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The Effects of Exercise on Physiological and Psychological Parameters in an Asthmatic Population

2011年12月31日 更新者:Kasee Hildenbrand、Washington State University
Exercise has been shown to have extensive health benefits both in normally functioning adults as well as in adults with asthma. A program of regular aquatic exercise may have unique benefits in the asthmatic population because of the known aerobic capacity development typical of such programs, combined with the unique value of immersion-produced improvements in respiratory endurance and cardiac output. The purpose of this study is to explore the effects of a 12 week long aquatic endurance training program on several physiological and psychological parameters related to coronary heart disease and type II diabetes in an asthmatic population.

調査の概要

状態

完了

介入・治療

詳細な説明

The study will run from August 2008 to May 2009. Recruitment and screening of participants will occur from August to December 2008 for inclusion into the clinical trial. Prior to the clinical trial participants will have a one hour informational session to clearly present the study, obtain signed informed consent and set up fitness/blood appointments for data collection. Data collection will begin the first week of school in January. The 12-week exercise protocol will start the second week of school and continue through the middle of April. Research participants will not have any exercise session during spring break (March 16-20). Final data collection will occur during the last two weeks of school. Pre-treatment and post-treatment data collection will include a fitness assessment and blood draw. Medication usage for asthma will be monitored on a weekly basis thoughout the clinical trial. Physical activity will also be monitored monthly.

The screening session is a 30-minute session where research participants complete health/behavior questionnaires and a physiological measure of lung function. Information to be collected in the health/behavior questionnaires includes: demographic and behavioral/lifestyle variables (sex, race, age, smoking status, and medical history).

The fitness assessment will be 60 minutes in length. At the beginning of the session participants will complete a survey to assess state anxiety (State-Trait Anxiety Inventory - Trait version Form X-1; Spielberger, Gorsuch, & Lushene, 1970). Heart rate variability will be measured through the ventral placement of 3 electrodes placed on the subject's torso. The areas will be prepped by swabbing with alcohol and lightly scrubbing to remove dead skin. The electrodes will be held in place with a sticky disc and a strip of athletic tape. Heart rate and resting blood pressure will also be taken. Body composition will be assessed using the BodPod system. Research participants will sit in an enclosed capsule (bod pod) for three tests lasting approximately 40 seconds each. Lung function will be assessed using a spirometer to measure the maximal volume of air exhaled over a period of time after a maximal inhalation. To assess cardiorespiratory fitness research participants will complete a VO2 Max test. Participants will ride a bicycle ergometer for approximately 15-20 minutes moving through stages (including a 3 minute warm-up) with progressively higher resistance levels until maximum tolerance. After termination there is a cool-down/recovery period of approximately 3-4 minutes.

The blood draw session will take approximately 30 minutes and participants will be asked to fast (no food or drink) for 12 hours prior to blood draw. Upon check-in participants will complete a series of questionnaires assessing psychological variables stress (Perceived Stress Scale-14 item version Form X-1; Cohen, Kamarck & Mermelstein, 1983), depression (Center for Epidemiological Studies - Depression Scale; Radloff, 1977), and quality of life (Asthma Impact Survey; QualityMetric Health Outcomes Solutions, Lincoln, RI). The quality and quantity of sleep will also be assessed using the Pittsburgh Sleep Quality Index (Buysse, Reynolds, Monk, Berman, & Kupfer, 1989). Once questionnnaires are completed, participants will have their blood drawn by a certified phlebotomist. Three days after the blood draw particpants will be contacted by phone and questioned about current health status.

After the first week of pretreatment data collection, before the training sessions begin, research participants will undergo an explanation and training session to learn how to evaluate their own rate of perceived exertion (RPE). The water-based exercise programs are 3 times a week for 12 weeks. The exercise sessions will begin with a 10-minute warm up and end with a 5-minute cool down period. The conditioning portion of the exercise program will be shorter in duration with lower intensities at the beginning of the 12 weeks. There will be a progression to higher intensities for longer periods of time throughout the 12 weeks using recommendations from the American College of Sports Medicine. Exercise sessions will not exceed 50 minutes.

研究の種類

介入

入学 (実際)

16

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

    • Washington
      • Pullman、Washington、アメリカ、99164
        • Washington State University

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~40年 (大人)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Medically diagnosed and medication managed asthmatics between the ages of 18-40

Exclusion Criteria:

  • outside the age range of 18-40 years old, fear of water, diseases or conditions listed during screening process, or current smoker.

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:非ランダム化
  • 介入モデル:単一グループの割り当て
  • 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:1
Aquatic based exercise
Exercise 3 times each week for a total of 12 weeks. Each session is 50 min. in length.

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
時間枠
Pulmonary Function
時間枠:baseline and 12 weeks post
baseline and 12 weeks post

二次結果の測定

結果測定
時間枠
病歴
時間枠:ベースライン
ベースライン
Demographic information
時間枠:baseline
baseline
Smoking practices
時間枠:baseline
baseline
Exercise practices
時間枠:baseline and monthly
baseline and monthly
State Anxiety
時間枠:baseline and 12 weeks post
baseline and 12 weeks post
Perceived Stress
時間枠:baseline and 12 weeks post
baseline and 12 weeks post
Depression
時間枠:baseline and 12 weeks post
baseline and 12 weeks post
Sleep - duration and quality
時間枠:baseline and 12 weeks post
baseline and 12 weeks post
Quality of Life as related to asthma
時間枠:baseline and 12 weeks post
baseline and 12 weeks post
Body composition
時間枠:baseline and 12 weeks post
baseline and 12 weeks post
Cardiovascular fitness level- VO2 max
時間枠:baseline and 12 weeks post
baseline and 12 weeks post
Resting Heart Rate
時間枠:baseline and 12 weeks post
baseline and 12 weeks post
Heart Rate Variability and ECG
時間枠:baseline and 12 weeks post
baseline and 12 weeks post
Serum cholesterol levels
時間枠:baseline and 12 weeks post
baseline and 12 weeks post
Fasting blood glucose
時間枠:baseline and 12 weeks post
baseline and 12 weeks post
Cortisol
時間枠:baseline and 12 weeks post
baseline and 12 weeks post
Insulin
時間枠:baseline and 12 weeks post
baseline and 12 weeks post
CRP
時間枠:baseline and 12 weeks post
baseline and 12 weeks post
Homocysteine
時間枠:baseline and 12 weeks post
baseline and 12 weeks post
Lipoprotein-Associated Phospholipase A2 (PLAC)
時間枠:baseline and 12 weeks post
baseline and 12 weeks post
Medication usage
時間枠:prior and throughout study
prior and throughout study
Exercise Adherence
時間枠:throughout study
throughout study
Resting blood pressure
時間枠:baseline and 12 weeks post
baseline and 12 weeks post

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:Kasee J Hildenbrand, PhD、Washington State University

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

2008年9月1日

一次修了 (実際)

2009年5月1日

研究の完了 (実際)

2009年8月1日

試験登録日

最初に提出

2009年1月16日

QC基準を満たした最初の提出物

2009年1月16日

最初の投稿 (見積もり)

2009年1月21日

学習記録の更新

投稿された最後の更新 (見積もり)

2012年1月4日

QC基準を満たした最後の更新が送信されました

2011年12月31日

最終確認日

2011年12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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