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Adolescent Fitness Assessment Program (AFAP)

2012年6月25日 更新者:University of Western Ontario, Canada

Increasing Self-efficacy and VO2 Max Scores in Obese Adolescents: a Peer Modeling Intervention

The purpose of this study is to implement a peer modeling intervention to improve self-efficacy and aerobic fitness in obese youth. A total of 40 obese (defined as Body Mass Index greater than the 95th percentile for age and gender) youth will participate in this study.

調査の概要

状態

完了

条件

詳細な説明

There has been a dramatic increase in the prevalence of overweight and obese children in all regions of Canada. In fact, Canada has one of the highest rates of childhood obesity compared to other developed countries. This is disconcerting because this preventative condition is strongly associated with the risk of future disease, such as adult obesity, insulin resistance, type 2 diabetes, cardiovascular problems and psychosocial distress. This trend is a driving factor to develop effective strategies for assessment and intervention.

Aerobic fitness is the ability of the cardiovascular and respiratory system to deliver oxygen to working muscles and utilize that oxygen to produce energy. Aerobic fitness is a strong indicator of physical activity and also correlates with the aforementioned diseases. It is measured as peak ventilatory oxygen (peak VO2; mL/kg min), and is evaluated using a maximal incremental exercise protocol on a treadmill, whereby expired gases are analyzed using a metabolic cart. Aerobic fitness values are inconsistent in youth, particularly obese youth. This discrepancy is due to low self-efficacy. Self-efficacy refers to the belief that one has the power and capabilities to produce an effect. Low self-efficacy is prominent in obese youth because they lack actual and perceived physical competence and social support. This may translate into less effort invested by this population into physical activity, and by the same token, aerobic fitness tests. To date, no experimental studies have attempted to address these psychological variables and apply an intervention to achieve accurate peak VO2 values in obese adolescents.

Peer modelling is the demonstration of particular behaviors that are learned observationally and is a powerful source of self-efficacy. This mode of learning has been very successful in increasing the consumption of new foods (36 subjects) and activity levels (100 subjects) in children. Based on this success, it would suggest that the investigators could confidently apply it to this study. Therefore the main objective is to examine the effect of a modeling intervention (DVD film) on self-efficacy and peak VO2 in obese youth during a maximal treadmill test. Models will demonstrate and articulate increased confidence to perform the test and offer a variety of strategies to cope with the maximal effort and overcome the associated challenges during the test (e.g. shortness of breath, sweating, and increased heart rate). The models will not be participants in the study.

Obese (defined as Body Mass Index greater than the 95th percentile for age and gender) youth (10-17 years, N = 40) who receive written consent from a parent or guardian will be asked to participate in the study. Prior to undertaking the aerobic fitness test, children are required to seek approval from their family physician by completing the Physical Activity Readiness Questionnaire (PAR-Q).

Participants will be randomized after baseline measures are completed into one of two conditions: peer modeling intervention or control to ensure group equivalency. Following randomization, participants in the intervention group will watch the peer modeling DVD film in the lab. Those in the control group will view a DVD film of similar length about nutrition. After seven days, participants in both groups will return for follow-up. One week is a suitable interval because it provides time for participants to reflect on any information they received from the DVD films and minimize external confounding factors, while not providing enough time to see changes in fitness (which requires approximately 3 months). Prior to the second exercise test, participants will watch the DVD film they viewed the previous week. Afterwards, participants will complete their peak VO2 test and self-reported measures. All participants will be asked not to change their normal physical activity patterns during the week.

To complete a peak VO2 test, participants will be required to complete a maximal incremental exercise protocol on a treadmill. The test will be conducted by trained personnel and terminated when participants are unable to continue the protocol, or when their vital signs warranted discontinuation.

The results of this RCT will provide an accurate measurement of aerobic fitness, which is crucial to assessing health status, risk of disease and assisting in planning programs aimed at improving quality of life in adolescents.

研究の種類

介入

入学 (実際)

49

段階

  • 初期フェーズ 1

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

    • Ontario
      • London、Ontario、カナダ、N6A 5B9
        • Exercise and Health Psychology Laboratory

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

10年~17年 (子)

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:

  • Children and adolescents aged 10-17 years who are obese, defined as Body Mass Index greater than the 95th percentile for age and gender

Exclusion Criteria:

  • Participants who smoke, are pregnant or have an illness or disease will be excluded from the study.

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: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:ダブル

武器と介入

参加者グループ / アーム
介入・治療
実験的:Peer modeling
Participants watch a video geared to increase confidence in ability to preform fitness test. Male participants will watch a video of a male adolescent completing the fitness test and talking about coping mechanisms used to preform to the best of his ability. Female participants will watch a video of a female adolescent completing the fitness test and talking about coping mechanisms used to preform to the best of her ability.
Participants watch a video of an adolescent completing the fitness test and explaining coping mechanisms to preform the test well.
他の名前:
  • Observational Learning
  • Coping Model
アクティブコンパレータ:Control
Participants watch a video unrelated to the fitness test and self-efficacy. The video depicts healthy food and nutrition options.
watching a video unrelated to the fitness test and self-efficacy
他の名前:
  • アクティブコントロール
  • 接触制御

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
Physiological measure: Aerobic Fitness
時間枠:Baseline (day 1) and follow-up (day 7)
Changes in aerobic fitness from baseline (day 1) to follow-up (day 7) will be evaluated by a trained exercise physiologist using a standardized, maximal incremental exercise protocol (Modified Bruce protocol) on a treadmill. Expired gases will be analyzed using a metabolic cart (Cosmed Quark B2 cardiopulmonary testing, Image Monitoring). Peak oxygen consumption (Peak VO2) will be determined by taking the highest values during a 15 second period and expressed in absolute (l/min) and relative (ml/kg/min) units with the latter unit used for subsequent analysis.
Baseline (day 1) and follow-up (day 7)
Psychological: Self-Efficacy
時間枠:Baseline (day 1) and follow-up (day 7)
Changes in self-efficacy from baseline (day 1) to follow-up (day 7) will be evaluated by an 18-item Self-Efficacy Scale (adapted from McAuley & Milhalko, 1998) to evaluate participants' confidence to successfully perform increasing intensities and durations of physical activity.
Baseline (day 1) and follow-up (day 7)

二次結果の測定

結果測定
メジャーの説明
時間枠
Changes in variability (standard deviation)
時間枠:Baseline (day 1) and follow-up (day 7)
Changes in variability (standard deviation) in the aerobic fitness and self-efficacy data will be analyzed using statistical software.
Baseline (day 1) and follow-up (day 7)

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。

捜査官

  • 主任研究者:Harry Prapavessis, PhD、The University of Western Ontario

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。

一般刊行物

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

2010年9月1日

一次修了 (実際)

2012年4月1日

研究の完了 (実際)

2012年5月1日

試験登録日

最初に提出

2011年4月21日

QC基準を満たした最初の提出物

2011年6月23日

最初の投稿 (見積もり)

2011年6月27日

学習記録の更新

投稿された最後の更新 (見積もり)

2012年6月26日

QC基準を満たした最後の更新が送信されました

2012年6月25日

最終確認日

2012年6月1日

詳しくは

本研究に関する用語

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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