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Completed

NCT Number: NCT06472882

Impact of Transcranial Direct Current Stimulation on the Capacity to Perform Burpees

Introduction and Background:

Transcranial direct current stimulation (tDCS) has emerged as a potential intervention to improve physical performance. The primary aim of this study is to investigate the effects of tDCS applied to the primary motor cortex (M1) and dorsolateral prefrontal cortex (DLPFC) on performance in a maximal effort task, specifically the No Jump Burpee exercise.

Study Design:

This study will utilize a double-blind crossover design, where each subject will complete three experimental conditions: a-DLPFC, a-M1, and SHAM.

Participants:

Twenty healthy male subjects will be recruited for the study.

Intervention:

Each participant will undergo three conditions in a randomized order:

a-DLPFC: tDCS applied to the dorsolateral prefrontal cortex.

a-M1: tDCS applied to the primary motor cortex. SHAM: Placebo stimulation.

Procedure:

Prior to performing the No Jump Burpee exercise to exhaustion, tDCS will be administered at a current of 2 milliampere (mA) for 20 minutes.

Measurements:

The following variables will be measured during the exercise:

Total number of repetitions of the No Jump Burpee exercise. Vastus lateralis muscle oxygen saturation. Heart rate. Subjective perception of exertion (RPE).

Data Analysis:

Repeated measures ANOVAs will be used to analyze the effects of the different tDCS conditions on the performance outcomes.

Ethical Considerations:

The study protocol will be reviewed and approved by an appropriate ethics committee. Written informed consent will be obtained from all participants before participation in the study.

Objectives:

The primary objective is to evaluate the impact of tDCS on physical performance, specifically measuring the total number of repetitions of the No Jump Burpee exercise. Secondary objectives include assessing the changes in muscle oxygen saturation, heart rate, and subjective perception of exertion.

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Key information

Conditions

Transcranial Direct Current Stimulation Dorsolateral Prefrontal Cortex Primary Motor Cortex

Age range

18 year–35 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Catholic University of Murcia

Guadalupe, Murcia, 30107, Spain

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy subject.
  • No use of any ergogenic substance.
  • Participants must be recreationally active, defined as engaging in moderate physical activity at least 3 times per week for the past 6 months

Exclusion criteria

  • Any contraindications to transcranial Direct Current Stimulation, such as metallic implants in the head, active implanted medical devices (e.g., pacemakers), or skin conditions affecting the scalp.
  • Current or recent (within the past 6 months) substance abuse, including alcohol or recreational drugs.
  • Musculoskeletal injury within the past 6 weeks.
  • Lower extremity pain above 3 or more according to numeric pain scale.
  • History of epilepsy or convulsive crisis.

Treatment and study plan

tDCS targeting DLPFC

Device

The anodic electrode will be placed on the left DLPFC (area F3) and the cathode on the right orbitofrontal cortex (area Fp2). Participants will receive 20 minutes of tDCS at 2 mA while seated.

tDCS targeting M1

Device

The anodes will be placed over C3 and C4 (according to EEG 10-20 system), and the cathodes over the ipsilateral shoulders. Participants will receive 20 minutes of tDCS at 2 mA while seated.

Sham tDCS

Device

The electrodes will be placed as in the other conditions, but the stimulation will be switched off after 30 seconds, providing an initial stinging sensation without continuous stimulation.

Primary outcomes

  1. Number of "No Jump Burpees" to Exhaustion

    Time frame: Measured immediately at the end of each experimental session (DLPFC, M1, SHAM), approximately 5-10 minutes after the start of the test..

    The primary objective of the study is to measure the number of repetitions of the "No Jump Burpee" exercise that participants can perform until exhaustion. This exercise is performed at a cadence of 20 burpees per minute, and exhaustion is determined when the participant can no longer maintain the correct pace or technique.

Secondary outcomes

  1. Rating of Perceived Exertion (RPE)

    Time frame: Measured every 20 seconds during exercise, from the start until the participant reaches exhaustion, approximately 5-15 minutes per session.

    Assessment of perceived exertion using the Borg CR10 scale, measured every 20 seconds during exercise.

  2. Muscle Oxygen Saturation in the Vastus Lateralis

    Time frame: Measured continuously at a frequency of 1 Hz during the exercise, from the start until the participant reaches exhaustion, approximately 5-15 minutes per session.

    Continuous measurement of muscle oxygen saturation (SmO2) using a near-infrared spectroscopy (NIRS) device.

  3. Heart Rate During Exercise

    Time frame: Measured continuously on a beat-by-beat basis during the exercise, from the start until the participant reaches exhaustion, approximately 5-15 minutes per session.

    Continuous measurement of heart rate during the performance of the "No Jump Burpee" exercise until exhaustion.

Other outcomes

  1. Mood State Before Exercise

    Time frame: Before each experimental session.

    Assessment of mood state using the Profile of Mood States (POMS) before and after each exercise session. The POMS is a psychological rating scale used to assess transient, distinct mood states. The scale consists of 65 items, each rated on a 5-point scale from 0 (Not at all) to 4 (Extremely). The minimum score is 0, and the maximum score is 260. Higher scores indicate a worse mood state.

  2. Anxiety Level Before Exercise

    Time frame: Before each experimental session

    Assessment of anxiety using the Beck Anxiety Inventory (BAI) before each exercise session. The BAI is a 21-item self-report inventory used to measure the severity of an individual's anxiety. Each item is scored on a 4-point scale ranging from 0 (Not at all) to 3 (Severely). The minimum score is 0, and the maximum score is 63. Higher scores indicate higher levels of anxiety.e session.

  3. Sleep Quality on the Night Prior to Exercise

    Time frame: Before each experimental session.

    Assessment of sleep quality using the Pittsburgh Sleep Quality Index (PSQI) before each exercise session. The PSQI is a self-rated questionnaire that assesses sleep quality and disturbances over a 1-month time interval. It consists of 19 items, generating seven component scores that add up to a global score. The global score ranges from 0 to 21, with higher scores indicating worse sleep quality.

Sponsors and collaborators

Lead sponsor

Universidad Católica San Antonio de Murcia

Other

Collaborators

  • University of A Coruna, La Coruna, Spain

Registry information

Official study title

Impact of Transcranial Direct Current Stimulation on the Capacity to Perform Burpees: a Randomized Controlled Trial

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Jun 25, 2024
Registry last updated
Jun 25, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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