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.
調査の概要
詳細な説明
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.
研究の種類
入学 (予想される)
段階
- 適用できない
連絡先と場所
研究場所
-
-
-
Tampere、フィンランド、33014
- 募集
- Kai Parkkola
-
主任研究者:
- EMILIA PIETILÄINEN, MD
-
-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Voluntaries armed forces workers.
Exclusion Criteria:
- Health enough to participate the military fitness test.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:他の
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Encouraging physical activity
Encouraging physical activity by using motion sensor and feedback.
|
Encouraging physical activity with motion sensor's feedback.
|
|
介入なし:CONTROL GROUP
No intervention.
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Better physical condition.
時間枠:6 months.
|
12-minutes running test are measured.
|
6 months.
|
|
Less sick leaves.
時間枠: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.
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Positive changes in the TELI v 1.0 questionnaire.
時間枠:6 months.
|
Number of participants with better outcome in health habits (sleeping, eating, exercise).
|
6 months.
|
|
Better physical condition.
時間枠:6 months.
|
Muscular fitness test.
|
6 months.
|
その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Better physical condition.
時間枠:12 months.
|
12-minutes running test are measured.
|
12 months.
|
|
Better physical condition.
時間枠:12 months.
|
Muscular fitness test.
|
12 months.
|
|
Positive changes in the TELI v 1.0 questionnaire.
時間枠:12 months.
|
Number of participants with better outcome in health habits (sleeping, eating, exercise).
|
12 months.
|
協力者と研究者
捜査官
- スタディディレクター:KAI I PARKKOLA, PROF EMER、PROF EMER, UNIVERSITY OF TAMPERE
- スタディディレクター:HEIKKI KYRÖLÄINEN, PROF、PROF, UNIVERSITY OF JYVÄSKYLÄ
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (予想される)
研究の完了 (予想される)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- R16189
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
米国で製造され、米国から輸出された製品。
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。