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Female Teacher's Voice During Teaching

The Well-being of Female Teacher's Voice During Teaching

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03382535
Enrollment
54
Registered
2017-12-26
Start date
2009-12-07
Completion date
2016-06-14
Last updated
2017-12-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Functional Voice Disorder

Keywords

Voice disorder, Teacher's voice, Voice SPL (Voice sound pressure level), Voice F0 (Voice fundamental frequency), Voice therapy, Voice accumulator, Activity noise, Classroom

Brief summary

Two voice therapy methods are compared. Activity noise levels and vocal load of teachers during teaching in primary school classrooms are evaluated. Acoustic and Workshop Interventions are implemented in order to reduce noise level during lesson.

Detailed description

Due to the voice disorders, teachers are a major customer group for voice therapy. The main part of the study is comparison of two voice therapy methods. There are several factors in the classroom that increase teacher's risk of voice disorders. One of the most significant is high noise level during lessons. This study explores the noise conditions the teachers are working in and how these conditions are related to the voice parameters and symptoms. Finally, the study aims to determine whether classroom noise level can be lowered by improving classroom acoustics and by noise reducing workshops for teachers and pupils.

Interventions

BEHAVIORALVoice therapy

Voice therapy with direct and indirect therapy elements.

BEHAVIORALVoice therapy with carryover strategies

Voice therapy with direct and indirect therapy elements and supplementary tasks and reminders.

OTHERControl group

No therapy during eight weeks. After the control period half of the group will be provided with Voice therapy and half with Voice therapy with carryover strategies.

Sponsors

Tampere University
CollaboratorOTHER
Oulu University Hospital
CollaboratorOTHER
Umeå University
CollaboratorOTHER
Sonvox AB
CollaboratorUNKNOWN
University of Oulu
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Participants are not told what kind of a therapy they are receiving.

Intervention model description

Participants are randomly divided into three groups. Group 1: Voice therapy. Group 2: Voice therapy with carryover strategies (supplementary tasks and reminders). Group 3. Controls. No treatment during control period. After the control period participants are having Voice therapy or Voice therapy with carryover strategies.

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* Female teachers or teachers of special needs children from elementary schools * Voice symptoms and willingness to participate in voice therapy * Mother tongue Finnish * No hearing loss, no need to use a hearing aid * Non-smoking * No neurological diseases * No voice therapy during past year * Successful phoniatric examination with rigid laryngoscopy or nasal endoscopy

Exclusion criteria

* Mother tongue other than Finnish * Need to use a hearing aid * Need for medical treatment in the larynx * Abnormalities of the larynx * Vocal cord paresis * Laryngitis * Posterior hypertrophy

Design outcomes

Primary

MeasureTime frameDescription
The change of the well-being of the teachers' voice.Up to one week before the interventions, up to one week after the interventions, 6 months after the interventions, 1 year and 2 years after the interventions and up to one week after the control time (concerning control group).Subjective evaluation.Data collected with a questionnaire (Voice Activity and Participation Profile, VAPP) from the participants, answers given on a visual analogical scale (VAS) of 100 mm (0 = no disorder, 100 = extreme disorder).

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026