NCT07307963

Brief Summary

The purpose of this study is to determine whether load-velocity (L-V) relationship variables (L0, v0, and Aline) are sensitive indicators of fatigue produced by different squat fatigue protocols. The study aims to answer how accurately these L-V measures reflect changes in performance, particularly changes in one-repetition maximum (1RM), after varying levels of induced fatigue. Twenty-eight resistance-trained men completed three sessions involving different fatigue protocols or no training. L-V variables measured before and after each protocol were compared. The findings will help determine whether L-V relationship parameters can be used as practical and sensitive tools for monitoring fatigue during resistance training.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
28

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started May 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

May 5, 2024

Completed
5 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 10, 2024

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 10, 2024

Completed
1.1 years until next milestone

First Submitted

Initial submission to the registry

November 27, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

December 29, 2025

Completed
Last Updated

December 29, 2025

Status Verified

December 1, 2025

Enrollment Period

5 days

First QC Date

November 27, 2025

Last Update Submit

December 19, 2025

Conditions

Keywords

resistance trainingfatiguevelocity-based training

Outcome Measures

Primary Outcomes (1)

  • Change in Theoretical Maximal Load (L0) Derived From the Load-Velocity Relationship

    Difference in theoretical maximal load (L0, kg) derived from the load-velocity relationship between baseline (pre-session) and immediately post-session incremental loading tests.

    Baseline (pre-session) and immediately post-session (within 15 minutes)

Secondary Outcomes (3)

  • Change in Theoretical Maximal Velocity (v0) Derived From the Load-Velocity Relationship

    Baseline (pre-session) and 15 minutes post-session

  • Change in Area Under the Load-Velocity Relationship Line (Aline)

    Baseline (pre-session) and immediately post-session (within 15 minutes)

  • Change in One-Repetition Maximum (1RM) in the Smith-Machine Squat

    Baseline (pre-session) and immediately post-session (within 15 minutes)

Study Arms (3)

Control Condition

Control Protocol Arm: Participants completed no exercise between the pre- and post-session load-velocity tests.

Other: Control Protocol (No Training)

Moderate-Fatigue Protocol

Participants performed 5 sets of the Smith-machine squat at 70% of their 1RM, completing half of the maximum possible number of repetitions in each set. This protocol was designed to induce a moderate level of fatigue while avoiding complete muscular failure.

Other: Moderate-fatigue

High-Fatigue Protocol

In the high-fatigue protocol, participants performed five sets of Smith-machine squats at 70% of their 1RM, completing each set to muscular failure. In every set, participants continued lifting until they could no longer complete a full repetition with proper technique. This protocol was designed to induce a high level of neuromuscular fatigue and to test the sensitivity of load-velocity variables under maximal fatigue conditions.

Other: High-fatigue

Interventions

This intervention consists of no training or exercise during the session. Participants assigned to the control arm rest for the entire duration between the pre-session and post-session load-velocity assessments. No fatigue-inducing activity, resistance exercise, or additional intervention is administered, allowing all observed changes to reflect normal variation without training-related fatigue.

Control Condition

Participants performed five sets of Smith-machine squats at 70% of their 1-repetition maximum (1RM), completing half of the maximum possible repetitions in each set. This protocol was designed to induce a moderate level of neuromuscular fatigue without reaching complete exhaustion.

Moderate-Fatigue Protocol

This intervention involves no training or fatigue-inducing activity. Participants do not perform any squat sets between the pre- and post-session incremental loading tests. This condition serves as a baseline to determine natural variations in load-velocity measures, thereby eliminating the influence of exercise-induced fatigue.

High-Fatigue Protocol

Eligibility Criteria

Age18 Years - 35 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

Twenty-eight physically trained males, with an average age of 23.3 years (standard deviation \[SD\]: 3.0 years; range: 20-36 years), willingly enrolled in this research endeavor. The participants exhibited a mean body mass of 78.1 kg (SD: 9.3 kg), a body height of 177.2 cm (SD: 3.3 cm), and a one-repetition maximum (1RM) for smith-machine squat (SMS) exercise of 150.9 kg (SD: 12.5 kg). All subjects possessed prior RT experience, averaging 5.0 years (SD: 2.6 years), and demonstrated proficiency in executing the SMS exercise during the familiarization session.

You may qualify if:

  • Healthy males aged 18-40 years.
  • Resistance-trained (minimum 2 years of regular lower-body resistance training and ≥2 sessions/week).
  • Able to perform a proper smith-machine back squat with correct technique.
  • RM smith-machine squat measurable and ≥ bodyweight (or specify threshold used in study).
  • No musculoskeletal injury of lower limbs or back in the past 6 months.
  • Not using performance-enhancing drugs or anabolic steroids for the past 12 months.
  • Willing and able to attend all testing and training sessions and provide written informed consent.

You may not qualify if:

  • Any cardiovascular, pulmonary, metabolic, or neurological disease contraindicating intense exercise.
  • Recent (≤6 months) lower-extremity or spinal surgery or acute injury.
  • Current musculoskeletal pain or injury that limits squat performance.
  • Use of medications that affect neuromuscular performance (e.g., systemic corticosteroids) or stimulant drugs.
  • Regular participation in structured lower-body rehabilitation programs.
  • Failure to complete familiarization or preliminary 1-RM testing.
  • Inability or unwillingness to provide informed consent or follow study procedures.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

İstanbul Gelişim Üniversity

Istanbul, avcılar, 34310, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Fatigue

Condition Hierarchy (Ancestors)

Signs and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Deniz Şentürk, PhD

    Istanbul Gelisim University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CROSSOVER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor, PhD

Study Record Dates

First Submitted

November 27, 2025

First Posted

December 29, 2025

Study Start

May 5, 2024

Primary Completion

May 10, 2024

Study Completion

October 10, 2024

Last Updated

December 29, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will share

Individual participant data (IPD) will be shared after de-identification. Data will be available to qualified researchers upon reasonable request for academic purposes. Access will be provided following publication of the primary results. Researchers will be required to submit a brief proposal describing the intended use of the data, and data will be shared through secure, controlled access. No identifiable information will be released.

Shared Documents
STUDY PROTOCOL, SAP, ICF, CSR
Time Frame
Individual participant data and supporting documents will become available 6 months after publication of the study results and will remain available for 5 years.
Access Criteria
Individual participant data (IPD) will be shared in anonymized form with qualified researchers for scientific purposes. The shared data will include de-identified performance measurements, load-velocity variables, and outcome measures relevant to the study.
More information

Locations