HEALTH AND EXERCISE IN THE DEFENSE FORCES
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|ClinicalTrials.gov Identifier: NCT03539679|
Recruitment Status : Recruiting
First Posted : May 28, 2018
Last Update Posted : September 12, 2019
The most important goal is to create a cost-effective, stimulating model for improving the employee's quality of life, work ability, and job satisfaction in the military operating environment. This is achieved by finding out how to activate an individual with the phone-based gaming and web-based feedback system to improve his physical condition. This study also tries to find out the adequate amount of physical activity to maintain the physical health of workers.
Personnel work ability, to work safe in service and effective operation capability of emergency forces require a worker's state of total well-being, in which the health and the physical condition are important parts. The changes in these affects the individual's fitness to military. This study develops a model to encourage an individual to carry out physical activity by himself. This will lead to reduce the sick leaves and improve the health and fitness.
Physical activity reduces morbidity. Professional soldiers must maintain their physical condition and skills. The study explores the optimum amount of working-age physical activity. It helps to maintain the working ability and one's fitness to field operations. With the help of the developed model it is possible cost-effectively activate a large number of employees to move more and to live more healthily.
|Condition or disease||Intervention/treatment||Phase|
|Physical Condition, Minor Psychological Component||Other: Encouraging physical activity.||Not Applicable|
In this study it will be used motion sensors which are sending feedback to individuals mobile phone. Feedback is also given by email and in an interview after analyzing data from cloud service.
In the beginning of the study it will analyzed blood test, salivary test, body composition, height weight and basic motion. All volunteers are also answering a questionnaire.
There will be an intervention group and a control group. The intervention group will receive feedback during the all six months they are carrying the motion sensor.
After 6 and 12 months the basic analyzes will be repeated. Sick leaves and the changes in the muscular fitness test and changes in the 12-minutes running test will be analyzed.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||500 participants|
|Intervention Model:||Parallel Assignment|
|Intervention Model Description:||Intervention group and control group.|
|Masking Description:||Exclusion criteria is that a volunteer must be health enough to have permission to take part in the military fitness tests.|
|Official Title:||TERVEYS JA LIIKUNTA PUOLUSTUSVOIMISSA|
|Actual Study Start Date :||May 16, 2018|
|Estimated Primary Completion Date :||December 2019|
|Estimated Study Completion Date :||July 2020|
Experimental: Encouraging physical activity
Encouraging physical activity by using motion sensor and feedback.
Other: Encouraging physical activity.
Encouraging physical activity with motion sensor's feedback.
No Intervention: CONTROL GROUP
- Better physical condition. [ Time Frame: 6 months. ]12-minutes running test are measured.
- Less sick leaves. [ Time Frame: From past 12 months up to next 12 months. ]The amount of sick leaves are measured.
- Positive changes in the TELI v 1.0 questionnaire. [ Time Frame: 6 months. ]Number of participants with better outcome in health habits (sleeping, eating, exercise).
- Better physical condition. [ Time Frame: 6 months. ]Muscular fitness test.
- Better physical condition. [ Time Frame: 12 months. ]12-minutes running test are measured.
- Better physical condition. [ Time Frame: 12 months. ]Muscular fitness test.
- Positive changes in the TELI v 1.0 questionnaire. [ Time Frame: 12 months. ]Number of participants with better outcome in health habits (sleeping, eating, exercise).
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03539679
|Contact: KAI I PARKKOLA, PROF EMER||+358 40 firstname.lastname@example.org|
|Contact: HEIKKI KYRÖLÄINEN, PROF||+358 40 email@example.com|
|Tampere, Finland, 33014|
|Principal Investigator: EMILIA PIETILÄINEN, MD|
|Study Director:||KAI I PARKKOLA, PROF EMER||PROF EMER, UNIVERSITY OF TAMPERE|
|Study Director:||HEIKKI KYRÖLÄINEN, PROF||PROF, UNIVERSITY OF JYVÄSKYLÄ|