Tämä sivu käännettiin automaattisesti, eikä käännösten tarkkuutta voida taata. Katso englanninkielinen versio lähdetekstiä varten.

Safety and Acute Effects of tDCS on Vocal Performance in Adolescent Singers

keskiviikko 7. lokakuuta 2026 päivittänyt: Frederico Barreto Kochem, Centro Universitário Augusto Motta

Safety, Tolerability, and Acute Effects of Transcranial Direct Current Stimulation on Vocal Performance in Adolescent Singers Aged 12 to 16 Years: A Randomized Sham-Controlled Proof-of-Concept Study

This randomized, sham-controlled proof-of-concept study aims to investigate the safety, tolerability, and acute effects of transcranial direct current stimulation (tDCS) on vocal performance in adolescent singers aged 12 to 16 years. Twenty-four participants will be randomly assigned in a 1:1 ratio to active or sham tDCS. Active stimulation will consist of 2.0 mA anodal tDCS applied for 20 minutes using 5 × 7 cm electrodes, with the anode positioned over C5 to target the left laryngeal primary motor cortex and the cathode over the right supraorbital region. Participants will perform the same standardized vocal piece before stimulation, immediately after stimulation, and approximately two hours after stimulation. Vocal performances will be audiovisually recorded and evaluated by blinded expert raters using an adapted analytical vocal-performance rubric based on Gynnild (2015). Safety and tolerability will be monitored using a structured symptom checklist and predefined stopping criteria. Self-rated vocal performance, nervousness, confidence, blinding, and protocol feasibility will also be explored.

Tutkimuksen yleiskatsaus

Tila

Ei vielä rekrytointia

Ehdot

Interventio / Hoito

Yksityiskohtainen kuvaus

This randomized parallel-group pilot study will evaluate the safety, tolerability, and acute effects of transcranial direct current stimulation (tDCS) in adolescent singers aged 12 to 16 years.

Twenty-four participants will be allocated in a 1:1 ratio to active or sham stimulation. Active tDCS will be delivered in a single session at 2.0 mA for 20 minutes using 5 × 7 cm electrodes, with the anode positioned over C5 to target the left laryngeal primary motor cortex and the cathode positioned over the right supraorbital region. The sham condition will use the same electrode montage and overall session duration and will reproduce the initial sensations associated with stimulation without sustained current delivery.

Participants will perform the same standardized vocal piece, "Repousa Participants will perform the same standardized vocal piece, "Repousa tranquillo, O meigo Jesus (Lullaby for Baby Jesus)," a traditional Brazilian song listed in ABRSM Singing Grade 2, List A, in G minor, arranged by Hargest Jones and published in Songs of Christmas (Boosey & Hawkes), at baseline, immediately after stimulation, and approximately two hours after stimulation. Performances will be audiovisually recorded, pseudonymized, randomized, and evaluated by blinded expert raters using an adapted analytical vocal-performance rubric based on Gynnild (2015). The rubric evaluates Technique, Language/Text, Musicality, Ability to Communicate, and Choice of Repertoire using grades A through F converted to numerical values from 5 to 0. Because repertoire is standardized by the protocol, the Choice of Repertoire domain will not contribute to the primary vocal-performance score.

Safety and tolerability will be assessed throughout the session and during follow-up using a structured symptom checklist and predefined stopping criteria. Participants will also provide brief 0-10 ratings of nervousness, confidence, and self-perceived vocal performance. These measures are exploratory and are not intended for psychological diagnosis. The study will additionally assess the effectiveness of blinding and the feasibility of conducting a controlled tDCS protocol in adolescent singers.

Written informed consent from a legal guardian and written assent from the adolescent will be obtained before any study procedure. Participation is voluntary and will not influence grades, artistic selection, scholarships, or continued participation in any musical program.

Opintotyyppi

Interventio

Ilmoittautuminen (Arvioitu)

24

Vaihe

  • Ei sovellettavissa

Yhteystiedot ja paikat

Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.

Opiskeluyhteys

Opiskelupaikat

    • Rio de Janeiro
      • Rio de Janeiro, Rio de Janeiro, Brasilia, 21042-432
        • Orquestra Maré do Amanhã
        • Päätutkija:
          • Frederico Barreto Kochem, PT, PhD
        • Päätutkija:
          • Débora Cristina Lima da Silva, PT, PhD
        • Alatutkija:
          • Ricardo Galhardoni, PhD
        • Alatutkija:
          • Renato Santos de Almeida, PT, PhD
        • Ottaa yhteyttä:
        • Alatutkija:
          • Rômulo de Freitas Santos Nicolai, BMus (Classical Voice), MMus

Osallistumiskriteerit

Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.

Kelpoisuusvaatimukset

Opintokelpoiset iät

12 vuotta - 16 vuotta (Lapsi)

Hyväksyy terveitä vapaaehtoisia

Joo

Sukupuolet, jotka voivat opiskella

Kaikki

Kuvaus

Inclusion Criteria:

  • Age 12 to 16 years, inclusive, at the time of enrollment.
  • Regular participation in vocal music training for at least 12 months.
  • Ability to safely perform the standardized vocal piece selected for the study.
  • General health status compatible with participation, confirmed through a pre-session safety screening.
  • No known neurological or clinical condition considered to increase the risk associated with stimulation.
  • No current use of medication or substances considered by the study team to substantially alter cortical excitability or increase procedural risk.
  • Written informed consent from a legal guardian.
  • Written assent from the adolescent and voluntary willingness to participate.

Exclusion Criteria:

  • History of epilepsy or non-febrile seizures.
  • Relevant brain injury, previous cranial surgery, or other neurological condition considered incompatible with the protocol.
  • Pacemaker, implanted electronic device, neurostimulator, or cranial metallic implant that could pose a risk or interfere with stimulation.
  • Current use of anticonvulsant medication or other medication considered by the study team to represent a contraindication or unacceptable precaution.
  • Previous experience with tDCS when such experience could compromise blinding.
  • Dermatitis, wounds, infection, burns, significant pain, or other scalp abnormalities at the planned electrode sites.
  • Known or suspected pregnancy, as a precaution; pregnancy testing will not be performed as part of the study.
  • Acute illness or relevant symptoms on the day of the session, including fever, significant headache, persistent dizziness, relevant sleep deprivation, or acute upper respiratory symptoms when these findings justify postponement or exclusion for safety or performance-related reasons.

Opintosuunnitelma

Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.

Miten tutkimus on suunniteltu?

Suunnittelun yksityiskohdat

  • Ensisijainen käyttötarkoitus: Muut
  • Jako: Satunnaistettu
  • Inventiomalli: Rinnakkaistehtävä
  • Naamiointi: Kolminkertaistaa

Aseet ja interventiot

Osallistujaryhmä / Arm
Interventio / Hoito
Kokeellinen: Active tDCS

Participants will receive a single 20-minute session of active transcranial direct current stimulation (tDCS) at 2.0 mA using 5 × 7 cm electrodes, with the anode positioned over C5 to target the left laryngeal primary motor cortex and the cathode positioned over the right supraorbital region.

Participants will receive a single session of active transcranial direct current stimulation (tDCS). The anode will be positioned over C5, targeting the left laryngeal primary motor cortex, and the cathode over the right supraorbital region using 5 × 7 cm electrodes. Current will be gradually increased to 2.0 mA, maintained for 20 minutes, and gradually reduced at the end of stimulation.

Huijausvertailija: Sham tDCS

Participants will receive a single 20-minute sham tDCS session using the same electrode montage as the active condition. Sham stimulation will reproduce the initial sensations associated with tDCS through an initial ramp-up and brief stimulation period, without sustained current delivery.

Participants will receive a single sham transcranial direct current stimulation (tDCS) session using the same electrode montage as the active condition, with the anode positioned over C5 and the cathode over the right supraorbital region using 5 × 7 cm electrodes. An initial ramp-up and brief stimulation period will reproduce the initial sensations associated with tDCS, followed by discontinuation of sustained current. The sham session will have the same overall duration as the active session.

Mitä tutkimuksessa mitataan?

Ensisijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Incidence and Severity of Treatment-Emergent Adverse Events Associated With Transcranial Direct Current Stimulation
Aikaikkuna: Baseline (pre-stimulation); during the 20-minute stimulation session; immediately post-stimulation; 2 hours post-stimulation; and approximately 24 hours post-stimulation.

Treatment-emergent adverse events will be assessed using a structured checklist documenting the presence and intensity of tingling/itching, warmth or burning sensation, skin redness, headache, dizziness, nausea, fatigue or drowsiness, visual symptoms, and other spontaneously reported symptoms. Symptoms present at baseline will be recorded, and an event will be considered treatment-emergent if it occurs after the start of stimulation or increases in intensity relative to baseline.

For each event, severity will be categorized as none, mild, moderate, or severe. Stimulation interruptions, inability to complete the stimulation session, and adverse events requiring additional assessment or care will also be recorded. The number and proportion of participants experiencing each treatment-emergent adverse event, together with its severity, will be reported.

Baseline (pre-stimulation); during the 20-minute stimulation session; immediately post-stimulation; 2 hours post-stimulation; and approximately 24 hours post-stimulation.
Change in Vocal Performance Scores
Aikaikkuna: Baseline, immediately after intervention, and 2 hours after intervention

Vocal performances will be audiovisually recorded and evaluated by blinded independent expert raters using an adapted analytical vocal-performance rubric based on Gynnild (2015). The rubric evaluates Technique, Language/Text, Musicality, Ability to Communicate, and Choice of Repertoire. Performance grades range from A to F and are converted to numerical values from 5 to 0, with higher scores indicating better vocal performance. Because all participants perform the same standardized repertoire, the Choice of Repertoire domain will not contribute to the primary performance score. The primary vocal-performance score will be calculated as the mean of the four applicable domain scores (Technique, Language/Text, Musicality, and Ability to Communicate), each scored from 0 to 5, resulting in an overall mean score ranging from 0 to 5. Higher scores indicate better vocal performance. Changes over time will be compared between the active and sham groups.

Baseline, immediately after intervention, and 2 hours after intervention
Change in Vocal Performance Scores
Aikaikkuna: Baseline, immediately after intervention, and 2 hours after intervention

Vocal performances will be audiovisually recorded and evaluated by blinded independent expert raters using an adapted analytical vocal-performance rubric based on Gynnild (2015). The rubric evaluates technique, language/text, musicality, ability to communicate, and choice of repertoire. Performance grades range from A to F and are converted to numerical values from 5 to 0, with higher scores indicating better vocal performance. Because all participants perform the same standardized repertoire, the choice-of-repertoire domain will not contribute to the primary performance score. The primary vocal-performance score will be calculated from the applicable rubric domains, and changes over time will be compared between the active and sham groups.

Baseline, immediately after intervention, and 2 hours after intervention

Toissijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Change in Self-Reported Vocal Performance
Aikaikkuna: Baseline, immediately after intervention, and 2 hours after intervention

Participants will rate their own vocal performance on a numerical rating scale from 0 to 10, where 0 represents the worst possible performance that day and 10 represents the best possible performance that day. Higher scores indicate better self-perceived vocal performance.

Baseline, immediately after intervention, and 2 hours after intervention
Change in Self-Reported Nervousness
Aikaikkuna: Baseline, immediately after intervention, and 2 hours after intervention

Participants will rate their nervousness related to the vocal performance on a numerical rating scale from 0 to 10, where 0 represents no nervousness and 10 represents the highest level of nervousness experienced. Higher scores indicate greater self-reported nervousness.

Baseline, immediately after intervention, and 2 hours after intervention
Change in Self-Reported Confidence
Aikaikkuna: Baseline, immediately after intervention, and 2 hours after intervention

Participants will rate their confidence regarding the vocal performance on a numerical rating scale from 0 to 10, where 0 represents no confidence and 10 represents the highest possible confidence. Higher scores indicate greater self-reported confidence.

Baseline, immediately after intervention, and 2 hours after intervention
Participant Perception of Intervention Allocation
Aikaikkuna: At the end of the study session, approximately 2 hours after intervention

Participants will report whether they believe they received active stimulation, sham stimulation, or whether they do not know which condition they received. Responses will be used to evaluate the effectiveness of participant blinding.

At the end of the study session, approximately 2 hours after intervention
Completion Rate
Aikaikkuna: From enrollment through completion of the 2-hour post-intervention assessment

Completion rate will be calculated as the proportion of enrolled participants who complete all planned study procedures, including baseline assessment, the assigned tDCS or sham session, immediate post-intervention assessment, and the 2-hour post-intervention assessment. The number and percentage of participants completing the full study protocol will be reported.

From enrollment through completion of the 2-hour post-intervention assessment
Protocol Adherence
Aikaikkuna: From enrollment through completion of the 2-hour post-intervention assessment.

Protocol adherence will be assessed as the proportion of enrolled participants who complete the assigned stimulation session and all planned study assessments according to the predefined protocol without major protocol deviations. The number and percentage of participants with complete adherence will be reported, and protocol deviations will be documented.

From enrollment through completion of the 2-hour post-intervention assessment.

Yhteistyökumppanit ja tutkijat

Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.

Sponsori

Yhteistyökumppanit

Julkaisuja ja hyödyllisiä linkkejä

Tutkimusta koskevien tietojen syöttämisestä vastaava henkilö toimittaa nämä julkaisut vapaaehtoisesti. Nämä voivat koskea mitä tahansa tutkimukseen liittyvää.

Yleiset julkaisut

Opintojen ennätyspäivät

Nämä päivämäärät seuraavat ClinicalTrials.gov-sivustolle lähetettyjen tutkimustietueiden ja yhteenvetojen edistymistä. National Library of Medicine (NLM) tarkistaa tutkimustiedot ja raportoidut tulokset varmistaakseen, että ne täyttävät tietyt laadunvalvontastandardit, ennen kuin ne julkaistaan ​​julkisella verkkosivustolla.

Opi tärkeimmät päivämäärät

Opiskelun aloitus (Arvioitu)

Keskiviikko 7. lokakuuta 2026

Ensisijainen valmistuminen (Arvioitu)

Keskiviikko 30. joulukuuta 2026

Opintojen valmistuminen (Arvioitu)

Torstai 31. joulukuuta 2026

Opintoihin ilmoittautumispäivät

Ensimmäinen lähetetty

Keskiviikko 30. syyskuuta 2026

Ensimmäinen toimitettu, joka täytti QC-kriteerit

Keskiviikko 30. syyskuuta 2026

Ensimmäinen Lähetetty (Todellinen)

Tiistai 6. lokakuuta 2026

Tutkimustietojen päivitykset

Viimeisin päivitys julkaistu (Todellinen)

Tiistai 13. lokakuuta 2026

Viimeisin lähetetty päivitys, joka täytti QC-kriteerit

Keskiviikko 7. lokakuuta 2026

Viimeksi vahvistettu

Torstai 1. lokakuuta 2026

Lisää tietoa

Tähän tutkimukseen liittyvät termit

Muut tutkimustunnusnumerot

  • 01375026.7.0000.5235-VOCAL

Yksittäisten osallistujien tietojen suunnitelma (IPD)

Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?

PÄÄTTÄMÄTÖN

Lääke- ja laitetiedot, tutkimusasiakirjat

Tutkii yhdysvaltalaista FDA sääntelemää lääkevalmistetta

Ei

Tutkii yhdysvaltalaista FDA sääntelemää laitetuotetta

Ei

Nämä tiedot haettiin suoraan verkkosivustolta clinicaltrials.gov ilman muutoksia. Jos sinulla on pyyntöjä muuttaa, poistaa tai päivittää tutkimustietojasi, ota yhteyttä register@clinicaltrials.gov. Heti kun muutos on otettu käyttöön osoitteessa clinicaltrials.gov, se päivitetään automaattisesti myös verkkosivustollemme .