Skip to main content
Clinical Trials/NCT01289587
NCT01289587
Completed
N/A

Efficacy and Feasibility of a Program to Promote Physical Activity in Patients With Type 2 Diabetes (DIAfit)

University of Lausanne Hospitals1 site in 1 country185 target enrollmentFebruary 2011
ConditionsDiabetes

Overview

Phase
N/A
Intervention
Not specified
Conditions
Diabetes
Sponsor
University of Lausanne Hospitals
Enrollment
185
Locations
1
Primary Endpoint
Aerobic fitness
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The aim of this study is to evaluate the effects of a physical activity intervention in patients with type 2 diabetes in a community setting.

Detailed Description

The aim of this study is 1. to evaluate the effects (before and after) of a physical activity program (DIAfit program) which contains 36 sessions of structured PA and also encourages unstructured PA in an unselected population of patients with type 2 diabetes independent of the selected variant of the program 2. to compare the effects of a standard DIAfit program (3 times per week for 12 weeks) with and alternative program which suggests a more progressive PA activity intensity (starting with one PA session per week during 4 weeks and then twice a week over a period of 16 more weeks (20 weeks total). In total the program also consist of 36 sessions)

Registry
clinicaltrials.gov
Start Date
February 2011
End Date
October 2017
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of Lausanne Hospitals
Responsible Party
Principal Investigator
Principal Investigator

Jardena Puder

MD

University of Lausanne Hospitals

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of type 2 diabetes

Exclusion Criteria

  • Orthopedic complications
  • Diabetic foot ulceration
  • "Active " cardiac (ischemia during the exercise test) or stade III peripheral vascular disease
  • Untreated proliferative retinopathy
  • Autonomic neuropathy
  • Active psychiatric, neurological, orthopedic, muscular or rheumatic disease interfering with a participation in a physical activity program
  • Pregnancy

Outcomes

Primary Outcomes

Aerobic fitness

Time Frame: End of the intervention (36 PA sessions, 12 vs 20 weeks depending on assignment)

Change in aerobic fitness

Secondary Outcomes

  • Body composition(At the end of the intervention (36 PA sessions, 12 vs 20 weeks depending on assignment))
  • Lipid values(At the end of the intervention (36 PA sessions, 12 vs 20 weeks depending on assignment))
  • Qualitative evaluation (satisfaction of achievement of personal objectives, evaluation of group session)(At the end of the intervention (36 PA sessions, 12 vs 20 weeks depending on assignment))
  • Adherence/Attendance: Number of physical activity sessions attended(During the intervention)
  • Self-efficacy(At the end of the intervention (36 PA sessions, 12 vs 20 weeks depending on assignment))
  • HbA1c(At the end of the intervention (36 PA sessions, 12 vs 20 weeks depending on assignment))
  • Physical activity(At the end of the intervention (36 PA sessions, 12 vs 20 weeks depending on assignment))
  • Motor performance(At the end of the intervention (36 PA sessions, 12 vs 20 weeks depending on assignment))
  • BMI(At the end of the intervention (36 PA sessions, 12 vs 20 weeks depending on assignment))
  • Well-being(At the end of the intervention (36 PA sessions, 12 vs 20 weeks depending on assignment))

Study Sites (1)

Loading locations...

Similar Trials