CClinicalTrials.gg
Status unknownNCT03539679Updated Sep 12, 2019

HEALTH AND EXERCISE IN THE DEFENSE FORCES

An interventional study of Encouraging physical activity. in Physical Condition, Minor Psychological Component, sponsored by Tampere University Hospital. Status unknown at 1 site in Finland. Open to participants aged 19 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-09-12.

Sponsored by Tampere University Hospital · Not applicable, Interventional, and Other

The sponsor has not verified this record recently (last verified Sep 2019), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
500
Allocation
Randomized
Ages
19 Years to 60 Years
Sex
All
01

Study summary

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.

Read the 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.

02

Conditions studied

  • Physical Condition, Minor Psychological Component

Keywords

  • Exercise, sickness absences, health, military fitness
03

In context

Lead sponsor

Tampere University Hospital is the lead sponsor of 209 studies on the registry; 56 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Voluntaries armed forces workers.

Exclusion criteria

Exclusion Criteria:

  • Health enough to participate the military fitness test.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
500 participants (estimated)

Study arms

  • Experimental
    Encouraging physical activity

    Encouraging physical activity by using motion sensor and feedback.

    Other: Encouraging physical activity.

  • No intervention
    CONTROL GROUP

    No intervention.

Interventions

  • OtherEncouraging physical activity.

    Encouraging physical activity with motion sensor's feedback.

06

What researchers measure

Primary outcomes

  1. Better physical condition.

    12-minutes running test are measured.

    Time frame: 6 months.

  2. Less sick leaves.

    The amount of sick leaves are measured.

    Time frame: From past 12 months up to next 12 months.

Secondary outcomes

  1. Positive changes in the TELI v 1.0 questionnaire.

    Number of participants with better outcome in health habits (sleeping, eating, exercise).

    Time frame: 6 months.

  2. Better physical condition.

    Muscular fitness test.

    Time frame: 6 months.

Other outcomes

  1. Better physical condition.

    12-minutes running test are measured.

    Time frame: 12 months.

  2. Better physical condition.

    Muscular fitness test.

    Time frame: 12 months.

  3. Positive changes in the TELI v 1.0 questionnaire.

    Number of participants with better outcome in health habits (sleeping, eating, exercise).

    Time frame: 12 months.

07

Study locations

1 of 1 sites recruiting
  • Kai Parkkola
    Tampere, 33014, Finland
    • EMILIA PIETILÄINEN, MD · Principal investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 12, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03539679
Lead sponsor
Tampere University Hospital
Collaborators
Tampere University, University of Jyvaskyla, UKK Institute
Responsible party
Sponsor
First posted
May 29, 2018
Start date
May 16, 2018
Primary completion
Dec 2019 (estimated)
Completion
Jul 2020 (estimated)
Last update
Sep 12, 2019

Study contacts

KAI I PARKKOLA, PROF EMER
Contact
kai.parkkola@staff.uta.fi
+358 40 5003116
HEIKKI KYRÖLÄINEN, PROF
Contact
heikki.kyrolainen@jyu.fi
+358 40 5408703
KAI I PARKKOLA, PROF EMER
study director · PROF EMER, UNIVERSITY OF TAMPERE
HEIKKI KYRÖLÄINEN, PROF
study director · PROF, UNIVERSITY OF JYVÄSKYLÄ

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Sep 2019. You cannot join it, but the record below documents what was studied.

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