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Investigation of the Effectiveness of Group Voice Therapy in Children

NCT06124053 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 18

Last updated 2023-11-21

No results posted yet for this study

Summary

This study aims to investigate whether there is a difference between groups receiving "group voice therapy" and "individual voice therapy" in pediatric populations diagnosed with dysphonia. In this context, the goal is to comprehensively examine the effectiveness of "group voice therapy" in pediatric populations compared to similar studies in the literature. In line with this objective, it is aimed to comprehensively test its effectiveness by including perceptual and acoustic evaluation findings, objective and subjective assessments, and incorporating comparison and control groups into the study, as compared to similar studies in the literature.

Conditions

  • Dysphonia

Interventions

BEHAVIORAL

Group Voice Therapy

The "group voice therapy" intervention consists of a total of eight sessions. The session contents include both direct and indirect voice therapy approaches. Each group is composed of three participants. The session durations are planned to be 45-60 minutes each.

BEHAVIORAL

Individual Voice Therapy

The "individual voice therapy" intervention consists of a total of eight sessions. The session contents include both direct and indirect voice therapy approaches. The session durations are planned to be 45-60 minutes each.

BEHAVIORAL

Vocal Hygiene Education

Regarding vocal hygiene training, information related to voice production and respiratory characteristics will be provided, and guidance on correct and incorrect voice use will be given.

Sponsors & Collaborators

  • Hacettepe University

    lead OTHER

Principal Investigators

  • Fatma ESEN AYDINLI, Assoc. Prof. · Hacettepe University, Speech and Language Therapy Departmant

  • Meltem Çiğdem KİRAZLI, Ph.D. · Hacettepe University, Speech and Language Therapy Departmant

  • Taner Yılmaz, Prof. · Hacettepe University, Department of Otorhinolaryngology

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
7 Years
Max Age
11 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-11-15
Primary Completion
2024-11-30
Completion
2025-06-30

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06124053 on ClinicalTrials.gov