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The Finnish Diabetes Prevention Study (DPS)

F

Finnish Institute for Health and Welfare

Status

Active, not recruiting

Conditions

Type 2 Diabetes

Treatments

Behavioral: Intensive lifestyle counselling

Study type

Interventional

Funder types

Other

Identifiers

NCT00518167
KTL151-6

Details and patient eligibility

About

The aim of this study is to clarify whether lifestyle intervention provided to people with high type 2 diabetes risk will lower the cumulative incidence of diabetes. Furthermore, the aim is to study the effect of lifestyle intervention on cardiovascular risk.

Enrollment

522 patients

Sex

All

Ages

40 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • impaired glucose tolerance (p-glucose 2 hours after a 75 g oral glucose load between 7.8 and 11.0 mmol/l)
  • body mass index 25 or higher

Exclusion criteria

  • diabetes (previous gestational diabetes accepted)
  • other chronic disease rendering survival for 6 years
  • condition or medication affecting glucose tolerance
  • recent myocardial infarction

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

522 participants in 2 patient groups

1
Experimental group
Description:
Intensive lifestyle intervention
Treatment:
Behavioral: Intensive lifestyle counselling
2
No Intervention group
Description:
Standard counselling at baseline

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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