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Italian Diabetes and Exercise Study 2

Italian Diabetes and Exercise Study 2 - A Long-term Behavioural Intervention for Adoption and Maintenance of a Physically Active Lifestyle

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01600937
Acronym
IDES-2
Enrollment
300
Registered
2012-05-17
Start date
2012-10-31
Completion date
2017-02-28
Last updated
2017-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 Diabetes

Keywords

diabetes mellitus, diabetes education, behavioral therapy, behavior modification, physical activity, supervised exercise, physical fitness, HbA1c, modifiable cardiovascular risk factors, quality of life

Brief summary

Current guidelines recommend supervised mixed (aerobic+resistance) physical activity to ensure optimal benefits to control blood glucose, lipids, blood pressure, and other cardiovascular risk and to minimize injuries. However, these guidelines are difficult to put into action for a number of barriers and poor long-term patient compliance. This project will assess the effect of a behavioral intervention strategy on the promotion and maintenance of physical activity in type 2 diabetes.

Detailed description

An increasing prevalence of type 2 diabetes is associated with an aging population, a significant rise in the prevalence of obesity, and a sedentary lifestyle. In Italy, prevalence of diabetes is approximately 6%, with 90-95% of diabetic subjects having type 2. Strong evidence supports the importance of physical activity in the management of type 2 diabetes. However, current guidelines are difficult to put into action in this target population because of barriers and poor patient long-term compliance so it is difficult even identify the best strategies for physical activity behavior change. Existing studies employ small groups and clinically-based approaches with limited theoretical grounding for recommended health behavior change. Most fail to offer practical, sustainable, economically viable solutions, with documented long-term intervention efficacy. This study proposes to monitor any objective measurable changes in LTPA over a 3-year period after behavioral interventions (Physician recommendations for daily PA with and without supervised exercise training including individual theoretic & practical counseling). Hopefully, such behavioral intervention would offer a feasible procedure for long-term maintenance of physical activity and thus meet the call for a change of paradigm to move beyond the limited clinical focus by including theoretically population-based and real-life approaches for the management Type 2 Diabetes. After the selection for eligibility and a run-in period, patients will be randomized in two groups: 1) exercise (EXE) group receiving theoretical & practical exercise counseling including 2 sessions/ per wk for 1 month of supervised exercise training; and 2) control (CON) group receiving standard care including general physician recommendations for daily PA. Changes in physical activity behavior will be quantified using an accelerometer, in addition to a daily diary.

Interventions

BEHAVIORALTheoretical & practical exercise counseling

2 sessions/ per wk for 1 month

Sponsors

University of Roma La Sapienza
CollaboratorOTHER
Metabolic Fitness Association, Italy
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Type 2 diabetes 2. Age 40 to 80 years at screening 3. BMI \>27\<40 kg/m2 4. Sedentary for at least 6 months 5. Treated with prescribed diet and/or OHA and insulin 6. Able to walk for 1.6 Km unaided. 7. Eligible after positive outcome of cardiac evaluation

Exclusion criteria

1. All patients with a history of central nervous dysfunction such as hemiparesis, myelopathies, cerebral ataxia, significant musculoskeletal deformities such as an amputation, dysmetria or scoliosis, patients with movement abnormalities or arthritis limited by pain when exercising 2. A history of clinical evidence of severe cardiovascular disease which may limit or be a contraindication for exercise 3. Clinical evidence of vestibular dysfunction 4. Angina and related symptoms 5. Postural hypotension defined as a fall in arterial blood pressure when changing position of \>20 mmHg (systole) or \>10 mmHg (diastole 6. History of plantar sores

Design outcomes

Primary

MeasureTime frameDescription
Physical Activity Behavior3 yearsVolume of physical activity in METs-hr/wk; sedentary time; time spent in moderate-to-vigorous physical activity

Secondary

MeasureTime frameDescription
Physical fitness3 yearsPhysical fitness (Cardiorespiratory, fitness, muscle strength, hip and trunk flexibility)
Modifiable cardiovascular risk factors3 yearsModifiable cardiovascular risk factors (HbA1c, lipids, blood pressure, C-reactive protein, CHD 10-year risk scores)
Health related quality of life3 yearsQuality of life (Physical and mental SF-36 scores)
Musculo-skeletal disturbances3 yearsMusculo-skeletal symproms and scores

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026