DeafnessNCT04241302
Development of a Mobile App FFVT vs FFCT : A RCT
A study testing Pure Tone Audiogram in people with Deafness, run by Ministry of Health, Malaysia at 1 site in Malaysia.
Trial summary
This is an open-labelled randomised controlled trial involving 2 groups which are Free Field voice test vs Free Field Click tests using digital hand-held devices. This study will be done at a sound-proof room in ORL clinic in Hospital Sultanah Aminah, Johor, Malaysia from January till July 2020. Read more about this study
- Who is it for?
- Ages 18 to 80 years
- Conditions the study is for
- Deafness
- What is being tested?
- Pure Tone Audiogram
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 50 participants
- Where
- 1 siteMalaysia
- Study dates
- 1 Jan 2020to 1 Jul 2020
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 80 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age 18-80 years old ii) Chief complaint of reduced hearing -unilaterally or bilaterally iii) Able to communicate with the examiners iv) Post-traumatic patients with uni/bilateral hearing loss
Who cannot join
- Age < 18 or > 80 years old ii) Uncooperative patient iii) Not consented iv) Intellectually-challenged v) Pregnant ladies vi) Previous ear surgery/ear tumor
Trial locations and contacts
1 site in 1 country.
Malaysia1 site
Hospital Sultanah Aminah Johor Bahru
Johor Bahru, Johor, 80000
About this study
Official title: Development of a Mobile-app Based Free Field Click Test Against Conventional Free Field Voice Test
This is an open-labelled randomised controlled trial involving 2 groups which are Free Field voice test vs Free Field Click tests using digital hand-held devices. This study will be done at a sound-proof room in ORL clinic in Hospital Sultanah Aminah, Johor, Malaysia from January till July 2020.
Read the detailed description
This is an open-labelled randomized controlled trial involving 2 groups which are Free Field voice test vs Free Field Click test (digital hand-held device). There will be no follow up for these participants as it is a one off assessment in most cases. Participants from the Otolaryngology clinic of Hospital Sultanah Aminah Johor Bahru will initially be screened during office hours for suitability based on our inclusion and exclusion criteria. Participants whom are interested will then be counselled and a consent form will be provided to the participants and he/she will be given sufficient time to consider before providing a signature on the consent forms.
The app is designed by the investigators using a broadband (500-3000 Hz) click sound of 30-40 dB for soft sound/whisper and 60-70dB for loud sound/conversation voice. This app is designed by using the Flutter-Dart programming tool and the speaker is produced via hand-held devices of Apple and Android brands. The tone is produced 3 times, with 2 out of 3 answers are considered as the participant's hearing threshold. The investigators stands at the distance of 2 feet away behind the seated participant and a soft sound from the FFCT is tested. The participant is then asked to respond yes or to nod if able to hear the sound. When the participant is unable to answer or no response is received upon third testing, the examiner then moves closer to 6 inches to the participant and again the soft sound is tested thrice. Loud sound is then tested if the participant is unable to respond, starting from 2 feet distance for three times. And then, the loud sound is tested at 6 inches of distance if no further response is obtained.
The same is done for the group of participants randomised into the Free Field voice test group. The investigator will inform the participant to repeat a sequence of Spondees words or a combination of numbers and letters whispered by the examiner initially. The investigator will be standing at the same distances as in the Free Field Click test examination (starting with 2 feet). If the participant fails to hear the whispered voice at 2 feet, the investigator increases the loudness of voice to conversational tone at the same distance. The test is repeated thrice each time with a different set of Spondee words to avoid the participants from recognizing the same sequence. If the participant is unable to respond, the investigator moves closer to 6 inches and whispers to the participant, and if no further response, then, conversational voice is used. The participant's free-field threshold is the voice and distance level at which more than 50% correct is obtained.
Both the FFVT and FFCT tests are done in a sound-proof room or a reasonably quiet room. The investigator stands behind the participant throughout the examination to prevent any lip reading. Each ear is tested individually, starting with the better ear and the non-test ear is masked by the participant by either gently occluding the ear canal with a finger or by tragal rubbing. The other ear is assessed similarly. Expected duration for the completion of a FFVT or FFCT is estimated to be approximately 5-10 minutes depending on severity of hearing loss where-else the duration for a diagnostic PTA would take between 10-20 minutes depending on complexity of hearing loss. This is a standard procedure in PTA practice and no additional steps were undertaken specifically for the purpose of this study.
As this is a study to compare the sensitivity and specificity of FFVT and FFCT, the study end-point involves the subjective hearing threshold obtained from the participant upon hearing the tested sound. The subjective threshold is measured under 5 categories which is whispering sounds at 2 feet (from the participants), whispering sounds at 6 inches, Conversational sounds at 2 feet, Conversational sounds at 6 inches and finally not being able to hear at all. The measurements of the 2 groups will then be compared to the pure tone average obtained through pure tone audiogram.
- Conditions
- Deafness
- Being tested
- Pure Tone Audiogram
- Keywords
- Mobile App, Clinical trial, Audiology, Deafness
- Medical subject headings
- Deafness
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Pure Tone AudiogramDiagnostic test
A Pure Tone Audiogram is done in a sound proof room in both cases of Free Field Voice Test and Free Field Click Tests to identify the Pure Tone Average (Hearing Threshold Average of 500Hz,1000Hz and 2000Hz).
| Study group | Role | What they receive |
|---|---|---|
| Free Field Voice test | Active comparator | The examiner will inform the patient to repeat a sequence of Spondee words or a combination of numbers and letters whispered by the examiner initially. The examiner will be standing at the same distances as in the FFCT examination (starting with 2 feet). If the patient fails to hear the whispered voice at 2 feet, the examiner increases the loudness of voice to conversational tone at the same distance. The test is repeated thrice each time with a different set of Spondee words to avoid the patients recognizing the same sequence. If the patient is unable to respond, the examiner moves closer to 6 inches and whispers to the patient, and if no further response, then, conversational voice is used. The patient's free-field threshold is the voice and distance level at which more than 50% correct is obtained. Receives: Diagnostic Test: Pure Tone Audiogram |
| Free Field Click Test | Experimental | The app is designed by our team by a broadband (500-3000 Hz) click sound of 30-40 dB for soft sound/whisper and 60-70dB for loud sound/conversation voice. This app is designed by the Flutter-Dart programming tool and the speaker is produced via hand-held devices of Apple and Android brands. The tone is produced 3 times, with 2 out of 3 answers are considered as the patient's hearing threshold. The examiner stands at the distance of 2 feet away behind the seated patient and a soft sound from the FFCT is tested. The patient is then asked to respond yes or to nod if able to hear the sound. When the patient is unable to answer or no response is received upon thrice testing, the examiner then moves closer to 6 inches to the patient and again the soft sound is tested thrice. Loud sound is then tested if the patient is unable to respond, starting from 2 feet distance for three times. And then, the loud sound is tested at 6 inches of distance if no further response is obtained. Receives: Diagnostic Test: Pure Tone Audiogram |
What is being measured
The primary outcome is the main question the study is designed to answer.
Subjective hearing threshold
To compare the sensitivity and specificity of FFVT and FFCT, the study end-point involves the subjective hearing threshold obtained from the patient upon hearing the tested sound and comparing results to Pure Tone Audiogram and obtaining the Pure Tone Average
Measured: 15 minutes
Secondary outcomes (4)
Gender comparison
Comparison of sensitivity of hearing threshold detection of both Free field Voice test and Free Field click test between genders
Measured: 15 minutes
Age Comparison
Comparison of sensitivity of hearing threshold detection of both Free field Voice test and Free Field click test on different age groups
Measured: 15 minutes
Tympanogram comparison
Comparison of sensitivity of hearing threshold detection of both Free field Voice test and Free Field click test when tested with a tympanogram device
Measured: 15 minutes
Laterality comparison
Comparison of sensitivity of hearing threshold detection of both Free field Voice test and Free Field click test between unilateral and bilateral hearing loss
Measured: 15 minutes
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Jan 2020
- Study start1 Jan 2020
- Primary completion1 Jul 2020
- Study completion1 Jul 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (3)Papers the sponsor has linked to this study.
- Other trials for DeafnessStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Diagnosis
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Free Field Voice test vs Free Field Click Test
- Masking
- None (open label)
- Enrolment
- 50 participants (actual)
Sponsor and investigators
- Lead sponsor
- Ministry of Health, Malaysia
- Sponsor type
- Other government
- Responsible party
- Principal investigator, Goh Liang Chye, Ministry of Health, Malaysia
- Investigators
- Goh Liang Chye, MS (ORL-HNS), Study director, OtorhinolaryngologistThilaga Rajendren, MBBS, Principal investigator, Medical officer
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04241302
- Sponsor's protocol ID
- 52296
- Status last verified
- Aug 2020
- First submitted
- 22 Jan 2020
- Last updated
- 1 Sep 2020
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: There is not a plan to make IPD available.
Publications
Pirozzo S, Papinczak T, Glasziou P. Whispered voice test for screening for hearing impairment in adults and children: systematic review. BMJ. 2003 Oct 25;327(7421):967. doi: 10.1136/bmj.327.7421.967.
PubMed 14576249Dempster JH, Mackenzie K. Clinical role of free-field voice tests in children. Clin Otolaryngol Allied Sci. 1992 Feb;17(1):54-6. doi: 10.1111/j.1365-2273.1992.tb00988.x.
PubMed 1555319McShefferty D, Whitmer WM, Swan IR, Akeroyd MA. The effect of experience on the sensitivity and specificity of the whispered voice test: a diagnostic accuracy study. BMJ Open. 2013 Apr 18;3(4):e002394. doi: 10.1136/bmjopen-2012-002394. Print 2013.
PubMed 23604349
Study at a glance
From the registry record, last updated by the sponsor on 1 Sep 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Development of a Mobile-app Based Free Field Click Test Against Conventional Free Field Voice Test
- ClinicalTrials.gov ID
- NCT04241302
- Acronym / sponsor ID
- 52296
- Conditions
- Deafness
- Keywords
- Mobile App, Clinical trial, Audiology, Deafness
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 50 participants (actual)
- Lead sponsor
- Ministry of Health, MalaysiaOther government
- Study start
- 1 Jan 2020 (actual)
- Primary completion
- 1 Jul 2020 (actual)
- Study completion
- 1 Jul 2020 (actual)
- First posted
- 27 Jan 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is an open-labelled randomised controlled trial involving 2 groups which are Free Field voice test vs Free Field Click tests using digital hand-held devices. This study will be done at a sound-proof room in ORL clinic in Hospital Sultanah Aminah, Johor, Malaysia from January till July 2020.
Detailed description
This is an open-labelled randomized controlled trial involving 2 groups which are Free Field voice test vs Free Field Click test (digital hand-held device). There will be no follow up for these participants as it is a one off assessment in most cases. Participants from the Otolaryngology clinic of Hospital Sultanah Aminah Johor Bahru will initially be screened during office hours for suitability based on our inclusion and exclusion criteria. Participants whom are interested will then be counselled and a consent form will be provided to the participants and he/she will be given sufficient time to consider before providing a signature on the consent forms.
The app is designed by the investigators using a broadband (500-3000 Hz) click sound of 30-40 dB for soft sound/whisper and 60-70dB for loud sound/conversation voice. This app is designed by using the Flutter-Dart programming tool and the speaker is produced via hand-held devices of Apple and Android brands. The tone is produced 3 times, with 2 out of 3 answers are considered as the participant's hearing threshold. The investigators stands at the distance of 2 feet away behind the seated participant and a soft sound from the FFCT is tested. The participant is then asked to respond yes or to nod if able to hear the sound. When the participant is unable to answer or no response is received upon third testing, the examiner then moves closer to 6 inches to the participant and again the soft sound is tested thrice. Loud sound is then tested if the participant is unable to respond, starting from 2 feet distance for three times. And then, the loud sound is tested at 6 inches of distance if no further response is obtained.
The same is done for the group of participants randomised into the Free Field voice test group. The investigator will inform the participant to repeat a sequence of Spondees words or a combination of numbers and letters whispered by the examiner initially. The investigator will be standing at the same distances as in the Free Field Click test examination (starting with 2 feet). If the participant fails to hear the whispered voice at 2 feet, the investigator increases the loudness of voice to conversational tone at the same distance. The test is repeated thrice each time with a different set of Spondee words to avoid the participants from recognizing the same sequence. If the participant is unable to respond, the investigator moves closer to 6 inches and whispers to the participant, and if no further response, then, conversational voice is used. The participant's free-field threshold is the voice and distance level at which more than 50% correct is obtained.
Both the FFVT and FFCT tests are done in a sound-proof room or a reasonably quiet room. The investigator stands behind the participant throughout the examination to prevent any lip reading. Each ear is tested individually, starting with the better ear and the non-test ear is masked by the participant by either gently occluding the ear canal with a finger or by tragal rubbing. The other ear is assessed similarly. Expected duration for the completion of a FFVT or FFCT is estimated to be approximately 5-10 minutes depending on severity of hearing loss where-else the duration for a diagnostic PTA would take between 10-20 minutes depending on complexity of hearing loss. This is a standard procedure in PTA practice and no additional steps were undertaken specifically for the purpose of this study.
As this is a study to compare the sensitivity and specificity of FFVT and FFCT, the study end-point involves the subjective hearing threshold obtained from the participant upon hearing the tested sound. The subjective threshold is measured under 5 categories which is whispering sounds at 2 feet (from the participants), whispering sounds at 6 inches, Conversational sounds at 2 feet, Conversational sounds at 6 inches and finally not being able to hear at all. The measurements of the 2 groups will then be compared to the pure tone average obtained through pure tone audiogram.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Free Field Voice test vs Free Field Click Test
| Arm | Type | Receives |
|---|---|---|
| Free Field Voice test | Active comparator | Diagnostic Test: Pure Tone AudiogramThe examiner will inform the patient to repeat a sequence of Spondee words or a combination of numbers and letters whispered by the examiner initially. The examiner will be standing at the same distances as in the FFCT examination (starting with 2 feet). If the patient fails to hear the whispered voice at 2 feet, the examiner increases the loudness of voice to conversational tone at the same distance. The test is repeated thrice each time with a different set of Spondee words to avoid the patients recognizing the same sequence. If the patient is unable to respond, the examiner moves closer to 6 inches and whispers to the patient, and if no further response, then, conversational voice is used. The patient's free-field threshold is the voice and distance level at which more than 50% correct is obtained. |
| Free Field Click Test | Experimental | Diagnostic Test: Pure Tone AudiogramThe app is designed by our team by a broadband (500-3000 Hz) click sound of 30-40 dB for soft sound/whisper and 60-70dB for loud sound/conversation voice. This app is designed by the Flutter-Dart programming tool and the speaker is produced via hand-held devices of Apple and Android brands. The tone is produced 3 times, with 2 out of 3 answers are considered as the patient's hearing threshold. The examiner stands at the distance of 2 feet away behind the seated patient and a soft sound from the FFCT is tested. The patient is then asked to respond yes or to nod if able to hear the sound. When the patient is unable to answer or no response is received upon thrice testing, the examiner then moves closer to 6 inches to the patient and again the soft sound is tested thrice. Loud sound is then tested if the patient is unable to respond, starting from 2 feet distance for three times. And then, the loud sound is tested at 6 inches of distance if no further response is obtained. |
Who may qualify
- Ages
- 18 to 80 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- Age 18-80 years old ii) Chief complaint of reduced hearing -unilaterally or bilaterally iii) Able to communicate with the examiners iv) Post-traumatic patients with uni/bilateral hearing loss
Key exclusion criteria (1 listed)
- Age < 18 or > 80 years old ii) Uncooperative patient iii) Not consented iv) Intellectually-challenged v) Pregnant ladies vi) Previous ear surgery/ear tumor
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Pure Tone AudiogramA Pure Tone Audiogram is done in a sound proof room in both cases of Free Field Voice Test and Free Field Click Tests to identify the Pure Tone Average (Hearing Threshold Average of 500Hz,1000Hz and 2000Hz). | Diagnostic test | Free Field Click Test, Free Field Voice test |
Primary outcome
Subjective hearing threshold
Time frame: 15 minutes
To compare the sensitivity and specificity of FFVT and FFCT, the study end-point involves the subjective hearing threshold obtained from the patient upon hearing the tested sound and comparing results to Pure Tone Audiogram and obtaining the Pure Tone Average
4 secondary outcomes
Gender comparison
Time frame: 15 minutes
Age Comparison
Time frame: 15 minutes
Tympanogram comparison
Time frame: 15 minutes
Laterality comparison
Time frame: 15 minutes
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Sep 2020.
- Results publication: PubMed 14576249Pirozzo S, Papinczak T, Glasziou P. Whispered voice test for screening for hearing impairment in adults and children: systematic review. BMJ. 2003 Oct 25;327(7421):967. doi: 10.1136/bmj.327.7421.967.
- Results publication: PubMed 1555319Dempster JH, Mackenzie K. Clinical role of free-field voice tests in children. Clin Otolaryngol Allied Sci. 1992 Feb;17(1):54-6. doi: 10.1111/j.1365-2273.1992.tb00988.x.
- Results publication: PubMed 23604349McShefferty D, Whitmer WM, Swan IR, Akeroyd MA. The effect of experience on the sensitivity and specificity of the whispered voice test: a diagnostic accuracy study. BMJ Open. 2013 Apr 18;3(4):e002394. doi: 10.1136/bmjopen-2012-002394. Print 2013.
- Individual participant dataSharing planned: No. There is not a plan to make IPD available.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Goh Liang Chye, MS (ORL-HNS) study director
Otorhinolaryngologist
Thilaga Rajendren, MBBS principal investigator
Medical officer
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Pure Tone Audiogram in people with Deafness, run by Ministry of Health, Malaysia at 1 site in Malaysia.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 1 Sep 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Malaysia. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Subjective hearing threshold (time frame: 15 minutes). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04241302, which also lists 3 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Sep 2020.