Individual Response to Different Volumes of Resistance Training
Determinants of Intra-individual Variation in Adaptability to Resistance Training of Different Volumes
The literature is not clear as to which training volume to employ during initial phases of resistance training programs to ensure optimal muscular adaptations. The purpose of this study is therefore to compare effects of strength training with low versus moderate volume on muscular function and hypertrophy in previously untrained, healthy individuals. Furthermore, the investigators will relate individual variation in responses to proxy markers of individual training state, such as baseline muscular function and muscle fiber type.
The study will include 25 women and 25 men and will consist of a 12-week resistance training protocol. Each study participant will act as their own control, performing both the low- (1-set) and the moderate-volume (3-sets) protocol, allocated to either the dominant or non-dominant leg, in a stratified and randomized fashion.
Primary outcome measures are thigh muscle cross section area and unilateral knee extension strength. Additionally, muscle fiber type composition will be evaluated as well as additional parameters of muscular function.
The primary hypothesis is that low-volume protocols will be beneficial for individuals with glycolytic muscle phenotypes, whereas the opposite will be true for individuals with more aerobic phenotypes.
調査の概要
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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-
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Lillehammer、ノルウェー
- Lillehammer University College
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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:
- Healthy
- Non-smoking
- Able to tolerate resistance exercise training
Exclusion Criteria:
- Presence or history of cardiovascular, metabolic, endocrine or neuromuscular disease
- Diagnosed mental health disorder
- Intolerance to local anesthetic
- No experience with exercise training
- Performing regular resistance training (more than 1 session per week during last 12 months)
- Impaired strength/ neuromuscular function due to previous injury
- Recurrent pain in lower back, knee or shoulders
- Taking prescribed medication that may affect outcome of training intervention
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：基礎科学
- 割り当て：なし
- 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 |
|---|---|
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実験的：Arm label 1-Set, 3-Set
12-week progressive strength training protocol of different volumes
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Every study participant will complete 12 weeks of progressive strength training with one leg performing 1-set per exercise per session and the contralateral leg performing 3-sets per exercise per session.
Allocation of dominant/non-dominant leg to either 1- or 3-set protocol will be done in a stratified, randomized fashion (stratified with regard to sex and baseline strength).
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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 |
|---|---|---|
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Thigh muscle cross-sectional area
時間枠：Week 0 (baseline) and 12 (post training intervention)
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Changes in muscle cross sectional area of each thigh from baseline to post intervention, assessed by MRI.
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Week 0 (baseline) and 12 (post training intervention)
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Unilateral knee-extension isometric strength
時間枠：Week 0 (baseline), 2, 5, 9 (during intervention) and 12 (after training intervention)
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Time course changes in maximum knee extensor, isometric strength evaluated at 120° knee angle (180° fully extended).
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Week 0 (baseline), 2, 5, 9 (during intervention) and 12 (after training intervention)
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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 |
|---|---|---|
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Muscle strength
時間枠：Week 0 (baseline), 2, 5, 9 (during intervention) and 12 (after training intervention)
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Time course changes in maximum isoinertial strength defined by one-repetition maximum in leg press, knee extension, knee flexion, and bench press.
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Week 0 (baseline), 2, 5, 9 (during intervention) and 12 (after training intervention)
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Knee extensors and flexors force-velocity relationship
時間枠：Week 0 (baseline), 2, 5, 9 (during intervention) and 12 (after training intervention)
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Time course changes in torque measured during maximal voluntary isokinetic contraction at 60°, 120° and 240° ∙ sec-1.
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Week 0 (baseline), 2, 5, 9 (during intervention) and 12 (after training intervention)
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Blood hormonal profiles
時間枠：Week 0 (baseline), 2 and 12 (post training intervention)
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Resting (week 0, 2 and 12) and acutely exercise-induced (week 2) hormonal profiles (testosterone, insulin-like growth factor 1, growth hormone and cortisol) determined in serum from venous blood samples.
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Week 0 (baseline), 2 and 12 (post training intervention)
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Muscle fiber cross-sectional area
時間枠：Week 0 (baseline), 2 and 12 (post training intervention)
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Changes in muscle fiber cross-sectional area assessed by immunohistochemistry from muscle biopsy.
Determined from muscle biopsy samples (Vastus lateralis).
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Week 0 (baseline), 2 and 12 (post training intervention)
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Protein expression
時間枠：Week 0 (baseline), 2 and 12 (post training intervention)
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Changes in relative abundance of contractile protein isoforms (myosin heavy chain).
Modification of proteins related to muscle hypertrophy in relation to an acute exercise session (assessed during week 2 of the intervention).
Determined from muscle biopsy samples (Vastus lateralis).
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Week 0 (baseline), 2 and 12 (post training intervention)
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Gene expression
時間枠：Week 0 (baseline), 2 and 12 (post training intervention)
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Changes in gene expression related to skeletal muscle hypertrophy and structural phenotype measured in steady state conditions (biopsy sampled in resting conditions, week 0, 2 and 12) and in relation to acute exercise (biopsy sampled 1-h after strength exercise, week 2).
Determined from muscle biopsy samples (Vastus lateralis).
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Week 0 (baseline), 2 and 12 (post training intervention)
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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 |
|---|---|---|
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Body composition changes
時間枠：Week 0 (baseline) and 12 (post training intervention)
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Changes in body compositions (lean mass and fat mass) from prior intervention to after intervention assessed by dual x-ray absorptiometry scan.
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Week 0 (baseline) and 12 (post training intervention)
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Habitual physical activity
時間枠：Week 0
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Self-reported prior habitual physical activity assessed by questionnaire and interview before training intervention
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Week 0
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Daily nutrient intake
時間枠：Week 6
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Daily nutrient intake assessed by a 4-day food intake registration.
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Week 6
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協力者と研究者
捜査官
- 主任研究者：Stian Ellefsen, PhD、Inland Norway University of Applied Sciences
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
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 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
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
キーワード
その他の研究ID番号
- Trainsome 2014#002
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。