NCT07855406

Brief Summary

This study investigates how physical fatigue, cognitive fatigue, and a combination of both affect reaction time and depth perception in adolescents. Sixty healthy adolescents will participate in four experimental conditions: a control condition, a physical fatigue condition, a cognitive fatigue condition, and a combined fatigue condition. Physical fatigue will be induced using a modified shuttle run protocol, while cognitive fatigue will be induced using computerized Stroop and mental arithmetic tasks. Reaction time will be assessed using the BlazePod system, and depth perception will be evaluated using the Titmus Fly Stereotest before and after each condition. Heart rate, perceived exertion, and mental fatigue will also be measured to verify the effectiveness of the fatigue protocols. The findings may improve understanding of how different types of fatigue influence perceptual and motor performance in adolescents and may contribute to the development of safer and more effective training and sport participation strategies.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Apr 2026

Shorter than P25 for not_applicable

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 21, 2026

Completed
10 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 31, 2026

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

September 28, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

October 2, 2026

Completed
Last Updated

October 2, 2026

Status Verified

September 1, 2026

Enrollment Period

2 months

First QC Date

September 28, 2026

Last Update Submit

September 28, 2026

Conditions

Keywords

fatiguereaction timedepth perceptioncognitive performancepsychomotor performance

Outcome Measures

Primary Outcomes (2)

  • Reaction Time

    Reaction time will be assessed using the BlazePod wireless light-based system. Reaction time will be recorded in milliseconds as the latency between stimulus presentation and participant response. Two trials will be performed, and the best performance will be used for analysis.

    Immediately before and immediately after each experimental condition.

  • Depth Perception

    Depth perception will be assessed using the Titmus Fly Stereotest. Stereopsis will be expressed in arc seconds, with lower values indicating better depth perception performance. Two trials will be conducted at each measurement point, and the lowest value will be used for analysis.

    Immediately before and immediately after each experimental condition.

Secondary Outcomes (3)

  • Heart Rate

    Immediately before and immediately after each experimental condition.

  • Rating of Perceived Exertion (RPE)

    Perceived exertion will be assessed using the Borg CR-20 Scale before and after each experimental condition to evaluate subjective fatigue levels.

  • Mental Fatigue Scale Score

    Immediately before and immediately after each experimental condition.

Study Arms (4)

Control Condition

EXPERIMENTAL

Participants completed the testing procedures without exposure to any physical or cognitive fatigue protocol. Reaction time and depth perception were assessed before and after the control condition.

Other: Control Condition

Physical Fatigue Condition

EXPERIMENTAL

Participants completed a 16-minute modified 20-meter shuttle run protocol designed to induce physical fatigue. Reaction time and depth perception were assessed before and after the protocol.

Behavioral: Physical Fatigue Protocol

Cognitive Fatigue Condition

EXPERIMENTAL

Participants completed a 16-minute cognitive fatigue protocol consisting of an 8-minute Stroop task and an 8-minute mental arithmetic task. Reaction time and depth perception were assessed before and after the protocol.

Behavioral: Cognitive Fatigue Protocol

Combined Fatigue Condition

EXPERIMENTAL

Participants completed a combined fatigue protocol consisting of 8 minutes of a modified shuttle run followed by 4 minutes of a Stroop task and 4 minutes of a mental arithmetic task. Reaction time and depth perception were assessed before and after the protocol.

Behavioral: Combined Fatigue Protocol

Interventions

A 16-minute modified 20-meter shuttle run protocol designed to induce physical fatigue through progressively increasing running intensity.

Physical Fatigue Condition

A 16-minute computerized protocol consisting of Stroop and mental arithmetic tasks designed to induce cognitive fatigue.

Cognitive Fatigue Condition

A protocol combining physical and cognitive fatigue tasks, including a modified shuttle run, Stroop task, and mental arithmetic task.

Combined Fatigue Condition

Participants completed the testing procedures without exposure to any physical or cognitive fatigue protocol.

Control Condition

Eligibility Criteria

Age14 Years - 18 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Adolescents aged 14 to 18 years.
  • Male or female participants.
  • Normal or corrected-to-normal vision.
  • Ability to understand and follow study procedures.
  • Written informed consent from both the participant and a parent/legal guardian.

You may not qualify if:

  • History of neurological disorders.
  • Visual disorders affecting depth perception.
  • Orthopedic injuries or musculoskeletal conditions limiting physical activity.
  • Any medical condition that would contraindicate participation in physical exercise.
  • Failure to complete all experimental sessions.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Konya

Konya, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Fatigue

Condition Hierarchy (Ancestors)

Signs and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Ahmet Kaan ASLAN, PhD

    Gazi University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
Blinding was not feasible because participants and investigators were aware of the fatigue condition being administered. The physical and cognitive fatigue protocols were readily identifiable, making masking impractical.
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Model Details: This study uses a counterbalanced within-subject crossover design. Each participant completes four experimental conditions (control, physical fatigue, cognitive fatigue, and combined fatigue) in a randomized counterbalanced order. A minimum 24-hour washout period is provided between sessions to minimize carryover effects. Reaction time and depth perception are assessed immediately before and after each condition, allowing each participant to serve as their own control.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr. Ahmet Kaan ASLAN

Study Record Dates

First Submitted

September 28, 2026

First Posted

October 2, 2026

Study Start

April 1, 2026

Primary Completion

May 21, 2026

Study Completion

May 31, 2026

Last Updated

October 2, 2026

Record last verified: 2026-09

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be made publicly available. Data contain information collected from adolescent participants, and sharing is restricted to protect participant confidentiality and privacy.

Locations