- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03539679
HEALTH AND EXERCISE IN THE DEFENSE FORCES
TERVEYS JA LIIKUNTA PUOLUSTUSVOIMISSA
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.
Study Overview
Status
Intervention / Treatment
Detailed Description
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
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: KAI I PARKKOLA, PROF EMER
- Phone Number: +358 40 5003116
- Email: kai.parkkola@staff.uta.fi
Study Contact Backup
- Name: HEIKKI KYRÖLÄINEN, PROF
- Phone Number: +358 40 5408703
- Email: heikki.kyrolainen@jyu.fi
Study Locations
-
-
-
Tampere, Finland, 33014
- Recruiting
- Kai Parkkola
-
Principal Investigator:
- EMILIA PIETILÄINEN, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Voluntaries armed forces workers.
Exclusion Criteria:
- Health enough to participate the military fitness test.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Encouraging physical activity
Encouraging physical activity by using motion sensor and feedback.
|
Encouraging physical activity with motion sensor's feedback.
|
No Intervention: CONTROL GROUP
No intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Better physical condition.
Time Frame: 6 months.
|
12-minutes running test are measured.
|
6 months.
|
Less sick leaves.
Time Frame: From past 12 months up to next 12 months.
|
The amount of sick leaves are measured.
|
From past 12 months up to next 12 months.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
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).
|
6 months.
|
Better physical condition.
Time Frame: 6 months.
|
Muscular fitness test.
|
6 months.
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Better physical condition.
Time Frame: 12 months.
|
12-minutes running test are measured.
|
12 months.
|
Better physical condition.
Time Frame: 12 months.
|
Muscular fitness test.
|
12 months.
|
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).
|
12 months.
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: KAI I PARKKOLA, PROF EMER, PROF EMER, UNIVERSITY OF TAMPERE
- Study Director: HEIKKI KYRÖLÄINEN, PROF, PROF, UNIVERSITY OF JYVÄSKYLÄ
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- R16189
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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