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Creating Exercise Habits Through Incentives for Routines (Routines)

2016年8月18日 更新者:University of Pennsylvania
The purpose of this study is to determine whether healthy habits can be formed more effectively when people are rewarded for repeated engagement in a given healthy behavior at a specific, routinized time each day rather than at any time.

調査の概要

詳細な説明

The investigators seek to examine the effect of incentives for routine exercise on the development of persistent exercise habits. Specifically, the purpose of this study is to determine whether healthy habits can be formed more effectively when people are rewarded for repeated engagement in a given healthy behavior at a specific, routinized time each day rather than at any time. Through a partnership with a Fortune-500 company, the investigators plan to run a large-scale, randomized field controlled trial with approximately 3,000-4,000 participants aimed at increasing exercise rates (as measured by gym visits). During an incentivized four week intervention period, the investigators will encourage participants to select a two-hour window during the day when they feel they are most willing and able to exercise. Depending on condition, participants will [a] receive no further instruction or incentives (control condition), [b] receive a $3 or $7 bonus for each day they exercise during the incentive period (flexible incentive condition), or [c] receive a $3 or $7 bonus for each day they exercise if and only if they exercise within their specified "workout window" (routine incentive condition). Additionally, participants in a fourth condition, the social routine incentive condition, will face the same incentives as those in the routine incentive condition, but will be required to coordinate the workout window they select with a partner in their office. The investigators predict that the less flexible incentives will lead to greater habit formation than flexible incentives, producing larger and longer-lasting increases in exercise post-intervention. The investigators further predict that coordinating with a workout partner will produce even stronger habit formation. The investigators will collect and analyze data from participants' worksite gyms, which track gym entries and exits, as well as pedometer data when available.

Our experiment will recruit employees at a Fortune-500 company who wish to exercise more. Recruitment will be done through an email and poster campaign. The registration stage will take approximately four weeks. All employees at all offices with on-site gyms will be eligible to enroll and upon enrollment will be asked to select a partner who works in the same office and who is also enrolling. Enrolling employees will also be asked to indicate their preferred daily workout time (a two hour "workout window") and to provide basic demographic and exercise-related information (e.g., gender, age, height, weight, number of gym visits per week). If registration exceeds the target sample size (4,000 employees), priority for enrollment will be given to employees who do not already exercise regularly (at least twice a week). The remaining participants will be assigned to a "holdout control" condition. Once registration is closed, participants will be assigned randomly (at the pairs level) to one of the four experimental conditions.

研究の種類

介入

入学 (実際)

2702

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Pennsylvania
      • Philadelphia、Pennsylvania、アメリカ、19104
        • University of Pennsylvania

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

はい

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Participants must be full-time employees of partner company

Exclusion Criteria:

  • N/A

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 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:Control
Participants in the control group will not receive any additional treatment, apart from receiving daily emails 15 minutes before the start of their self-reported workout window. This is to control for reminder effects that may be present in the other treatment conditions. Participants in this condition will also receive a lump payment upon completion of an exit survey at the end of the intervention to equalize overall compensation.
Participants will receive emails at prespecified times reminding them to exercise, either during a specific two hour window or at any time during the day.
Participants will receive $20 payments for completing post treatment survey.
実験的:Flexible Incentive
Participants in the flexible incentive condition will be paid $3 or $7 for each workout they complete during the treatment period (with a limit of one incentivized workout per day, and twelve incentivized workouts during the four-week treatment period). These participants will receive daily emails 15 minutes before the start of their self-reported workout window, but they can work out anytime of the day and still receive their incentive payment.
Participants will receive emails at prespecified times reminding them to exercise, either during a specific two hour window or at any time during the day.
Participants will be paid $3 or $7 for each workout completed during the appropriate times.
実験的:Routine Incentive
Participants assigned to the routine incentive condition will receive the same treatment as those in the flexible incentive condition except that, in order to receive their incentive payment, they must begin their workout within their two-hour workout window. For instance, if an employee chooses a 2pm to 4pm workout window, she will receive a reminder to exercise at 1:45 pm and must swipe into the gym between 2pm and 4pm in order to receive the $3 or $7 incentive payment.
Participants will receive emails at prespecified times reminding them to exercise, either during a specific two hour window or at any time during the day.
Participants will be paid $3 or $7 for each workout completed during the appropriate times.
実験的:Social Routine Incentive
Participants assigned to this condition will have an identical experience to those in the routine incentive except that both partners who sign up for the study will be required to coordinate and select a common workout window. Thus, both partners will receive their daily reminders at the same time (and will be incentivized for working out at the same time). The incentive payment, however, will not be linked to whether or not a participant's partner completes a workout - only to the participant's own exercise decision.
Participants will receive emails at prespecified times reminding them to exercise, either during a specific two hour window or at any time during the day.
Participants will be paid $3 or $7 for each workout completed during the appropriate times.
Participants will be required to have same "workout window" as partners.
介入なし:Holdout Control
If experimental enrollment exceeds target, exercise data will be collected for these additional participants, but they will receive no intervention of any kind.

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
Average weekly number of 30+ minute visits to company gym
時間枠:Up to one year
Number of times per week participants enter the company gym and exit at least 30 minutes later
Up to one year
Duration of habit
時間枠:Up to one year
Length of time that weekly gym visits takes to return to baseline level
Up to one year

二次結果の測定

結果測定
メジャーの説明
時間枠
Activity level as measured by Fitbit pedometers
時間枠:Up to one year
Number of steps taken during workouts, as measured by Fitbit pedometers
Up to one year

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Katherine L Milkman, PhD、University of Pennsylvania

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始

2015年1月1日

一次修了 (実際)

2016年2月1日

研究の完了 (実際)

2016年2月1日

試験登録日

最初に提出

2015年1月5日

QC基準を満たした最初の提出物

2015年1月20日

最初の投稿 (見積もり)

2015年1月27日

学習記録の更新

投稿された最後の更新 (見積もり)

2016年8月22日

QC基準を満たした最後の更新が送信されました

2016年8月18日

最終確認日

2016年8月1日

詳しくは

本研究に関する用語

追加の関連 MeSH 用語

その他の研究ID番号

  • 821291

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。

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