Female Teacher's Voice During Teaching

Sponsor
University of Oulu (Other)
Overall Status
Completed
CT.gov ID
NCT03382535
Collaborator
Tampere University (Other), Oulu University Hospital (Other), Umeå University (Other), Sonvox AB (Other)
54
3
78.2

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Voice therapy
  • Behavioral: Voice therapy with carryover strategies
  • Other: Control group
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
54 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
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.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.
Masking:
Single (Participant)
Masking Description:
Participants are not told what kind of a therapy they are receiving.
Primary Purpose:
Treatment
Official Title:
The Well-being of Female Teacher's Voice During Teaching
Actual Study Start Date :
Dec 7, 2009
Actual Primary Completion Date :
Dec 20, 2014
Actual Study Completion Date :
Jun 14, 2016

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Voice therapy

An individually tailored voice therapy where the order and length of voice treatment methods will depend on the nature of each subject's voice problems. The intervention will take eight weeks and average of eight sessions (a' 45 min).

Behavioral: Voice therapy
Voice therapy with direct and indirect therapy elements.

Experimental: Voice therapy with carryover strategies

A voice therapy as described above and an enhanced carryover program. By carryover we mean the process of extending new vocal skills outside the clinic. It includes supplementary tasks and reminders that will be tailored individually out of those direct and indirect methods that the subjects have adopted during therapy sessions. Additionally, the teachers will be doing vocal warm-up and relaxation exercises together with their pupils int the beginning and in the middle of a school day. The intervention will take eight weeks.

Behavioral: Voice therapy with carryover strategies
Voice therapy with direct and indirect therapy elements and supplementary tasks and reminders.

Other: Control group

No intervention during eight weeks since this group will act as a temporary control group. After eight weeks, half of the participants in this group will be provided with Voice therapy and half with Voice therapy with carryover strategies.

Other: Control 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.

Outcome Measures

Primary Outcome Measures

  1. 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).

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
Female
Accepts 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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Oulu
  • Tampere University
  • Oulu University Hospital
  • Umeå University
  • Sonvox AB

Investigators

  • Study Chair: Sirpa M Pirilä, MA, Ooulu

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Oulu
ClinicalTrials.gov Identifier:
NCT03382535
Other Study ID Numbers:
  • Ooulu
First Posted:
Dec 26, 2017
Last Update Posted:
Dec 26, 2017
Last Verified:
Dec 1, 2017
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Oulu
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 26, 2017