Hearing LossPLUS-OptimalNCT07506408
Randomised Study of Web-Based Auditory Training With Varying Perceptual and Cognitive Demands on Training Gains and Generalised Speech, Cognitive, and Communication Outcomes
A study testing Practice Listening and Understand Speech (PLUS) in people with Hearing Loss, run by University of Nottingham at 1 site in United Kingdom.
Trial summary
WP1: PLUS-Auditory Training The goal of this experimental study is to better understand how task difficulty affects on-task learning thresholds and generalised benefits in two PLUS auditory training tasks involving perceptual and cognitive learning in adults aged 18+ (no upper age limit) with listening difficulties. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Hearing Loss
- What is being tested?
- Practice Listening and Understand Speech (PLUS)
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 120 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- 13 Mar 2026to 1 Feb 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Adults (aged 18+ years, no upper age limit);
- Poorer performance on the DTT (SRT of -5.5 dB SNR or higher, as defined by Dawes, 2013) completed without hearing aid(s) for those who typically use them;
- Non-hearing device users or hearing aid(s) owner;
- Ability to read and understand English;
- Ability to provide informed consent;
- Access to the internet;
- Access to functional built-in speakers, external speakers, or headphones.
Who cannot join
- Failure to meet inclusion criteria;
- Having previous auditory training experience;
- Cochlear implant users.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United Kingdom1 site, 1 recruiting
- Recruiting
NIHR Nottingham Biomedical Research Centre
Nottingham, Nottinghamshire, NG1 5DU
Natalie Lerigo-Smith, MSc, +44 (0)115 8232600, natalie.lerigo-smith1@nottingham.ac.uk
Helen Henshaw, PhD, +44 (0) 115 8232606, helen.henshaw@nottingham.ac.uk
About this study
Official title: PLUS-Optimal for Adults With Listening Difficulties: Investigating the Roles of Listening and Thinking Skills in Online Training Across Different Groups
WP1: PLUS-Auditory Training
The goal of this experimental study is to better understand how task difficulty affects on-task learning thresholds and generalised benefits in two PLUS auditory training tasks involving perceptual and cognitive learning in adults aged 18+ (no upper age limit) with listening difficulties. The main question it aims to answer is:
Read more
- Does adjusting task difficulty in PLUS, by manipulating the perceptual and cognitive demands of the phonemic discrimination and competing speech tasks, affect on-task learning thresholds and off-task performance in adults with listening difficulties?
Researchers will compare the two experimental arms (easy/hard) to see whether adjusting task difficulty influences on-task learning thresholds and off-task performance.
Participants will:
- Be randomly assigned to one of two training programs (phonemic discrimination or competing speech) within the two experimental arms (easy/hard);
- Perform training for a minimum of 30 minutes per day, 5 days per week, for two weeks (total 10 training sessions, 5 hours of training);
- Complete pre- and post- training assessments to measure on-task learning performance and change in performance for untrained measures of speech perception, cognition and self-reported outcomes.
WP2: Post-Training Focus Groups
The goal of this observational study is to gain in-depth qualitative insights into participants' motivations, experiences of task difficulty, and perceived benefits across the PLUS-AT training groups in adults aged 18+ (no upper age limit) with listening difficulties. The main question it aims to answer is:
- How do participants describe their experiences and perceptions of PLUS-AT, particularly regarding task difficulty and self-perceived changes in listening, hearing, thinking, and quality of life?
Researchers will explore participant experiences across the two experimental arms (easy/hard) to determine whether motivations for seeking auditory training, knowledge and beliefs about auditory training, attitudes toward PLUS-AT difficulty, and self-perceived changes in listening, hearing, thinking, and quality of life differ.
A subset of participants (n = 20) will:
- Be invited from WP1 to join one of four online focus groups (60-90 minutes via Microsoft Teams);
- Attend the focus group corresponding to their assigned training program (phonemic discrimination or competing-speech) within the two experimental arms (easy/hard);
- Share their experiences of completing PLUS-AT.
Read the detailed description
Hearing loss (HL) is a progressive, long-term condition without cure, affecting 18 million people in the UK, which is approximately one in three adults. Globally, HL is the third leading cause of years lived with disability and has major individual, societal, and economic consequences. When unmanaged, HL can lead to communication difficulties, social withdrawal, depression, reduced quality of life, accelerated cognitive decline, and increased dementia risk.
A key challenge reported by people with HL is the difficulty hearing speech in noisy environments, which often persists even when hearing aids (HAs) are used. HAs are the primary management option for HL, but uptake and consistent use is low. Of the 6.7 million people in the UK who could benefit from them, many people do not seek help for their hearing difficulties, and only around 2 million have hearing aids, with non-use estimated to range from 3 to 24%. Therefore, it is essential to develop interventions that can work either as a precursor to or adjacent with HAs to effectively address listening and hearing difficulties.
Auditory training (AT) delivered via internet-accessible devices such as phones or laptops, can be used before or alongside hearing devices such as HAs. As a low-cost intervention, AT supports the self-management of HL and listening difficulties and can be tailored to individual needs. Training itself involves focused listening exercises designed to improve everyday listening, especially in noise. Research shows that AT can improve speech perception throughout an adult's lifespan. It can help individuals improve their ability to distinguish speech in challenging environments like restaurants or family gatherings.
PLUS is a web-based app, standing for Practice Listening and Understanding Speech, developed at the University of Nottingham as an auditory-cognitive training programme. It builds on a decade of research indicating that domain-general improvements in cognitive processing, rather than auditory processing alone, drive the transfer of learning (generalised benefits) to untrained stimuli or tasks. Designed as a cognitively demanding speech training programme, PLUS aims to maximise the transfer of learning to real-world benefits for people with hearing loss. The auditory-cognitive approach was adopted since speech-based tasks are essential for maintaining user motivation and ensuring the training is perceived as relevant to hearing. PLUS has many different settings which changes the task difficulty and influences the level of perceptual and cognitive demand on the learner. It is not known which settings are the most optimal for maximal on-task learning and transfer of learning to everyday listening. The study outlined in this protocol seeks to understand how task difficulty in PLUS affects on-task learning thresholds and generalised benefits in populations with listening difficulties as a first step towards creating an optimal AT intervention for people with HL and self-reported listening difficulties.
- Conditions
- Hearing Loss
- Being tested
- Practice Listening and Understand Speech (PLUS)
- Keywords
- Auditory Training, Speech Perception, Cognition, Hearing Loss, Listening Difficulties, Intervention
- Medical subject headings
- Hearing Loss
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Practice Listening and Understand Speech (PLUS)Behavioural
Also called PLUS Phonemic Discrimination, PLUS Competing Speech
PLUS is a web-based auditory training platform with two adaptive auditory-cognitive training tasks designed to improve listening and communication.
Phonemic Discrimination:
Phonemes are sounds (e.g. /ba/ vs /da/) that make words different (e.g. "bad" vs "dad"). Participants hear three sounds (e.g., /ba/, /ba/, /da/) from sound pairs (e.g. /ba/ and /da/), and must identify the sound that's different (/da/).
Competing Speech:
Two talkers produce similar sentences that differ by keywords. Participants are asked to focus on one talker (cued by a target visible on screen) while ignoring a second talker and report two keywords from a list of all possible options.
| Study group | Role | What they receive |
|---|---|---|
| Lower perceptual and cognitive demands (Easier) | Experimental | Trainees are asked to train for a minimum of 30 min/day, 5 days/week over a 2-week period (300 minutes in total) and randomly assigned to one of two adaptive tasks, either:
PLUS Phonemic Discrimination (0-back) A 3-interval, 3-alternate forced choice (oddball paradigm) task using eleven phoneme continua (/a/-/uh/, /b/-/d/, /d/-/g/, /e/-/a/, /er/-/or/, /i/-/e/, /l/-/r/, /m/-/n/, /s/-/sh/, /s/-/th/, and /v/-/w/), embedded within syllables, and synthesised from endpoints of real voice recordings. Trainees are asked to respond with the 'odd' sound immediately after presentation of the three stimuli.
Or:
PLUS Competing Speech: (male, female) Based on the Coordinate Response Measure (CRM), based on the Coordinate Response Measure (CRM), real world sentences are spoken by a target and masker that differ in gender. Trainees are asked to report two keywords spoken by the target talker from a list of all options, whilst ignoring the masker talker. Receives: Behavioral: Practice Listening and Understand Speech (PLUS) |
| Higher perceptual and cognitive demands (Harder) | Experimental | Trainees are asked to train for a minimum of 30 min/day, 5 days/week over a 2-week period (300 minutes in total) and randomly assigned to one of two adaptive tasks, either:
PLUS Phonemic Discrimination (1-back) A 3-interval, 3-alternate forced choice (oddball paradigm) task using eleven phoneme continua (/a/-/uh/, /b/-/d/, /d/-/g/, /e/-/a/, /er/-/or/, /i/-/e/, /l/-/r/, /m/-/n/, /s/-/sh/, /s/-/th/, and /v/-/w/), embedded within syllables, and synthesised from endpoints of real voice recordings. Trainees are asked to respond with the 'odd' sound for the three stimuli presented in the prior trial, while holding the 'odd' sound for the current trial in memory.
Or:
PLUS Competing Speech: (female, female) Based on the Coordinate Response Measure (CRM), real world sentences are spoken by a target and masker of the same gender. Trainees are asked to report two keywords spoken by the target talker from a list of all options, whilst ignoring the masker talker. Receives: Behavioral: Practice Listening and Understand Speech (PLUS) |
What is being measured
The primary outcome is the main question the study is designed to answer.
(Adapted) Coordinate Response Measure (CRM)
This test measures how well participants understand target speech when another talker is present. Two sentences are played at the same time: a female talker (target) and a male talker (distracter). Sentences follow the format 'show the [animal] where the [colour] [number] is', using a fixed target animal (dog) and limited sets of colours and numbers. The distractor never says 'dog' and always names a different animal. Participants identify the colour and number spoken by the female talker while ignoring the male talker, responding via computer or touchscreen. Task difficulty is varied by adjusting the signal to noise ratio (SNR) between target and distracter using an adaptive one up/one down staircase to estimate the speech reception threshold (50% correct). Each run ends after a set number of reversals or trials. Participants complete four runs, with the first as practice. Lower thresholds indicate better performance.
Measured: Week 1, Week 3
Secondary outcomes (9)
Practice Listening and Understanding Speech (PLUS) Auditory Training
Performance on the trained PLUS tasks (phonemic discrimination and competing speech) will be measured across the 10 training sessions. Each task uses an adaptive procedure to generate a threshold that reflects the level at which participants correctly identify the target speech information 50% of the time. For phonemic discrimination, this is the smallest contrast between speech sounds that can be reliably distinguished. For competing speech, this is the signal-to-noise ratio needed to understand the target talker. Thresholds from each session indicate learning and changes in trained task performance.
Measured: Week 1, Week 2
Letter N-back
This is a 2-back designed to assess how well participants can keep track of and update information in WM. Letters (A-Z) are presented one at a time, and participants indicate whether the current letter matches the one shown two positions earlier. Each block contains 120 trials: 30 targets (2-back matches) and 90 non-targets. The first two trials are always non-targets. Two distinct versions of the task, each with a different predefined letter sequence, are used to avoid repetition; participants complete one version at pre-training and the alternate version at post-training. Each letter is displayed for 1000 ms within a 2500-ms trial window. Responses are made via keyboard or touchscreen. Accuracy is calculated as correct identification of targets and correct rejection of non-targets, with higher scores indicating better working-memory updating.
Measured: Week 1, Week 3
Flanker Task
This task measures how well participants respond to a central target while ignoring surrounding distractor items. On each trial, a row of fish appears and participants indicate the direction of the middle fish. One practice block (4 trials) and one test block (12 trials) are completed. Each trial begins with a fixation cross (500 ms in practice; 400, 800, or 1200 ms in test trials). Distractor fish then appear for 1150 ms, with the target fish appearing 200 ms later and remaining visible for 750 ms. Participants respond using 'Q'/'P' keys or touchscreen buttons. Feedback is shown for 500 ms. Trials are easier when distractors point the same way as the target and harder when they point the opposite way. Performance is based on response speed and accuracy, with higher scores indicating better ability to manage distracting information.
Measured: Week 1, Week 3
Dual-task of Listening and Memory
Participants complete two tasks at the same time: remembering a sequence of five visually presented digits and repeating spoken words in background noise. Each trial begins with a five-digit string shown for five seconds. Participants then hear five monosyllabic words (AB Isophonemic lists) presented in 0 dB ICRA multitalker babble. Words appear one per screen, beginning 250 ms after screen onset, with the noise continuing for 3000 ms. After typing each word, the next screen appears. Once all five words are entered, participants recall the original five digits. There are four trials in total, with trial order randomised. Scores range from 0-20 for correctly repeated words and 0-20 for correctly recalled digits. Two distinct digit-word lists are used: List 1 is completed in Week 1 (pre-training) and List 2 in Week 2 (post-training).
Measured: Week 1, Week 3
Wisconsin Card Sorting Test (WCST)
This test is designed to assess how well participants can switch their thinking or adapt to new rules and situations. Participants are shown cards that vary in colour, shape, and number and are asked to match a target card to one of four cards displayed above it. The matching rule may relate to colour, shape, or number, but the rule is not given and must be inferred from feedback. Correct responses trigger a green thumbs-up icon and incorrect responses a grey thumbs-down icon, shown for 500 ms. Cards remain on screen until a response is made and feedback is displayed. The rule changes periodically, requiring participants to adjust their choices based on the feedback they receive. Performance is scored by the number of correct sorts and the frequency of perseverative errors, defined as continuing to use a previous rule despite negative feedback. Higher scores indicate better performance on the task.
Measured: Week 1, Week 3
Glasgow Hearing Aid Benefit Profile (GHABP), Part A
Participants are asked to rate their perceived hearing disability (difficulty) and the associated handicap (importance of that difficulty) across four standard listening situations: conversation with one person in quiet, conversation in noise, group conversation, and TV listening. Each is rated on a five-point scale (1 = no difficulty / no importance, 5 = cannot manage at all / very important). Separate mean scores are calculated for Disability and Handicap and expressed as percentages, with higher scores reflecting greater perceived difficulty or handicap. Participants who wear a hearing aid(s) will be asked to complete this questionnaire based on how they hear with their hearing aid(s).
Measured: Week 1, Week 3
Revised Hearing Handicap Inventory (RHHI)
This is a validated self-report instrument designed to measure the perceived psychosocial impact of hearing loss on an individual's daily functioning. The questionnaire comprises 18 items addressing various hearing-related difficulties and emotional responses. Participants respond to each item using a three-point scale: "Yes," "Sometimes," or "No," which are scored 4, 2, and 0 points respectively. The total score ranges from 0 to 72, with higher scores reflecting greater self-perceived hearing handicap. This scoring approach enables the quantification of the degree to which hearing loss affects communication and quality of life, facilitating both clinical assessment and research measurement of hearing-related disability. Participants who wear a hearing aid(s) will be asked to complete this questionnaire based on how they hear with their hearing aid(s).
Measured: Week 1, Week 3
Social Participation Restrictions Questionnaire (SPaRQ)
The Social Participation Restrictions Questionnaire (SPaRQ) is a 19-item, self-report instrument developed to assess the impact of hearing loss on social participation in adults. It comprises two subscales: the 9-item 'Social Behaviors' subscale, which evaluates difficulties in performing social actions due to hearing loss, and the 10-item 'Social Perceptions' subscale, which assesses negative thoughts and feelings experienced in social contexts related to hearing loss. Participants respond to each item using a five-point Likert scale ranging from 'Strongly disagree' to 'Strongly agree'. The total score is the sum of all item scores, with higher scores indicating greater perceived restrictions in social participation. Participants who wear a hearing aid(s) will be asked to complete this questionnaire based on how they hear with their hearing aid(s).
Measured: Week 1, Week 3
Digit Triplets Test
Participants hear triplets of monosyllabic digits (0-9, excluding 7) presented against steady speech-shaped noise in a version of the task rebuilt by the research team in Gorilla. An adaptive 2-up/1-down procedure adjusts the signal-to-noise ratio (SNR) to estimate the speech reception threshold (SRT). The test begins with two fixed trials at 0 dB SNR, then uses step sizes of 8 dB at the first reversal, 4 dB at the second, and 2 dB for the remaining reversals. Exactly 40 trials are administered, with SNRs ranging from -10 to +15 dB. The final SRT is calculated as the average SNR across the last eight reversals, with more negative values indicating better speech-in-noise perception. A cut-off of -5.5 dB SNR or higher is used to identify participants with listening difficulties.
Measured: Week 1
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Apr 2026
- Study start13 Mar 2026
- Primary completion1 Jan 2027 (estimated)
- Study completion1 Feb 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (27)Papers the sponsor has linked to this study.
- Other trials for Hearing LossStudies 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
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Participants are assigned to one of two or more groups in parallel for the duration of the study
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 120 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Nottingham
- Sponsor type
- University, hospital or other
- Collaborators
- National Institute for Health Research, United Kingdom
- Responsible party
- Principal investigator, Helen Henshaw, University of Nottingham
- Investigators
- Helen Henshaw, PhD, Principal investigator, University of Nottingham
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07506408
- Sponsor's protocol ID
- FMHS 245-0925
- Acronym
- PLUS-Optimal
- Status last verified
- Mar 2026
- First submitted
- 19 Mar 2026
- Last updated
- 1 Apr 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Publications
Tsimpida D, Rajasingam S, Panagioti M, Henshaw H. The leaky pipeline of hearing care: primary to secondary care evidence from the English Longitudinal Study of Ageing (ELSA). Int J Audiol. 2024 May;63(5):349-357. doi: 10.1080/14992027.2023.2186814. Epub 2023 Mar 23.
PubMed 36951175Oosthuizen I, Manchaiah V, Launer S, Swanepoel W. Hearing aid Experiences of Adult Hearing aid Owners During and After Fitting: A Systematic Review of Qualitative Studies. Trends Hear. 2022 Jan-Dec;26:23312165221130584. doi: 10.1177/23312165221130584.
PubMed 36300258Ferguson MA, Henshaw H, Clark DP, Moore DR. Benefits of phoneme discrimination training in a randomized controlled trial of 50- to 74-year-olds with mild hearing loss. Ear Hear. 2014 Jul-Aug;35(4):e110-21. doi: 10.1097/AUD.0000000000000020.
PubMed 24752284Henshaw H, McCormack A, Ferguson MA. Intrinsic and extrinsic motivation is associated with computer-based auditory training uptake, engagement, and adherence for people with hearing loss. Front Psychol. 2015 Aug 6;6:1067. doi: 10.3389/fpsyg.2015.01067. eCollection 2015.
PubMed 26300796Boothroyd A. Adult aural rehabilitation: what is it and does it work? Trends Amplif. 2007 Jun;11(2):63-71. doi: 10.1177/1084713807301073.
PubMed 17494873Van Wilderode, M. (2019). The implementation and evaluation of different scenarios for a Dutch auditory-cognitive training scheme [Unpublished doctoral thesis]. KU Leuven.
Stropahl M, Besser J, Launer S. Auditory Training Supports Auditory Rehabilitation: A State-of-the-Art Review. Ear Hear. 2020 Jul/Aug;41(4):697-704. doi: 10.1097/AUD.0000000000000806.
PubMed 31613823Helfer KS, Merchant GR, Wasiuk PA. Age-Related Changes in Objective and Subjective Speech Perception in Complex Listening Environments. J Speech Lang Hear Res. 2017 Oct 17;60(10):3009-3018. doi: 10.1044/2017_JSLHR-H-17-0030.
PubMed 29049601Wright, B. A., & Zhang, Y. (2009). Insights into human auditory processing gained from perceptual learning. In M. S. Gazzaniga, E. Bizzi, L. M. Chalupa, S. T. Grafton, T. F. Heatherton, C. Koch, J. E. LeDoux, S. J. Luck, G. R. Mangan, J. A. Movshon, H. Neville, E. A. Phelps, P. Rakic, D. L. Schacter, M. Sur, & B. A. Wandell (Eds.), The cognitive neurosciences (4th ed., pp. 353-365). Massachusetts Institute of Technology. https://doi.org/10.7551/mitpress/8029.003.0034
Bennett RJ, Laplante-Levesque A, Meyer CJ, Eikelboom RH. Exploring Hearing Aid Problems: Perspectives of Hearing Aid Owners and Clinicians. Ear Hear. 2018 Jan/Feb;39(1):172-187. doi: 10.1097/AUD.0000000000000477.
PubMed 28787315Ferguson MA, Kitterick PT, Chong LY, Edmondson-Jones M, Barker F, Hoare DJ. Hearing aids for mild to moderate hearing loss in adults. Cochrane Database Syst Rev. 2017 Sep 25;9(9):CD012023. doi: 10.1002/14651858.CD012023.pub2.
PubMed 28944461Office for National Statistics. (2019). Population estimates for the UK, England and Wales, Scotland and Northern Ireland: mid-2018. https://www.ons.gov.uk/peoplepopulationandcommunity/populationandmigration/populationestimates/bulletins/annualmidyearpopulationestimates/mid2019estimates
GBD 2019 Hearing Loss Collaborators. Hearing loss prevalence and years lived with disability, 1990-2019: findings from the Global Burden of Disease Study 2019. Lancet. 2021 Mar 13;397(10278):996-1009. doi: 10.1016/S0140-6736(21)00516-X.
PubMed 33714390WHO. (2021) World report on hearing. World Health Organization. https://www.who.int/publications/i/item/9789240020481
Henshaw H, Heinrich A, Tittle A, Ferguson M. Cogmed Training Does Not Generalize to Real-World Benefits for Adult Hearing Aid Users: Results of a Blinded, Active-Controlled Randomized Trial. Ear Hear. 2022 May/Jun;43(3):741-763. doi: 10.1097/AUD.0000000000001096.
PubMed 34524150
Study at a glance
From the registry record, last updated by the sponsor on 1 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- PLUS-Optimal for Adults With Listening Difficulties: Investigating the Roles of Listening and Thinking Skills in Online Training Across Different Groups
- ClinicalTrials.gov ID
- NCT07506408
- Acronym / sponsor ID
- PLUS-Optimal / FMHS 245-0925
- Conditions
- Hearing Loss
- Keywords
- Auditory Training, Speech Perception, Cognition, Hearing Loss, Listening Difficulties, Intervention
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 120 participants (estimated)
- Lead sponsor
- University of NottinghamUniversity, hospital or other
- Collaborators
- National Institute for Health Research, United Kingdom
- Study start
- 13 Mar 2026 (actual)
- Primary completion
- 1 Jan 2027 (estimated)
- Study completion
- 1 Feb 2027 (estimated)
- First posted
- 1 Apr 2026 (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.
WP1: PLUS-Auditory Training
The goal of this experimental study is to better understand how task difficulty affects on-task learning thresholds and generalised benefits in two PLUS auditory training tasks involving perceptual and cognitive learning in adults aged 18+ (no upper age limit) with listening difficulties. The main question it aims to answer is:
- Does adjusting task difficulty in PLUS, by manipulating the perceptual and cognitive demands of the phonemic discrimination and competing speech tasks, affect on-task learning thresholds and off-task performance in adults with listening difficulties?
Researchers will compare the two experimental arms (easy/hard) to see whether adjusting task difficulty influences on-task learning thresholds and off-task performance.
Participants will:
- Be randomly assigned to one of two training programs (phonemic discrimination or competing speech) within the two experimental arms (easy/hard);
- Perform training for a minimum of 30 minutes per day, 5 days per week, for two weeks (total 10 training sessions, 5 hours of training);
- Complete pre- and post- training assessments to measure on-task learning performance and change in performance for untrained measures of speech perception, cognition and self-reported outcomes.
WP2: Post-Training Focus Groups
The goal of this observational study is to gain in-depth qualitative insights into participants' motivations, experiences of task difficulty, and perceived benefits across the PLUS-AT training groups in adults aged 18+ (no upper age limit) with listening difficulties. The main question it aims to answer is:
- How do participants describe their experiences and perceptions of PLUS-AT, particularly regarding task difficulty and self-perceived changes in listening, hearing, thinking, and quality of life?
Researchers will explore participant experiences across the two experimental arms (easy/hard) to determine whether motivations for seeking auditory training, knowledge and beliefs about auditory training, attitudes toward PLUS-AT difficulty, and self-perceived changes in listening, hearing, thinking, and quality of life differ.
A subset of participants (n = 20) will:
- Be invited from WP1 to join one of four online focus groups (60-90 minutes via Microsoft Teams);
- Attend the focus group corresponding to their assigned training program (phonemic discrimination or competing-speech) within the two experimental arms (easy/hard);
- Share their experiences of completing PLUS-AT.
Detailed description
Hearing loss (HL) is a progressive, long-term condition without cure, affecting 18 million people in the UK, which is approximately one in three adults. Globally, HL is the third leading cause of years lived with disability and has major individual, societal, and economic consequences. When unmanaged, HL can lead to communication difficulties, social withdrawal, depression, reduced quality of life, accelerated cognitive decline, and increased dementia risk.
A key challenge reported by people with HL is the difficulty hearing speech in noisy environments, which often persists even when hearing aids (HAs) are used. HAs are the primary management option for HL, but uptake and consistent use is low. Of the 6.7 million people in the UK who could benefit from them, many people do not seek help for their hearing difficulties, and only around 2 million have hearing aids, with non-use estimated to range from 3 to 24%. Therefore, it is essential to develop interventions that can work either as a precursor to or adjacent with HAs to effectively address listening and hearing difficulties.
Auditory training (AT) delivered via internet-accessible devices such as phones or laptops, can be used before or alongside hearing devices such as HAs. As a low-cost intervention, AT supports the self-management of HL and listening difficulties and can be tailored to individual needs. Training itself involves focused listening exercises designed to improve everyday listening, especially in noise. Research shows that AT can improve speech perception throughout an adult's lifespan. It can help individuals improve their ability to distinguish speech in challenging environments like restaurants or family gatherings.
PLUS is a web-based app, standing for Practice Listening and Understanding Speech, developed at the University of Nottingham as an auditory-cognitive training programme. It builds on a decade of research indicating that domain-general improvements in cognitive processing, rather than auditory processing alone, drive the transfer of learning (generalised benefits) to untrained stimuli or tasks. Designed as a cognitively demanding speech training programme, PLUS aims to maximise the transfer of learning to real-world benefits for people with hearing loss. The auditory-cognitive approach was adopted since speech-based tasks are essential for maintaining user motivation and ensuring the training is perceived as relevant to hearing. PLUS has many different settings which changes the task difficulty and influences the level of perceptual and cognitive demand on the learner. It is not known which settings are the most optimal for maximal on-task learning and transfer of learning to everyday listening. The study outlined in this protocol seeks to understand how task difficulty in PLUS affects on-task learning thresholds and generalised benefits in populations with listening difficulties as a first step towards creating an optimal AT intervention for people with HL and self-reported listening difficulties.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
- Model description
- Participants are assigned to one of two or more groups in parallel for the duration of the study
| Arm | Type | Receives |
|---|---|---|
| Lower perceptual and cognitive demands (Easier) | Experimental | Behavioral: Practice Listening and Understand Speech (PLUS)Trainees are asked to train for a minimum of 30 min/day, 5 days/week over a 2-week period (300 minutes in total) and randomly assigned to one of two adaptive tasks, either: PLUS Phonemic Discrimination (0-back) A 3-interval, 3-alternate forced choice (oddball paradigm) task using eleven phoneme continua (/a/-/uh/, /b/-/d/, /d/-/g/, /e/-/a/, /er/-/or/, /i/-/e/, /l/-/r/, /m/-/n/, /s/-/sh/, /s/-/th/, and /v/-/w/), embedded within syllables, and synthesised from endpoints of real voice recordings. Trainees are asked to respond with the 'odd' sound immediately after presentation of the three stimuli. Or: PLUS Competing Speech: (male, female) Based on the Coordinate Response Measure (CRM), based on the Coordinate Response Measure (CRM), real world sentences are spoken by a target and masker that differ in gender. Trainees are asked to report two keywords spoken by the target talker from a list of all options, whilst ignoring the masker talker. |
| Higher perceptual and cognitive demands (Harder) | Experimental | Behavioral: Practice Listening and Understand Speech (PLUS)Trainees are asked to train for a minimum of 30 min/day, 5 days/week over a 2-week period (300 minutes in total) and randomly assigned to one of two adaptive tasks, either: PLUS Phonemic Discrimination (1-back) A 3-interval, 3-alternate forced choice (oddball paradigm) task using eleven phoneme continua (/a/-/uh/, /b/-/d/, /d/-/g/, /e/-/a/, /er/-/or/, /i/-/e/, /l/-/r/, /m/-/n/, /s/-/sh/, /s/-/th/, and /v/-/w/), embedded within syllables, and synthesised from endpoints of real voice recordings. Trainees are asked to respond with the 'odd' sound for the three stimuli presented in the prior trial, while holding the 'odd' sound for the current trial in memory. Or: PLUS Competing Speech: (female, female) Based on the Coordinate Response Measure (CRM), real world sentences are spoken by a target and masker of the same gender. Trainees are asked to report two keywords spoken by the target talker from a list of all options, whilst ignoring the masker talker. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (7 listed)
- Adults (aged 18+ years, no upper age limit);
- Poorer performance on the DTT (SRT of -5.5 dB SNR or higher, as defined by Dawes, 2013) completed without hearing aid(s) for those who typically use them;
- Non-hearing device users or hearing aid(s) owner;
- Ability to read and understand English;
- Ability to provide informed consent;
Key exclusion criteria (3 listed)
- Failure to meet inclusion criteria;
- Having previous auditory training experience;
- Cochlear implant users.
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 |
|---|---|---|
| Practice Listening and Understand Speech (PLUS)Also: PLUS Phonemic Discrimination, PLUS Competing SpeechPLUS is a web-based auditory training platform with two adaptive auditory-cognitive training tasks designed to improve listening and communication. Phonemic Discrimination: Phonemes are sounds (e.g. /ba/ vs /da/) that make words different (e.g. "bad" vs "dad"). Participants hear three sounds (e.g., /ba/, /ba/, /da/) from sound pairs (e.g. /ba/ and /da/), and must identify the sound that's different (/da/). Competing Speech: Two talkers produce similar sentences that differ by keywords. Participants are asked to focus on one talker (cued by a target visible on screen) while ignoring a second talker and report two keywords from a list of all possible options. | Behavioural | Higher perceptual and cognitive demands (Harder), Lower perceptual and cognitive demands (Easier) |
Primary outcome
(Adapted) Coordinate Response Measure (CRM)
Time frame: Week 1, Week 3
This test measures how well participants understand target speech when another talker is present. Two sentences are played at the same time: a female talker (target) and a male talker (distracter). Sentences follow the format 'show the [animal] where the [colour] [number] is', using a fixed target animal (dog) and limited sets of colours and numbers. The distractor never says 'dog' and always names a different animal. Participants identify the colour and number spoken by the female talker while ignoring the male talker, responding via computer or touchscreen. Task difficulty is varied by adjusting the signal to noise ratio (SNR) between target and distracter using an adaptive one up/one down staircase to estimate the speech reception threshold (50% correct). Each run ends after a set number of reversals or trials. Participants complete four runs, with the first as practice. Lower thresholds indicate better performance.
9 secondary outcomes
Practice Listening and Understanding Speech (PLUS) Auditory Training
Time frame: Week 1, Week 2
Letter N-back
Time frame: Week 1, Week 3
Flanker Task
Time frame: Week 1, Week 3
Dual-task of Listening and Memory
Time frame: Week 1, Week 3
Wisconsin Card Sorting Test (WCST)
Time frame: Week 1, Week 3
Glasgow Hearing Aid Benefit Profile (GHABP), Part A
Time frame: Week 1, Week 3
Revised Hearing Handicap Inventory (RHHI)
Time frame: Week 1, Week 3
Social Participation Restrictions Questionnaire (SPaRQ)
Time frame: Week 1, Week 3
Digit Triplets Test
Time frame: Week 1
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Apr 2026.
- Background: PubMed 36951175Tsimpida D, Rajasingam S, Panagioti M, Henshaw H. The leaky pipeline of hearing care: primary to secondary care evidence from the English Longitudinal Study of Ageing (ELSA). Int J Audiol. 2024 May;63(5):349-357. doi: 10.1080/14992027.2023.2186814. Epub 2023 Mar 23.
- Background: PubMed 36300258Oosthuizen I, Manchaiah V, Launer S, Swanepoel W. Hearing aid Experiences of Adult Hearing aid Owners During and After Fitting: A Systematic Review of Qualitative Studies. Trends Hear. 2022 Jan-Dec;26:23312165221130584. doi: 10.1177/23312165221130584.
- Background: PubMed 24752284Ferguson MA, Henshaw H, Clark DP, Moore DR. Benefits of phoneme discrimination training in a randomized controlled trial of 50- to 74-year-olds with mild hearing loss. Ear Hear. 2014 Jul-Aug;35(4):e110-21. doi: 10.1097/AUD.0000000000000020.
- Background: PubMed 26300796Henshaw H, McCormack A, Ferguson MA. Intrinsic and extrinsic motivation is associated with computer-based auditory training uptake, engagement, and adherence for people with hearing loss. Front Psychol. 2015 Aug 6;6:1067. doi: 10.3389/fpsyg.2015.01067. eCollection 2015.
- Background: PubMed 17494873Boothroyd A. Adult aural rehabilitation: what is it and does it work? Trends Amplif. 2007 Jun;11(2):63-71. doi: 10.1177/1084713807301073.
- BackgroundVan Wilderode, M. (2019). The implementation and evaluation of different scenarios for a Dutch auditory-cognitive training scheme [Unpublished doctoral thesis]. KU Leuven.
- Background: PubMed 31613823Stropahl M, Besser J, Launer S. Auditory Training Supports Auditory Rehabilitation: A State-of-the-Art Review. Ear Hear. 2020 Jul/Aug;41(4):697-704. doi: 10.1097/AUD.0000000000000806.
- Background: PubMed 29049601Helfer KS, Merchant GR, Wasiuk PA. Age-Related Changes in Objective and Subjective Speech Perception in Complex Listening Environments. J Speech Lang Hear Res. 2017 Oct 17;60(10):3009-3018. doi: 10.1044/2017_JSLHR-H-17-0030.
- BackgroundWright, B. A., & Zhang, Y. (2009). Insights into human auditory processing gained from perceptual learning. In M. S. Gazzaniga, E. Bizzi, L. M. Chalupa, S. T. Grafton, T. F. Heatherton, C. Koch, J. E. LeDoux, S. J. Luck, G. R. Mangan, J. A. Movshon, H. Neville, E. A. Phelps, P. Rakic, D. L. Schacter, M. Sur, & B. A. Wandell (Eds.), The cognitive neurosciences (4th ed., pp. 353-365). Massachusetts Institute of Technology. https://doi.org/10.7551/mitpress/8029.003.0034
- Background: PubMed 28787315Bennett RJ, Laplante-Levesque A, Meyer CJ, Eikelboom RH. Exploring Hearing Aid Problems: Perspectives of Hearing Aid Owners and Clinicians. Ear Hear. 2018 Jan/Feb;39(1):172-187. doi: 10.1097/AUD.0000000000000477.
- Background: PubMed 28944461Ferguson MA, Kitterick PT, Chong LY, Edmondson-Jones M, Barker F, Hoare DJ. Hearing aids for mild to moderate hearing loss in adults. Cochrane Database Syst Rev. 2017 Sep 25;9(9):CD012023. doi: 10.1002/14651858.CD012023.pub2.
- BackgroundOffice for National Statistics. (2019). Population estimates for the UK, England and Wales, Scotland and Northern Ireland: mid-2018. https://www.ons.gov.uk/peoplepopulationandcommunity/populationandmigration/populationestimates/bulletins/annualmidyearpopulationestimates/mid2019estimates
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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.
Helen Henshaw, PhD principal investigator
University of Nottingham
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Practice Listening and Understand Speech (PLUS) in people with Hearing Loss, run by University of Nottingham at 1 site in United Kingdom.
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 7 inclusion and 3 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: looking for participants now, as of the sponsor's last update on 1 Apr 2026. 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 United Kingdom. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Natalie Lerigo-Smith, MSc (+44 (0)115 8232600, natalie.lerigo-smith1@nottingham.ac.uk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
(Adapted) Coordinate Response Measure (CRM) (time frame: Week 1, Week 3). 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 NCT07506408, which also lists 27 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 Apr 2026.