Physical Activity Clinical Trial
Official title:
Internet-based Physical Activity Intervention
The purpose of this study is to determine whether access to a website with personalized feedback on physical activity level and suggestions to increase physical activity results in improvements in self-reported physical activity, anthropometrics and physiological measurements
Status | Completed |
Enrollment | 12287 |
Est. completion date | May 2009 |
Est. primary completion date | May 2009 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Healthy adults - Physically inactive in leisure time (assessed by self reported questionnaire) Exclusion Criteria: - Presence of serious heart problems or not being able to perform everyday activities - Highly physically active in leisure time (assessed by self reported questionnaire) |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Basic Science
Country | Name | City | State |
---|---|---|---|
Denmark | National Institute of Public Health | Copenhagen | |
Denmark | Municipality of Frederiksberg | Frederiksberg | |
Denmark | Municipality of Silkeborg | Silkeborg | |
Denmark | Municipality of Varde | Varde |
Lead Sponsor | Collaborator |
---|---|
University of Southern Denmark | Rigshospitalet, Denmark |
Denmark,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Self reported physical activity | Physical activity was assessed self reported with the International Physical Activity Questionnaire (IPAQ) | after 3 month | No |
Primary | Self reported physical activity | Physical activity was assessed self reported with the International Physical Activity Questionnaire (IPAQ) | After 6 month | No |
Secondary | Body weight | Body weight was measured to the nearest 0.1 kg and percent point with a Segmeantal Body Composition Analyser (type BC-418 MA, Tanita Corp., Tokyo, Japan). | after 3 month | No |
Secondary | Fat percentage | Fat percentage was measured to the nearest 0.1 kg and percent point with a Segmeantal Body Composition Analyser (type BC-418 MA, Tanita Corp., Tokyo, Japan). | after 3 month | No |
Secondary | Hip and Waist circumference | Hip and waist circumference was measured with a body tape (Chasmors WM02 Body Tape, Chasmors Ltd.,London, United Kingdom) to the nearest 1.0 cm. Waist circumference was measured midway between the iliac crest and the costal margin following a quiet expiration, and lastly hip circumference was measured at the maximal circumference over the buttocks and below the iliac crest. | after 3 month | No |
Secondary | blood pressure | Systolic and diastolic blood pressure were measured by fully automatic clinically validated blood pressure monitors (UA 779, UA-767 Plus 30 or UA 767 PC, A&D Company Ltd, Tokyo, Japan) | 3 month | No |
Secondary | Aerobic fitness | Estimated during a max (watt-max) or a sub-maximal test on a ergometer bike depending on the physical condition of the participant (Ergomedic 828E, Monark Exercise AB, Vansbro, Sweden). One of the following conditions contraindicated participation in the watt-max test: Any heart-related disease, chest pain, hypertension (>160/100 mmHg), heart or lung (pulmonary) medication, pregnancy and muscle, joint or skeletal problems. The sub-max test was contradicted by hypertension (>180/110 mmHg), severe heart-related disease, certain types of heart medication, muscle, joint or skeletal problems. | after 3 month | No |
Secondary | Arm muscle strength | Arm mucle strength was measured by bending of the arms with a Takei TKK 5402 digital back strength dynamometer (Takei Scientific Instruments Co. Ltd., Tokyo, Japan). The test was performed with maximal exertion. | after 3 month | No |
Secondary | blood samples | Non-fasting venous blood samples were collected for future analyses of P-cholesterol, P-triglyceride, and haemoglobin A1c and for biobank storage. | After 3 months | No |
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