Effects of Conditioning Activities in Female Athletes
Effect of Conditioning Activities on Neuromuscular Performance in Female Invasion Sports Athletes
1 other identifier
interventional
20
1 country
1
Brief Summary
This study will investigate how different warm-up strategies affect physical performance in female athletes who practice invasion sports (e.g., soccer, handball, and basketball). Participants will complete three different conditions: a standard warm-up only, a warm-up followed by a performance-enhancing activity, and a warm-up followed by a low-intensity activity designed to simulate the same expectations without real physiological effects. After each condition, athletes will perform tests of vertical jump performance and change-of-direction speed. In addition, participants will report their perceived effort, expectations, muscle soreness, and recovery status. The study will include eighteen female athletes and will be conducted under controlled conditions, including standardized hydration, recovery, and environmental factors. The design will allow comparison of the physical and psychological effects of the different warm-up strategies on performance.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 14, 2026
CompletedFirst Posted
Study publicly available on registry
April 21, 2026
CompletedStudy Start
First participant enrolled
May 10, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
August 20, 2026
Study Completion
Last participant's last visit for all outcomes
November 25, 2026
April 23, 2026
April 1, 2026
3 months
April 14, 2026
April 20, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Countermovement Jump Height
Countermovement jump height (cm), assessed under standardized conditions using a contact mat. Participants will perform three attempts, and the mean value will be used for analysis. Jumps will be executed with hands on hips to minimize upper-body contribution. Measurements will be collected at baseline and after each experimental condition to evaluate changes in performance.
Baseline (pre-intervention) following each experimental condition within the same session.
Secondary Outcomes (2)
Agility Performance
Baseline (pre-intervention) and after the countermovement jump assessment (following each experimental condition).
Participant Expectation
Post-intervention (after each condition).
Study Arms (3)
Conditioning Activity
EXPERIMENTALThe "real" conditioning activity will consist of one set of six repetitions of drop jumps performed at maximal intensity. The box height will be individually determined during two familiarization sessions to ensure optimal performance and safety. Each repetition will be separated by a 15-second interval. Participants will be instructed to step off the box and, upon ground contact, perform the jump as quickly as possible, emphasizing minimal ground contact time and maximal rebound height. Arm swing will be allowed to ensure maximal performance.
Control Condition
ACTIVE COMPARATORIn the control condition, only the standardized warm-up will be performed. However, the total duration will be adjusted to match the other conditions, with no additional intervention. In other words, if the conditioning activity and SHAM conditions last 25 minutes (10 minutes of standardized warm-up + 15 minutes of the conditioning activity itself), in the control condition participants will perform the standardized warm-up repeatedly until reaching 25 minutes.
Sham Condition
SHAM COMPARATORThe SHAM condition will be performed using the free-weight squat with a load of 20% of 1RM, i.e., a "simulated" conditioning activity insufficient to induce physiological effects. Three sets will be performed, with three-minute intervals between them. During these intervals, pneumatic tourniquets (77 × 21.5 cm) will be placed on the proximal portion of the thighs and inflated to (only) 15 mmHg for 3 minutes (including 30 seconds before and after for placement and removal). Movement cadence will be controlled using a metronome, ensuring that participants perform the movement in synchrony with the auditory signal. The adopted cadence will be 20/20, i.e., 2 seconds for the eccentric phase and 2 seconds for the concentric phase, totaling 4 seconds per repetition. Players will receive verbal suggestion that this technique is expected to improve performance with less fatigue compared to the "heavy" exercise, referring to the "real" conditioning activity condition.
Interventions
This study uses a randomized crossover design in which participants complete three conditions (real conditioning activity, SHAM, and control), reducing inter-individual variability. A key feature is the SHAM condition designed to control for placebo and expectancy effects, combining low-load resistance exercise (20% 1RM), verbal suggestion, and simulated blood flow restriction (15 mmHg), insufficient to induce physiological responses. All conditions are strictly standardized, including a warm-up, metronome-controlled cadence, fixed rest intervals, and equal total duration. The conditioning activity (drop jump) is performed at maximal intensity with individualized box height and standardized technique. The study focuses exclusively on female athletes and includes evaluator blinding, addressing gaps in research and improving control of psychophysiological influences on performance.
Eligibility Criteria
You may qualify if:
- Female athletes aged 18 to 30 years
- Familiarity with the proposed tests and exercises
- Ability to perform all testing procedures
- Regular participation in invasion team sports (at least two sessions per week) for a minimum of two years
You may not qualify if:
- Presence of musculoskeletal injuries that could limit test performance
- Injury occurring during the study period
- Absence for more than seven days between experimental sessions
- Failure to comply with the data collection schedule
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Federal University of Triângulo Mineiro
Uberaba, Minas Gerais, 55, Brazil
Related Publications (5)
Ramirez-Campillo R, Andrade DC, Izquierdo M. Effects of plyometric training volume and training surface on explosive strength. J Strength Cond Res. 2013 Oct;27(10):2714-22. doi: 10.1519/JSC.0b013e318280c9e9.
PMID: 23254550RESULTXu K, Blazevich AJ, Boullosa D, Ramirez-Campillo R, Yin M, Zhong Y, Tian Y, Finlay M, Byrne PJ, Cuenca-Fernandez F, Wang R. Optimizing Post-activation Performance Enhancement in Athletic Tasks: A Systematic Review with Meta-analysis for Prescription Variables and Research Methods. Sports Med. 2025 Apr;55(4):977-1008. doi: 10.1007/s40279-024-02170-6. Epub 2025 Jan 24.
PMID: 39853660RESULTSeitz LB, de Villarreal ES, Haff GG. The temporal profile of postactivation potentiation is related to strength level. J Strength Cond Res. 2014 Mar;28(3):706-15. doi: 10.1519/JSC.0b013e3182a73ea3.
PMID: 23965945RESULTBoullosa D, Beato M, Dello Iacono A, Cuenca-Fernandez F, Doma K, Schumann M, Zagatto AM, Loturco I, Behm DG. A New Taxonomy for Postactivation Potentiation in Sport. Int J Sports Physiol Perform. 2020 Aug 19;15(8):1197-1200. doi: 10.1123/ijspp.2020-0350.
PMID: 32820135RESULTBlazevich AJ, Babault N. Post-activation Potentiation Versus Post-activation Performance Enhancement in Humans: Historical Perspective, Underlying Mechanisms, and Current Issues. Front Physiol. 2019 Nov 1;10:1359. doi: 10.3389/fphys.2019.01359. eCollection 2019.
PMID: 31736781RESULT
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Gustavo Ribeiro da Mota, PhD
Federal University of Triângulo Mineiro
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Full Professor (PhD)
Study Record Dates
First Submitted
April 14, 2026
First Posted
April 21, 2026
Study Start (Estimated)
May 10, 2026
Primary Completion (Estimated)
August 20, 2026
Study Completion (Estimated)
November 25, 2026
Last Updated
April 23, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared due to privacy and confidentiality considerations. The dataset is small and may allow participant identification.