確率に逆らえ：長時間座り仕事のための運動予測とモチベーション戦略
オッズに逆らえ：長時間座り仕事のための運動予測とモチベーション戦略
This study aims to see if a new approach called "Exercise Forecasting" can help people with jobs with a lot of sitting get more active. It also tests if using this method in personal motivational messages makes it easier for them to exercise.
The main questions it aims to answer are:
- Can "Exercise Forecasting" be used effectively for people in jobs requiring long periods of sitting?
- Do these tailored, proactive messages encourage people to exercise more and sit less?
Participants will:
- Wear the provided smartwatch and answer two questions per day
- Receive customized motivational messages
調査の概要
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
-
-
Wisconsin
-
Madison、Wisconsin、アメリカ、53705
- University of Wisconsin - Madison
-
-
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:
- Can communicate in English
- Currently participate in less than 30 minutes of regular physical activity per week.
- Healthy male/female, age >=40
- Currently working in a prolonged sitting job (e.g., truck driver or office worker).
- Have been working in this industry/business for at least one year.
Exclusion Criteria:
- Have had a heart attack within the past three months
- Surgery in the past three months
- Recent stroke, mini-stroke/TIA in the past three months
- Recent seizure disorder or epilepsy in the past three months
- Had an aortic aneurysm before
- Have a medical condition or physical limitation that makes physical activity unsafe
- Currently meeting or exceeding physical activity guidelines (≥150 minutes/week of moderate-intensity activity or equivalent).
- Cannot wear a smartwatch for 30 days.
- Do not want to install a study APP in smart phone for 30 days.
- Cannot respond to the study APP notification for 30 days.
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：防止
- 割り当て：非ランダム化
- 介入モデル：並列代入
- マスキング：なし（オープンラベル）
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的：Office workers
Participants who are office workers |
Participants receive motivational messages customized to their previously stated expectations and goals. |
|
実験的：Truck drivers
Participants who are truck drivers |
Participants receive motivational messages customized to their previously stated expectations and goals. |
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 |
|---|---|---|
|
Correlation between biometric data and self-reported exercise
時間枠：20 days
|
Biometric data will be collected through the smartwatch. Participants are also asked to self-report what type of exercise they did. These will be correlated to learn whether probability of daily activity can be predicted. |
20 days
|
|
Acceptability of customized messages
時間枠：30 days
|
Acceptability will be qualitatively evaluated using one-on-one interviews, with semi-structured interview guides. Acceptability will be analyzed using thematic analyses. |
30 days
|
|
Feasibility - retention rate
時間枠：30 days
|
Retention rate will be measured by the number of participants who complete the study. |
30 days
|
|
Change in level of physical activity when receiving custom motivational messages
時間枠：Baseline to 30 days
|
Using data collected from the smartwatch, level of physical activity will be compared between pre-motivational messaging and post-motivational messaging. |
Baseline to 30 days
|
|
Change in System Usability Scale (SUS) Score
時間枠：Baseline to 30 days
|
SUS is a 10-item questionnaire about system usability. It is scored on a 5-point Likert scale, where 1 = strongly disagree and 5 = strongly agree. Scores range from 0-100 (due to reverse scoring and 2.5 multiplication). Higher scores indicate greater usability. |
Baseline to 30 days
|
協力者と研究者
捜査官
- 主任研究者：Wan-chin Kuo, PhD, RN、University of Wisconsin, Madison
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
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
- 2026-0224
- UWMSN | Nursing | Administrati (その他の識別子：UW Madison)
- T42OH008434 (米国 NIH グラント/契約)
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
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。