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临床试验/NCT07296640
NCT07296640
已完成
不适用

A Prospective, Single-Center, Interventional Study to Evaluate the 5-Line Principle of Balanced Intensity Training (BPIT) for Enhancing Physical Performance and Reducing Injury Risk

MMSx Authority Institute for Movement Mechanics & Biomechanics Research Inc.1 个研究点 分布在 1 个国家目标入组 23 人开始时间: 2024年7月1日最近更新:

概览

阶段
不适用
状态
已完成
发起方
MMSx Authority Institute for Movement Mechanics & Biomechanics Research Inc.
入组人数
23
试验地点
1
主要终点
Change in 1RM Strength

概览

简要总结

This prospective, single-center, interventional pilot (n=23) evaluates the 5-Line Principle of Balanced Intensity Training (BPIT) over 6 weeks at GFFI Fitness Academy. Participants (18 males aged 22-48, 5 females aged 20-33) will receive BPIT 5-Line Training (3 sessions/week, 6 weeks). No control group. Conducted July 1 - November 30, 2024.

Progressive intensity via anatomical lines: 1. Ground-Based (Low Intensity); 2. Knee-Level (Low-Moderate); 3. Standing (Moderate); 4. Head-Level (Moderate-High); 5. Plyometric/High-Impact (High). Aims to assess changes in strength, HRV, and injury risk.

详细描述

STUDY DESIGN: Prospective, single-center, interventional pilot (n=23) with single-group assignment. All participants receive the BPIT 5-Line intervention. Assessments at baseline and Week 6.

INTERVENTION: BPIT 5-Line Training: 3 x 60-minute sessions/week for 6 weeks, progressing across five intensity lines: 1. Ground-Based (Low Intensity, e.g., prone planks); 2. Knee-Level (Low-Moderate, e.g., shoulder press); 3. Standing (Moderate, e.g., half-squat); 4. Head-Level (Moderate-High); 5. Plyometric/High-Impact (High Intensity). Specific exercises detailed in Training Protocol Manual.

OBJECTIVES: Primary - Evaluate BPIT's impact on 1RM strength (e.g., squat, bench press, deadlift) and training-related injury incidence. Secondary - Assess changes in HRV (RMSSD), HRR (bpm in 60s), EMG muscle activation, joint biomechanics (knee valgus, spinal curvature), adherence (% sessions completed), and participant feedback (questionnaires).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
22 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy adults aged 22-65 years
  • Regular fitness trainees (≥2 sessions/week prior)
  • Able to provide informed consent
  • No recent musculoskeletal injury (past 3 months)

排除标准

  • \- Cardiovascular disease or uncontrolled hypertension
  • Current musculoskeletal injury or surgery (past 6 months)
  • Neurological disorders affecting movement
  • Pregnancy
  • Use of performance-enhancing substances

结局指标

主要结局

Change in 1RM Strength

时间窗: 6 weeks

Change in one-repetition maximum (1RM) strength for key exercises (e.g., squat, bench press) from baseline to week 6. Measured in kilograms (kg) using standard 1RM testing protocol. Time Frame: Baseline to Week 6 Unit of Measure: kilograms (kg)

Injury Incidence

时间窗: Baseline to Week 6

Number of new musculoskeletal injuries reported during the study period, defined as any complaint requiring medical attention, training modification, or rest exceeding 1 day. Measured as incidence rate per 100 participant-weeks (normalized for exposure in this 23-participant pilot). Unit of Measure: injuries per 100 participant-weeks

次要结局

  • Change in Heart Rate Variability (HRV)(Week 6)
  • Change in Muscle Activation (EMG Amplitude)(Baseline to Week 6)
  • Change in Joint Biomechanics (Knee Valgus and Spinal Curvature)(Baseline to Week 6)
  • Training Adherence(Baseline to Week 6)
  • Participant Feedback(6 weeks)
  • Heart Rate Recovery (HRR)(6 Weeks)

研究者

发起方
MMSx Authority Institute for Movement Mechanics & Biomechanics Research Inc.
申办方类型
Other
责任方
Sponsor

研究点 (1)

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