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

Voice Rest Versus Hypofunctional Whispering After Phonosurgery

maanantai 13. heinäkuuta 2026 päivittänyt: Celal Emre Çavlan

The Clinical Effects of Absolute Voice Rest and Hypofunctional Whispering After Phonosurgery

This randomized controlled trial compares two postoperative voice behavior protocols in patients undergoing microlaryngeal surgery (phonosurgery) for benign vocal fold lesions such as polyps, cysts, and Reinke's edema. After surgery, patients often need to rest their voice while the vocal folds heal. Traditionally, patients are advised to observe absolute voice rest (complete silence) for several days. However, complete silence can be difficult to maintain and may cause psychological and social burden.

The purpose of this study is to find out whether a five-day period of hypofunctional (soft, low-effort) whispering is as safe and effective as five days of absolute voice rest after phonosurgery. Patients were randomly assigned to one of two groups: absolute voice rest or hypofunctional whispering, for the first five days after surgery. From day six onward, both groups received the same standardized voice therapy delivered by a speech-language pathologist.

Patients were evaluated before surgery and again at one month and three months after surgery. The main measure was the change in the Voice Handicap Index-30 (VHI-30), a patient-reported questionnaire about the impact of voice problems on daily life. Additional measures included voice-related quality of life, acoustic voice analysis, aerodynamic measurements, perceptual voice ratings, and videolaryngostroboscopic examination of the vocal folds. The study also assessed protocol compliance, quality of life, and patient satisfaction during the five-day protocol period

Tutkimuksen yleiskatsaus

Yksityiskohtainen kuvaus

Background: Benign vocal fold lesions (polyps, cysts, and Reinke's edema) are among the most common organic causes of dysphonia and are frequently treated with microlaryngeal phonosurgery. The optimal postoperative voice behavior protocol remains debated. Absolute voice rest has traditionally been recommended to protect the healing vocal fold mucosa, but growing evidence suggests that its theoretical advantage may not translate into superior clinical outcomes, and complete silence imposes a considerable psychosocial burden. Studies directly comparing hypofunctional whispering with absolute voice rest using a prospective randomized design are limited.

Objective: To compare the effects of two postoperative voice behavior protocols applied for five days after phonosurgery for benign vocal fold lesions - absolute voice rest versus communication limited to hypofunctional whispering - on patient-reported voice outcomes, acoustic parameters, aerodynamic measurements, perceptual evaluation, and videolaryngostroboscopic findings.

Design: Prospective, single-center, randomized, parallel-group controlled trial conducted in the Department of Otorhinolaryngology - Head and Neck Surgery at Marmara University School of Medicine.

Participants: Patients with benign vocal fold lesions (polyp, cyst, or Reinke's edema) scheduled for microlaryngeal surgery who met the inclusion criteria. Sixteen patients were enrolled and analyzed.

Randomization and Blinding: Patients were allocated 1:1 into two groups using computer-based random number generation, performed after preoperative assessment and immediately before surgery. Due to the nature of the intervention, blinding of patients and the surgical team was not possible. However, perceptual (CAPE-V) recordings were rated by two independent speech-language pathologists, and videolaryngostroboscopic recordings by two independent laryngologists, all blinded to group assignment.

Interventions: All patients underwent suspension microlaryngoscopy under general anesthesia by a single surgeon, using a microflap technique with preservation of the superficial layer of the lamina propria. Group 1 observed absolute voice rest for five postoperative days; Group 2 followed a hypofunctional whispering protocol (soft, low-effort whispering) for five postoperative days. From postoperative day six onward, both groups received the same standardized voice therapy protocol delivered by an experienced speech-language pathologist.

Outcome Measures: The primary outcome was the change in Voice Handicap Index-30 (VHI-30) total score from baseline to postoperative month 3, with the established minimal clinically important difference (MCID) of 18 points used as a reference. Secondary outcomes included Voice-Related Quality of Life (V-RQOL), Acoustic Voice Quality Index (AVQI) and traditional acoustic parameters (F0, jitter, shimmer, HNR), aerodynamic measurements (maximum phonation time and s/z ratio), perceptual evaluation according to the CAPE-V protocol, and videolaryngostroboscopic findings scored with the VALI protocol. All assessments were performed at three time points: preoperatively, postoperative month 1, and postoperative month 3. At the end of the five-day protocol period, patients completed a structured questionnaire assessing protocol compliance, quality of life, and satisfaction.

Statistical Analysis: Between-group and within-time comparisons were performed using linear mixed model analysis, with time, group, and time-by-group interaction as fixed effects and patient as a random effect. The difference between the two protocols was assessed via the significance of the time-by-group interaction term. Questionnaire comparisons were analyzed using Mann-Whitney U and Fisher exact tests. The proportion of patients exceeding the VHI-30 MCID threshold was compared using the chi-square test.

Opintotyyppi

Interventio

Ilmoittautuminen (Todellinen)

16

Vaihe

  • Ei sovellettavissa

Yhteystiedot ja paikat

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

Opiskelupaikat

    • Istanbul
      • Istanbul, Istanbul, Turkki (Türkiye), 34854
        • Marmara University School of Medicine, Department of Otorhinolaryngology - Head and Neck Surgery

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

  • Aikuinen
  • Vanhempi Aikuinen

Hyväksyy terveitä vapaaehtoisia

Ei

Kuvaus

Inclusion Criteria:

  • Age 18 years or older
  • Diagnosis of a benign vocal fold lesion (vocal fold polyp, cyst, or Reinke's edema)
  • Scheduled for microlaryngeal (phonosurgery) surgery under general anesthesia
  • Able to complete voice assessments and comply with the assigned postoperative voice behavior protocol
  • Provided written informed consent

Exclusion Criteria:

  • Malignant or premalignant vocal fold lesions
  • Previous laryngeal surgery or radiotherapy to the head and neck
  • Neurological voice disorders (e.g., vocal fold paralysis, spasmodic dysphonia)
  • Significant psychiatric or cognitive impairment preventing protocol compliance
  • Active smoking without cessation in Reinke's edema cases where required (if applicable)
  • Inability or unwillingness to attend follow-up assessments

Opintosuunnitelma

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

Miten tutkimus on suunniteltu?

Suunnittelun yksityiskohdat

  • Ensisijainen käyttötarkoitus: Hoito
  • Jako: Satunnaistettu
  • Inventiomalli: Rinnakkaistehtävä
  • Naamiointi: Yksittäinen

Aseet ja interventiot

Osallistujaryhmä / Arm
Interventio / Hoito
Active Comparator: Absolute Voice Rest
Patients observed absolute voice rest (complete silence) for the first five postoperative days. From postoperative day six, they received a standardized voice therapy protocol delivered by a speech-language pathologist.
Complete voice rest (total silence) for five days after phonosurgery, followed by standardized voice therapy from day six.
Kokeellinen: Hypofunctional Whispering
Patients used a hypofunctional whispering protocol (soft, low-effort whispering) for the first five postoperative days. From postoperative day six, they received the same standardized voice therapy protocol delivered by a speech-language pathologist.
Soft, low-effort (hypofunctional) whispering for five days after phonosurgery, followed by standardized voice therapy from day six.

Mitä tutkimuksessa mitataan?

Ensisijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Change in Voice Handicap Index-30 (VHI-30) total score
Aikaikkuna: Baseline (preoperative), postoperative month 1, and postoperative month 3
The Voice Handicap Index-30 (VHI-30) is a 30-item patient-reported questionnaire assessing the physical, functional, and emotional impact of voice disorders. Total score ranges from 0 to 120, with higher scores indicating greater voice-related handicap. The primary outcome was the change in VHI-30 total score from baseline to postoperative month 3. The established minimal clinically important difference (MCID) of 18 points was used as a reference.
Baseline (preoperative), postoperative month 1, and postoperative month 3

Toissijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Change in Acoustic Voice Quality Index (AVQI)
Aikaikkuna: Baseline (preoperative), postoperative month 1, and postoperative month 3
The Acoustic Voice Quality Index (AVQI) is a multiparametric acoustic measure combining several acoustic parameters into a single score reflecting overall voice quality; higher values indicate more severe dysphonia. Calculated using Praat software.
Baseline (preoperative), postoperative month 1, and postoperative month 3
Change in Acoustic Voice Quality Index (AVQI)
Aikaikkuna: Baseline (preoperative), postoperative month 1, and postoperative month 3
Baseline (preoperative), postoperative month 1, and postoperative month 3
Change in Maximum Phonation Time (MPT)
Aikaikkuna: Baseline (preoperative), postoperative month 1, and postoperative month 3
Baseline (preoperative), postoperative month 1, and postoperative month 3
Change in s/z ratio
Aikaikkuna: Baseline (preoperative), postoperative month 1, and postoperative month 3
Baseline (preoperative), postoperative month 1, and postoperative month 3
Change in Auditory-Perceptual Voice Quality Assessed by the CAPE-V Protocol
Aikaikkuna: Baseline (preoperative), postoperative month 1, and postoperative month 3
Baseline (preoperative), postoperative month 1, and postoperative month 3
Change in Videolaryngostroboscopic Findings Assessed by the VALI Protocol
Aikaikkuna: Baseline (preoperative), postoperative month 1, and postoperative month 3
Baseline (preoperative), postoperative month 1, and postoperative month 3
Protocol Compliance Assessed by Visual Analog Scale (VAS)
Aikaikkuna: End of the five-day postoperative protocol period (postoperative day 5)
Self-reported protocol compliance measured with a study-specific (non-validated) structured questionnaire. Scores range from 0 to 100; higher scores indicate better compliance.
End of the five-day postoperative protocol period (postoperative day 5)
Quality of Life Impact Assessed by Visual Analog Scale (VAS)
Aikaikkuna: End of the five-day postoperative protocol period (postoperative day 5)
Impact on quality of life measured with a study-specific (non-validated) structured questionnaire covering general wellbeing, family communication, social life, occupational life, and psychological impact. Scores range from 0 to 100; higher scores indicate greater (worse) impact.
End of the five-day postoperative protocol period (postoperative day 5)
Patient Satisfaction Assessed by Visual Analog Scale (VAS)
Aikaikkuna: End of the five-day postoperative protocol period (postoperative day 5)
Patient satisfaction with the assigned voice behavior protocol measured with a study-specific (non-validated) structured questionnaire. Scores range from 0 to 100; higher scores indicate greater satisfaction.
End of the five-day postoperative protocol period (postoperative day 5)

Yhteistyökumppanit ja tutkijat

Täältä löydät tähän tutkimukseen osallistuvat ihmiset ja organisaatiot.

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 (Todellinen)

Torstai 20. helmikuuta 2025

Ensisijainen valmistuminen (Todellinen)

Keskiviikko 15. huhtikuuta 2026

Opintojen valmistuminen (Todellinen)

Lauantai 2. toukokuuta 2026

Opintoihin ilmoittautumispäivät

Ensimmäinen lähetetty

Keskiviikko 8. heinäkuuta 2026

Ensimmäinen toimitettu, joka täytti QC-kriteerit

Maanantai 13. heinäkuuta 2026

Ensimmäinen Lähetetty (Todellinen)

Keskiviikko 15. heinäkuuta 2026

Tutkimustietojen päivitykset

Viimeisin päivitys julkaistu (Todellinen)

Keskiviikko 15. heinäkuuta 2026

Viimeisin lähetetty päivitys, joka täytti QC-kriteerit

Maanantai 13. heinäkuuta 2026

Viimeksi vahvistettu

Keskiviikko 1. heinäkuuta 2026

Lisää tietoa

Tähän tutkimukseen liittyvät termit

Yksittäisten osallistujien tietojen suunnitelma (IPD)

Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?

EI

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 .

Tilaa