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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Intervention group | Experimental | Participants will receive the e- and mHealth intervention 'MyPlan 2.0'. |
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| Waiting-list control group | No Intervention | Participants will not receive the e- and mHealth intervention 'MyPlan 2.0', but will be given access to the intervention after all testing phases. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| MyPlan 2.0 | Behavioral | MyPlan 2.0 consists of five sessions. During these five sessions the following behaviour change techniques are used to motivate users to be more physically active or to sit less: exploring risk perceptions and perceived benefits, exploring social support, providing feedback, action planning, coping planning and monitoring. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in objective total, light and moderate-to-vigorous physical activity (PA) | Change in amount of total, light and moderate-to-vigorous physical activity, measured via accelerometers | Pretest, posttest (6 weeks) and follow-up (6 months) |
| Change in objective sedentary behaviour | Change in amount of total sitting time, measured via accelerometers | Pretest, posttest (6 weeks) and follow-up (6 months) |
| Change in self-reported total, light and moderate-to-vigorous physical activity (PA) | Change in amount of total, light and moderate-to-vigorous physical activity, measured via the International Physical Activity Questionnaire (IPAQ) | Pretest, posttest (6 weeks) and follow-up (6 months) |
| Change in self-reported sedentary behaviour | Change in amount of total sitting time, measured via the LASA sedentary behaviour self-report questionnaire | Pretest, posttest (6 weeks) and follow-up (6 months) |
| Measure | Description | Time Frame |
|---|---|---|
| Change in self-efficacy | Change in amount of self-efficacy to change behaviour, measured via 3 validated items (questionnaire) | Pretest, after week 1, after week 2, after week 3, after week 4, posttest (6 weeks), and follow-up (6 months) |
| Change in outcome expectancies |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Ilse De Bourdeaudhuij, Professor | University Ghent | Principal Investigator |
| Geert Crombez, Professor | University Ghent | Principal Investigator |
| Maïté Verloigne, PostDoc | University Ghent | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Department of Movement and Sports Sciences | Ghent | 9000 | Belgium |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 31376274 | Derived | Poppe L, De Bourdeaudhuij I, Verloigne M, Shadid S, Van Cauwenberg J, Compernolle S, Crombez G. Efficacy of a Self-Regulation-Based Electronic and Mobile Health Intervention Targeting an Active Lifestyle in Adults Having Type 2 Diabetes and in Adults Aged 50 Years or Older: Two Randomized Controlled Trials. J Med Internet Res. 2019 Aug 2;21(8):e13363. doi: 10.2196/13363. |
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| ID | Term |
|---|---|
| D002908 | Chronic Disease |
| D009043 | Motor Activity |
| D003924 | Diabetes Mellitus, Type 2 |
| D000068356 | Self-Control |
| ID | Term |
|---|---|
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D001519 | Behavior |
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Randomized controlled trial with two groups: intervention group and waiting-list control group
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Outcome expectancies regarding the behaviour change, measured via 3 validated items (questionnaire) |
| Pretest, after week 1, after week 2, after week 3, after week 4, posttest (6 weeks), and follow-up (6 months) |
| Change in risk perception | Risk perception about the behaviour, measured via 3 validated items (questionnaire) | Pretest, after week 1, after week 2, after week 3, after week 4, posttest (6 weeks), and follow-up (6 months) |
| Change in intention | Amount of intention to change the behaviour, measured via 3 validated items (questionnaire) | Pretest, after week 1, after week 2, after week 3, after week 4, posttest (6 weeks), and follow-up (6 months) |
| change in action planning | Amount of action planning for behaviour change, measured via 3 validated items (questionnaire) | Pretest, after week 1, after week 2, after week 3, after week 4, posttest (6 weeks), and follow-up (6 months) |
| change in coping planning | Amount of coping planning for behaviour change, measured via 3 validated items (questionnaire) | Pretest, after week 1, after week 2, after week 3, after week 4, posttest (6 weeks), and follow-up (6 months) |
| D003920 | Diabetes Mellitus |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D004700 | Endocrine System Diseases |
| D012919 | Social Behavior |