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Comparison of Affect-based, Self-selected, and Traditional Exercise Prescriptions

2018年7月6日 更新者:Zachary、Duke University
This study will evaluate adherence to four types of walking programs. Participants will be randomized to walking programs that included either (1) affect-based exercise intensity, (2) self-selected (or "choice-based") exercise intensity, (3) heart-rate based exercise intensity, or (4) heart-rate guided exercise intensity with the emphasis on affective benefits.

調査の概要

詳細な説明

The purpose of this study is to determine if an "affect-based" or "choice-based" exercise prescription is more effective for behavior change than a traditional, "moderate-intensity" exercise prescription. Prior research suggests that "choice-based" or "self-selected" exercise intensity is more pleasant and adhered to than "moderate-intensity exercise" (Williams et al., 2014). Similarly, affect-based exercise prescriptions (i.e., an exercise prescription where intensity is regulated based on the pleasure-displeasure one feels while exercising) appear to have merit (Baldwin, Kangas, Denman, Smits, Yamada, & Otto, 2016).

However, choice-based and affect-based exercise prescriptions have not been compared to each other. Further, it is unknown if it is the intensity regulation that matters (e.g., "choose an intensity that feels good" or the focus on affect (e.g., "focus on feeling good). Third, prior research has not objectively measured physical activity behavior.

研究の種類

介入

入学 (実際)

159

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

    • North Carolina
      • Durham、North Carolina、アメリカ、27701
        • Duke University IBRC Lab

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:

  • Must be fluent in English
  • Must be able to walk
  • Exercise less than 90 minutes per week at a moderate-intensity
  • Must be able to attend laboratory visits
  • Must have mobile internet accent and a personal smartphone (iPhone iOS 9+ or Android OS 4.3+)
  • Can safely exercise at an intensity that is at least "moderate"

Exclusion Criteria:

  • People who are recommended to have medical clearance prior to exercising, according to the American College of Sports Medicine's preparticipation screening criteria, will be excluded

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

  • 主な目的:防止
  • 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
実験的:Choice-No Affect
These participants self-select (i.e., choose) their exercise intensity with the goal of walking 30-60 minutes on most days of the week. For safety reasons, they are instructed not to exceed 59% of their heart rate reserve. This is choice-based exercise intensity with no focus on positive affect.
Participants are instructed to choose whichever intensity they want, rather than regulate their intensity based on heart rate.
実験的:Choice-Affect
These participants self-select their exercise intensity with the goal of walking 30-60 minutes on most days of the week. They're instructed to choose the intensity that makes them feel the best. For safety reasons, they are instructed not to exceed 59% of their heart rate reserve. This is choice-based exercise intensity with a focus on positive affect.
Participants are instructed to choose whichever intensity they want, rather than regulate their intensity based on heart rate.
Participants are instructed to focus on feeling good while exercising.
実験的:No Choice-Affect
These participants regulate their exercise intensity using their heart rate, with the goal of walking 30-60 minutes on most days of the week. The intensity is "moderate" according to the American College of Sports Medicine (40-59% of their heart rate reserve). Meanwhile, these participants are instructed to focus on the "good feelings" that come with exercise. this is heart rate-based exercise intensity with a focus on positive affect.
Participants are instructed to focus on feeling good while exercising.
Participants are instructed to regulate their exercise intensity based on their heart rate.
アクティブコンパレータ:No Choice-No Affect
These participants regulate their exercise intensity using their heart rate, with the goal of walking 30-60 minutes on most days of the week. The intensity is "moderate" according to the American College of Sports Medicine (40-59% of their heart rate reserve). This is heart rate-based exercise intensity with no focus on positive affect.
Participants are instructed to regulate their exercise intensity based on their heart rate.

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
Change in objectively measured exercise behavior
時間枠:This will be measured throughout the baseline assessment period (2 weeks) and intervention period (4 weeks)
Minutes per week of objectively measured exercise behavior.
This will be measured throughout the baseline assessment period (2 weeks) and intervention period (4 weeks)

二次結果の測定

結果測定
メジャーの説明
時間枠
Change in self-reported exercise behavior
時間枠:This will be measured throughout the baseline assessment period (2 weeks) and intervention period (4 weeks)
Minutes per week of self-reported exercise behavior that is reported using exercise log.
This will be measured throughout the baseline assessment period (2 weeks) and intervention period (4 weeks)
Change in affective attitudes
時間枠:Measured during baseline assessment period and at the end of the intervention
Affective attitudes toward exercise
Measured during baseline assessment period and at the end of the intervention
Self-reported intrinsic motivation (questionnaires)
時間枠:Two weeks into study intervention
Intrinsic motivation for exercise program
Two weeks into study intervention
Enjoyment
時間枠:Measured at the end of the intervention period (4 weeks)
Enjoyment of exercise program.
Measured at the end of the intervention period (4 weeks)
Change in weight
時間枠:Measured at the beginning and end of the study (6 weeks).
Body weight
Measured at the beginning and end of the study (6 weeks).
Change in resting heart rate
時間枠:Measured at the beginning and end of the study (6 weeks).
Resting heart rate
Measured at the beginning and end of the study (6 weeks).

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

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

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 (実際)

2017年2月21日

一次修了 (実際)

2018年3月29日

研究の完了 (実際)

2018年3月29日

試験登録日

最初に提出

2017年2月2日

QC基準を満たした最初の提出物

2017年2月6日

最初の投稿 (見積もり)

2017年2月9日

学習記録の更新

投稿された最後の更新 (実際)

2018年7月9日

QC基準を満たした最後の更新が送信されました

2018年7月6日

最終確認日

2018年7月1日

詳しくは

本研究に関する用語

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?

はい

IPD プランの説明

The investigators retain ownership of all study data, but are willing to share anonymized data for transparency purposes at the conclusion of the study. Data may be requested by contacting the Principal Investigator.

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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