase: N/A
• Start date: August 2014
• Est. completion date: March 2015

Study information

• Verified date: December 2023
• Source: Abbott RDx Cardiometabolic
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effect of exercise on Insulin Resistance (IR) in subjects who do not routinely exercise and who are at risk of developing diabetes (prediabetes).

It is estimated that approximately 30-90 people will participate in this study at three study sites in the United States and United Kingdom.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 3
• Est. completion date: March 2015
• Est. primary completion date: March 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria

1. Aged 18 to 75 years.

2. Meets one of the three diagnostic criteria listed below (based on screening results or recorded result within one week of enrollment);

1. Fasting plasma or whole blood glucose (fasting defined as no caloric intake for at least 8 hours): 100 = 125 mg/dL (6.0-6.9 mmol/L)

2. HbA1c of 5.7% - 6.4% (39 - 46 mmol/mol)

3. 2-hour plasma glucose of 140-199 mg/dL (7.8-11.0 mmol/L) during an OGTT (as described by the WHO using a glucose load of 75 g anhydrous glucose dissolved in water)

3. No clinically significant adverse exercise response during the maximal graded exercise test

Exclusion Criteria

1. Weight loss diet program or weight change (>10%) within the past 6 months

2. Daily physical activity of >10,000 steps per day (as measured during the interval between visits 1 and 2)

3. Participates in deliberate structured exercise

4. Pregnant or intending to become pregnant

5. Cognitive or intellectual disability that prevents subject from providing informed consent or following protocol instructions.

6. Unwillingness to participate in all study procedures

7. Inability to give blood through multiple venous phlebotomies or to have an intravenous catheter

8. BMI greater than 40 kg/m2

9. Concurrent participation in another lifestyle modification trial

10. Diagnosis of diabetes based on any one of the following criteria:

1. Fasting plasma or whole blood glucose = 126 mg/dL (7 mmol/L)

2. HbA1c of >6.5% (>47 mmol/mol)

3. 2-hour plasma glucose = 200 mg/dL (11.1 mmol/L) during an OGTT

11. Any pre-existing or newly discovered medical condition that is deemed likely to put the subject at risk of injury during this trial. This may include but is not limited to:

1. Clinically relevant vascular or cerebrovascular event (e.g. stroke, recurrent transient ischemic attack (TIA), deep venous thrombosis or intracardiac thrombi, clinically significant edema within the previous 6 months

2. Current use of anti-psychotic, anti-convulsant, anti-coagulant, sedative medication, or cognition-enhancing medications

3. Current use of beta blockers (beta-adrenergic blocking agents)

4. Current or previous use (within the past year) of the following medications:

diabetes related medications or insulin; metformin; growth hormone; glucagon; dipeptidyl peptidase-4(DPP-4) inhibitors (saxagliptin, stigagliptin); glucagon-Like Peptide-1(GLP-1) mimetics (exenatide, liraglutide); sulfonylurea medication or other potential confounding medications

5. Medical conditon which predetermines insulin resistance (e.g. Marfan syndrome / severe Polycystic ovary syndrome (PCOS) / Cushing syndrome etc.).

6. Fasting triglycerides > 1000 mg/dL.

Related Conditions & MeSH terms

• Insulin Resistance
• Prediabetic State

Intervention

Behavioral:
• Current Recommendations Exercise Group

• Intensive Exercise Group

Locations

Country	Name	City	State
United Kingdom	Manchester University	Manchester
United Kingdom	Move Lab	Newcastle upon Tyne

Sponsors (1)

Lead Sponsor	Collaborator
Alere San Diego

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	A decrease in Insulin Resistance (IR) as measured by a change in IR.		change between baseline and 6 weeks