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Effects of Exercise Intervention and Rehabilitation Exercise Intervention in Patients With Type 2 Diabetes

Effects of Exercise Intervention in Patients With Type 2 Diabetes - Strength Endurance Exercise Intervention Versus Combination of Strength Endurance Exercise Intervention and Rehabilitation Exercise Intervention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01393275
Enrollment
68
Registered
2011-07-13
Start date
2010-02-28
Completion date
2011-10-31
Last updated
2011-11-08

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

Conditions

Diabetes, Diabetes Mellitus, Non-Insulin-Dependent

Keywords

diabetes, exercise, intervention, rehabilitation, metabolic rate, sport

Brief summary

The purposes of the study are * to determine if a supervised exercise intervention is improving the metabolic parameters in type 2 diabetes patients * to investigate what kind of intervention (strength endurance training versus combined strength endurance training and rehabilitation exercise intervention)is more effective in improving the metabolic parameters in patients with type 2 diabetes * to assess which exercise intervention induces higher effects to the metabolic rate and cardiac and pulmonary capacity * to investigate what kind of intervention includes highest effects in long term persistence of these positive effects

Interventions

OTHERrehabilitation exercise intervention

exercise intervention: 15 minutes warm up, 30 minutes strength endurance training, 60 minutes rehabilitation exercise training - once a week 15 minutes warm up, 30 minutes strength endurance training - once a week

exercise intervention: 15 minutes warm up, 30 minutes strength endurance training, 5 minutes walking 55 minutes conversation in the group- once a week 15 minutes warm up, 30 minutes strength endurance training - once a week

Sponsors

Sportpark Zwickau, Germany
CollaboratorUNKNOWN
Sportpark Glauchau, Germany
CollaboratorUNKNOWN
Comenius University
CollaboratorOTHER
University of Giessen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* diagnosis of type 2 diabetes (ADA criteria) * admitted diabetes treatment will be diet and oral hypoglycemic agents

Exclusion criteria

* sports intervention \> 60 minutes per week medical conditions * proliferative retinopathy * instable coronary heart disease * acute clinically significant intercurrent disease * inability to perform scheduled physical activity programs

Design outcomes

Primary

MeasureTime frame
alteration of HbA1c-level (haemoglobin A1c)6 months

Secondary

MeasureTime frameDescription
alteration of LDL-cholesterol-level6 months
alteration of HDL-cholesterol-level6 months
alteration of triglyceride-level6 months
alteration of antidiabetic medications6 months
alteration of anthropometry6 monthsbody weight; body mass index; hip-to-waist-ratio
alteration of total cholesterol level6 months
alteration of resting metabolic rate6 months1. measured by Spirometrie (Cortex metamax) 2. calculated by Bio-impedance analysis (TANITA)
alteration of blood pressure6 months
alteration of cardiac and pulmonary capacity6 months1. measured by ergometry 2. six-minutes walk test
alteration of quality of life6 months
follow up of all parameters mentioned above15 monthsfollow up after 15 months without any supervised intervention
alteration of body composition6 monthsmeasured by Bio-impedance analysis

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026