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Identifying the Effect and Working Mechanisms of MyPlan 2.0 in Adults With Type 2 Diabetes

U

University Ghent

Status

Completed

Conditions

Chronic Disease

Treatments

Behavioral: MyPlan 2.0

Study type

Interventional

Funder types

Other

Identifiers

NCT03291171
MyPlan2.0_diabetes

Details and patient eligibility

About

The aim of this study is to investigate whether and how 'MyPlan 2.0' helps adults with type 2 diabetes to be more physically active or less sedentary. Two groups will be created, an intervention group and a waiting-list control group.

Full description

The aim of this study is to investigate whether and how 'MyPlan 2.0' helps adults with type 2 diabetes to be more physically active or less sedentary. Two groups will be created, an intervention group and a waiting-list control group. Both groups will be tested during three testing waves: pretest, posttest and follow-up test. Only the intervention group will be given acces to 'MyPlan 2.0'. 'MyPlan 2.0' consists of a website and mobile application targeting physical activity and sedentary behaviour. The intervention has a duration of five weeks.

Enrollment

56 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years or older
  • Type 2 diabetes
  • Have access to internet
  • Being computer literate

Exclusion criteria

  • not Dutch Speaking

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

56 participants in 2 patient groups

Intervention group
Experimental group
Description:
Participants will receive the e- and mHealth intervention 'MyPlan 2.0'.
Treatment:
Behavioral: MyPlan 2.0
Waiting-list control group
No Intervention group
Description:
Participants will not receive the e- and mHealth intervention 'MyPlan 2.0', but will be given access to the intervention after all testing phases.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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