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Multifactorial Modeling and Intelligent Intervention Strategies for Individual Differences in Post-activation Performance Enhancement (PAPE) Responses

Multifactorial Modeling and Intelligent Intervention Strategies for Individual Differences in Post-Acute Enhancement Activation (PAPE) Responses

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124780
Enrollment
Unknown
Registered
2026-05-18
Start date
2026-05-23
Completion date
Unknown
Last updated
2026-05-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None

Interventions

Control Group:Subjects completed a standardized warm-up, a specific conditioning activity (CA), and countermovement jump (CMJ) tests at multiple time points under experimental conditions. The standard
subsequently, a standardized dynamic warm-up sequence focusing on mobilization and activation of major lower limb joints and muscle groups, including knee-to-chest calf raises, four-way squats, foot c
Experimental Group:Subjects completed a standardized warm-up, a specific conditioning activity (CA), and countermovement jump (CMJ) tests at multiple time points under experimental conditions. The sta
subsequently, a standardized dynamic warm-up sequence focusing on mobilization and activation of major lower limb joints and muscle groups, including knee-to-chest calf raises, fo

Sponsors

Beijing Sport University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Age 18–35 years, 100 males and 100 females, totaling 200 participants. 2. Physically healthy, with no Explicit cardiovascular, respiratory, neuromuscular, musculoskeletal system diseases, or other medical conditions or health issues that would render them unsuitable for exercise testing. 3. Possess a certain level of exercise foundation, enabling them to safely complete standardized warm-up, specific conditioning activities (CA), countermovement jumps (CMJ), and other tests under the guidance of researchers. 4. Willing to complete the entire experimental protocol as required by the study, including two laboratory visits for testing and completion of relevant questionnaires and record forms. 5. Voluntarily participate in this study and have signed a written informed consent form. 6. Able to control recent training, sleep, caffeine intake, alcohol consumption, smoking, and other related behaviors as required prior to testing. 7. Participants may have diverse exercise backgrounds and training experiences, including but not limited to different sport-specific participation histories, training duration, training frequency, training continuity, length of training hiatus, and current physical activity levels. This study allows for and focuses on individual variability arising from differences in exercise background. However, all participants must possess basic motor abilities, action comprehension abilities, and experimental cooperation abilities to safely complete all tests and intervention protocols specified in this study.

Exclusion criteria

Exclusion criteria: 1. Presence of diseases affecting the cardiovascular system, respiratory system, neuromuscular system, or musculoskeletal system; recent exercise-related injuries, pain; or other health issues that may impact test safety or result interpretation. 2. Use of medications, supplements, or other interventions that may affect neural excitability, heart rate response, muscle function, or exercise performance. 3. Significant intolerance or contraindications to study-related experimental conditions, such as sensitivity or intolerance to caffeine, or other situations unsuitable for exposure to the corresponding experimental conditions. 4. Failure to control sleep, training, diet, caffeine intake, alcohol consumption, smoking, or other relevant behaviors as required prior to the experiment. 5. Inability to understand experimental requirements, inability to cooperate in completing the prescribed procedures, or researcher judgment that the individual is not capable of safely completing the study's tests and interventions. 6. Occurrence of significant discomfort, adverse reactions, injury, withdrawal during the experiment, or failure to complete key testing procedures. 7. Severe missing data that prevents inclusion in subsequent statistical analysis. 8. Other situations deemed unsuitable for inclusion in the study by the researcher.

Design outcomes

Primary

MeasureTime frame
Changes in Countermovement Jump (CMJ) Height at Various Time Points;PAPE Optimal Increment (?best);PAPE Optimal Response Time Point (Tbest);PAPE Average Growth Rate / Area Under the Curve;

Secondary

MeasureTime frame
Subjective Effort Sensation at Various Time Points (RPE);Heart rates at various time points;Squat 1RM;Body composition (DEXA);Long-term Background and Status-related Questionnaire Indicators;Circumference and Lower Limb Morphological Indices;Candidate SNP Genotyping Indicators;

Countries

China

Contacts

Public ContactJiaxuan Sun

Beijing Sport University

15637320091@163.com+86 156 3732 0091

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 30, 2026