Columbia Moves Physical Activity
Evaluating Columbia Moves: A Social Network Approach Using a Team Competition and Technology to Increase Physical Activity
調査の概要
詳細な説明
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
-
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South Carolina
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Columbia、South Carolina、アメリカ、29208
- University of South Carolina
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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:
- Insufficiently active as determined by a one-week, accelerometer-based physical activity measurement
- Body mass index (BMI) between 25 kg/m2 and 55 kg/m2
- Between ages 18 and 65 years
- Access to computer with Internet connection
- Smartphone ownership (Android or iOS)
- Willing to be randomized to either one of the two study groups
- Part of a self-selected team of 3-8 eligible individuals
- Members of the same household cannot be part of separate groups
- Able to walk at least 1/4 mile without stopping
Exclusion Criteria:
- Currently lactating, pregnant, or planning to become pregnant during the length of the study
- Diagnosed with type 1 or type 2 diabetes
- Medical or physical contraindications or limitations for engaging in physical activity
- History of major medical or psychiatric conditions
- Currently participating in a physical activity program
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:処理
- 割り当て: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 |
---|---|
アクティブコンパレータ:TECH (Technology)
Participants will receive a theory-based physical activity program.
They will enroll in the study as part of a self-selected group of 3-8 individuals.
They will be provided with a personal step goal and Fitbit Alta HR for self-monitoring physical activity.
They will also have access to a study website that will be accessible across conventional and mobile platforms.
They will be asked to visit the website each week to receive behavior change information and guidance.
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Participants will receive a theory-based physical activity program. They will enroll in the study as part of a self-selected group of 3-8 individuals. They will be provided with a personal step goal and Fitbit Alta HR for self-monitoring physical activity. They will also have access to a study website that will be accessible across conventional and mobile platforms. They will be asked to visit the website each week to receive behavior change information and guidance. Device: Fitbit Alta HR |
実験的:TECH+COMP (Technology + Competition)
Participants will receive the same intervention components as the TECH goup, as well as a study designed team competition.
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Participants will receive the same intervention components as the TECH group, as well as a team competition. The competition will be based on the following two aspects: total daily steps accumulated relative to group size and total number of points retained for achieving weekly physical activity challenges. Device: Fitbit Alta HR |
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 |
---|---|---|
Accelerometer-measured change from Baseline Daily Steps at 3 months and 12 months
時間枠:0, 3, and 12 months
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Change in daily steps
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0, 3, and 12 months
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
---|---|---|
Accelerometer-measured change from Baseline Minutes of Moderate-to-Vigorous Physical Activity at 3 months and 12 months
時間枠:0, 3, and 12 months
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Change in moderate-to-vigorous physical activity
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0, 3, and 12 months
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Change from Baseline in Perceived Social Support for Exercise (Sallis Social Support and Exercise Survey) at 3 and 12 months
時間枠:0, 3, and 12 months
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Change in perceived social support for exercise (scale total score range: 1 to 5, with 1 representing low perceived social support for exercise and 5 representing high perceived social support for exercise; responses to all items are averaged to yield a total final score)
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0, 3, and 12 months
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その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
---|---|---|
Participant Satisfaction (Satisfaction Questionnaire)
時間枠:4 months
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Participant satisfaction with treatment
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4 months
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協力者と研究者
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
- 2018
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?
IPD プランの説明
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。
TECH (Technology)の臨床試験
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Johns Hopkins UniversityNational Institute of Nursing Research (NINR)積極的、募集していない
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The University of QueenslandQueensland University of Technology; Medical Research Future Fund; Metro South Hospital and Health... と他の協力者募集
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University of Wisconsin, MadisonVirginia Commonwealth University募集
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University of Campania "Luigi Vanvitelli"Dentsply Sirona Implants and Consumablesわからない
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Rigshospitalet, DenmarkZimmer Biomet積極的、募集していない
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ConvaTec Inc.わからない