Obesity Clinical Trial
— MOBIGAMEOfficial title:
Mobile Exergaming for Health - Effects of a Serious Game Application for Smartphones on Physical Activity and Exercise Adherence in Type 2 Diabetes Mellitus (Randomized Controlled Trial)
| Verified date | April 2018 |
| Source | University of Basel |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The purpose of this study is to investigate if MOBIGAME (an innovative, mobile phone-based game application) is suitable to increase daily physical activity and physical activity adherence as well as health parameters such as cardiorespiratory fitness, leg strength, glucose metabolism, vascular health and self-determination as well as health related quality of life in the course of a 24-week intervention in comparison to the control group receiving one-time lifestyle counseling.
| Status | Completed |
| Enrollment | 36 |
| Est. completion date | April 2018 |
| Est. primary completion date | April 2018 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 45 Years to 70 Years |
| Eligibility |
Inclusion Criteria: - Informed Consent as documented by signature - Non-insulin-dependent diabetes mellitus (doctor diagnosed) - Body Mass Index >25 kg/m2 - Regular smartphone use during the last year before the study - Motivation to participate in the study for its entire duration of 24 weeks Exclusion Criteria: - Other clinically significant concomitant disease states (e.g., renal failure, hepatic dysfunction, cardiovascular disease, etc.), - Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participant - Previous enrolment into the current study - Participation in other studies in the last four weeks - Systolic blood pressure > 170mmHg, diastolic blood pressure > 100 mmHg - Regular physical activity before the study (=150 min moderate intensity daily PA per week or >1 endurance or strength training session per week of more than 30 min in duration) |
| Country | Name | City | State |
|---|---|---|---|
| Switzerland | Division of Sports and Exercise Medicine, Department of Sport, Exercise and Health, University of Basel | Basel | BS |
| Lead Sponsor | Collaborator |
|---|---|
| University of Basel | Swiss National Science Foundation |
Switzerland,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Other | Change from baseline self-determination at 24 weeks | Self-determination (intrinsic motivation, perceived competence, perceived choice, perceived usefulness measured via the score in an abridged, 12-item version of the Intrinsic Motivation Inventory. | Baseline and 24 weeks | |
| Other | Change from baseline cardiorespiratory fitness at 24 weeks | Aerobic capacity measured as VO2peak. | Baseline and 24 weeks | |
| Other | Change from baseline six minute walking distance at 24 weeks | Measured via the Six Minute Walk Test | Baseline and 24 weeks | |
| Other | Change from baseline isometric leg strength at 24 weeks | Measured as maximal isometric force and rate of force development. | Baseline and 24 weeks | |
| Other | Change from baseline leg strength endurance at 24 weeks | Assessed as maximum number of repetitions in the Sit-to-Stand Test (STS) | Baseline and 24 weeks | |
| Other | Change from baseline glucose metabolism at 24 weeks | Fasting glucose, glycated hemoglobin (HbA1c), fasting C-peptides, fasting insulin levels and insulin resistance, measured as homeostasis model assessment (HOMA) index. | Baseline and 24 weeks | |
| Other | Change from baseline inflammatory markers at 24 weeks | Total cholesterol, LDL- and HDL-cholesterol, triglycerides, apolipoprotein B, irisin, adiponectin and interleukin-6 | Baseline and 24 weeks | |
| Other | Change from baseline central blood pressure at 24 weeks | Baseline and 24 weeks | ||
| Other | Change from baseline pulse wave reflection at 24 weeks | Measured as augmentation index. | Baseline and 24 weeks | |
| Other | Change from baseline arterial stiffness at 24 weeks | Measured as aortic pulse wave velocity. | Baseline and 24 weeks | |
| Other | Change from baseline microvascular function at 24 weeks | Measured as retinal vessel diameters. | Baseline and 24 weeks | |
| Other | Change from baseline health-related quality of life (HRQOL) at 24 weeks | Assessed with score in the 36-item Short Form questionnaire (SF-36). | Baseline and 24 weeks | |
| Other | Change from baseline fatigue at 24 weeks | Measured via the score in the 13-item FACIT Fatigue Scale. | Baseline and 24 weeks | |
| Other | Perceived acceptance of intervention | Measured via the Technology Acceptance Model (TAM) questionnaire. | 24 weeks | |
| Primary | Change from baseline daily physical activity at 24 weeks | Measured as steps per day. | Baseline and 24 weeks | |
| Secondary | Adherence to the intervention | Measured as usage log entries (intervention group) and self-reported exercise log entries (control group). | 24 weeks |
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