HEALTH AND EXERCISE IN THE DEFENSE FORCES

September 11, 2019 updated by: Tampere University Hospital

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

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

Interventional

Enrollment (Anticipated)

500

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Tampere, Finland, 33014
        • Recruiting
        • Kai Parkkola
        • Principal Investigator:
          • EMILIA PIETILÄINEN, MD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

19 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Voluntaries armed forces workers.

Exclusion Criteria:

  • Health enough to participate the military fitness test.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

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

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 16, 2018

Primary Completion (Anticipated)

December 1, 2019

Study Completion (Anticipated)

July 1, 2020

Study Registration Dates

First Submitted

April 25, 2018

First Submitted That Met QC Criteria

May 16, 2018

First Posted (Actual)

May 29, 2018

Study Record Updates

Last Update Posted (Actual)

September 12, 2019

Last Update Submitted That Met QC Criteria

September 11, 2019

Last Verified

September 1, 2019

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)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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.

Clinical Trials on Physical Condition, Minor Psychological Component

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