Skip to main content
UK clinical trials - updated daily from ClinicalTrials.gov
TrialConnect
← Back to Search
Looking for participantsNA

Evaluating an Audiology Text-Message Protocol to Support Hearing Aid Use in NHS Adult Audiology Patients

Sponsor: WSAUD A/S

NCT ID: NCT07146607

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Audiology text-message protocol (behavioural)
How long the study runs
Study runs about 15 months (dates as stated)
About the drug or intervention
Audiology text-message protocol — behavioural: Florence is an interactive text messaging service, endorsed by NHS England, designed to improve clinical outcomes for patients.
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years and over
Who
All
Number of participants
70
Started
2025-09-30
Last checked
2026-03

Plain English Summary

What is this study?

  • • Testing a new treatment for hearing loss
  • • NA - 70 participants
  • • Over 18 million adults in the United Kingdom have significant hearing loss, linked to isolation, depression and comorbidities

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with hearing loss

Where?

  • • Nottingham - QMC Ropewalk House
  • • Sunderland - Sunderland Royal Hospital, Kayll Road, Sunderland, SR4 7TP
  • • Wigan - Audiology Department Suite 2 Thomas Linacre Centre Parsons Walk Wigan WN1 1RU

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

Over 18 million adults in the United Kingdom have significant hearing loss, linked to isolation, depression and comorbidities. Hearing aids are the main management option yet are frequently unused (\~23%) or used irregularly (\<40%), wasting NHS resources and reducing quality-of-life gains. Digital behaviour-change interventions can improve self-management between appointments. Florence, an NHS-endorsed text-messaging system, has been used in the management of other long-term conditions, but has not yet been applied within audiology. This study will test a standardised audiology text-message protocol, delivered via Florence, to support new NHS hearing aid users, aiming to improve adherence, outcomes, and cost-effectiveness. Outcomes assess trial feasibility (primary objective), proof-of concept for efficacy (secondary objective), and process evaluation (tertiary objective).

More detail

Over 18 million adults in the UK have significant hearing loss, with prevalence and severity increasing with age. Hearing loss is a leading global cause of disability, associated with social isolation, depression, dementia, and reduced quality of life, and is more common among people with other long-term conditions such as diabetes, hypertension, and cardiovascular disease. Hearing aids are the standard clinical management, yet up to 23% of new users abandon them and \<40% use them irregularly, resulting in wasted NHS resources and prolonging hearing difficulties. Adjusting to hearing aids is a novel health behaviour, and behaviour-change interventions informed by health psychology can empower patients to manage their care, benefiting both patients and healthcare systems. Digital interventions, such as mobile text-messaging, are cost-effective ways to provide information and support between appointments and improve self-management. Florence, an NHS-endorsed text-messaging system, has improved self-management in long-term conditions including hypertension, diabetes, and cancer, improving patient satisfaction and cost-effectiveness. It has not yet been applied in audiology. This feasibility study will examine a standardised audiology text-message protocol, delivered via Florence, for new NHS hearing aid users, addressing trial feasibility, proof-of-concept, and process evaluation objectives. Effective use could improve hearing aid adherence, quality of life, and save the NHS millions annually.

Hearing Loss

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

Treatment history

Treatments you must have had:

  • ✓ to be a smart phone device)

What the study is looking for

  • ✓WP1: Pilot Feasibility Study (n=60, 30 per group intervention/control (treatment as usual)) Inclusion criteria
  • ✓Aged ≥18 years (no upper age limit)
  • ✓Prescribed their first NHS acoustic hearing aid(s) for the primary concern of hearing loss
  • ✓Able and willing to provide agreement to take part
  • ✓Not currently participating in similar research
See the full criteria
WP1: Pilot Feasibility Study (n=60, 30 per group intervention/control (treatment as usual)) Inclusion criteria * Aged ≥18 years (no upper age limit) * Prescribed their first NHS acoustic hearing aid(s) for the primary concern of hearing loss * Able and willing to provide informed consent * Not currently participating in similar research * Access to a mobile device (This is not required to be a smart phone device) Exclusion criteria * Registered on a pre-existing Florence text-messaging protocol. * Unable to read/understand English WP2: Nested Process Evaluation (minimum n=10 patients, n=2 clinicians) Inclusion criteria (patients) * Aged ≥18 years (no upper age limit) * Prescribed their first NHS acoustic hearing aid(s) for the primary concern of hearing loss * Able and willing to provide informed consent Exclusion criteria (patients) * Registered on a pre-existing Florence text-messaging protocol. * Unable to read/understand English Inclusion criteria (clinicians) * Aged ≥18 years (no upper age limit) * Able and willing to provide informed consent Exclusion criteria (clinicians) • Not meeting criteria for inclusion

Where Is This Study? (3 UK sites)

QMC Ropewalk House

Nottingham NG1 5DU, United Kingdom

ENROLLING_BY_INVITATION

Sunderland Royal Hospital, Kayll Road, Sunderland, SR4 7TP

Sunderland SR4 7TP, United Kingdom

Recruiting

Audiology Department Suite 2 Thomas Linacre Centre Parsons Walk Wigan WN1 1RU

Wigan WN1 1RU, United Kingdom

Recruiting

How to Get in Touch

Emma E Broome, PhD

Sponsor contact

CONTACT

+44 (0) 115 8232606 emma.broome1@nottingham.ac.uk

Helen Henshaw, PhD

Sponsor contact

CONTACT

+44 (0) 115 8232606 helen.henshaw@nottingham.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2026-03