MedPath

mHealth Technologies for Hearing Aid Users

Completed
Conditions
Hearing Loss
Interventions
Other: Mobile-enabled RLOs (mRLOs)
Registration Number
NCT03136718
Lead Sponsor
Nottingham University Hospitals NHS Trust
Brief Summary

This study will establish the feasibility of a theoretically-driven, personalised educational intervention delivered through mobile technologies in first-time hearing aid users. Namely, the C2Hear (https://www.youtube.com/C2HearOnline) multimedia videos, or Reusable Learning Objects (RLOs) (Ferguson et al., 2015; 2016), will be repurposed into short 'bite-sized' mobile-enabled RLOs (mRLOs).The development of the intervention will be based on a recently developed comprehensive model of health behaviour change (COM-B) (Michie et al., 2014). The intervention will be tailored to individuals' needs, and incorporate greater user interactivity and self-evaluation.

Detailed Description

Research question: Is it feasible for first-time hearing aid users to use a personalised educational intervention delivered through mobile technologies in their everyday life?

Objectives: To establish the feasibility of the intervention by evaluating delivery, accessibility, usability, acceptability, and adherence in first-time hearing aid users. To establish suitable outcome measures to evaluate the effectiveness of the intervention in a future randomised controlled trial.

Study Design: Single centre, feasibility.

Naïve first-time hearing aid users will try out the intervention away from the laboratory. Following 10-12 weeks of independent use, the investigators will assess how the participants used the intervention using a mixed-methods approach across two parallel stages:

Stage 1. The investigators will assess the feasibility of the intervention in first-time hearing aid users, who will be invited to take part in semi-structured interviews. Using the COM-B model (Michie et al., 2014) as the framework underpinning the interviews, delivery, accessibility, usability, acceptability, and adherence of the intervention will be evaluated. Transcribed audio-recordings will be analysed using thematic analysis (Braun \& Clarke, 2006). A total of 15 participants is typically sufficient to achieve data saturation (the point in data collection when no new information emerges) using this qualitative methodology (Guest et al., 2006). To allow for 18% attrition (Ferguson et al., 2016), 18 patients will be. To prevent potential confounding of the interviews, participants will not be required to complete quantitative outcome measures used in stage 2.

Stage 2. The investigators will assess which outcome measures are suitable to assess the intervention in terms how well it supported users to make changes to their behaviour. First-time hearing aid users will complete outcome measures by interview. Outcomes were selected based on the World Health Organisation's International Classification of Functioning, Disability and Health (ICF) (WHO, 2001), which provides a theoretical framework upon which to measure the success of amplification using hearing aids. At least 50 participants are required to allow for sufficient between- and within-subject variability in order to calculate important change scores for each outcome measure. To allow for 18% attrition 59 patients will be recruited.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
94
Inclusion Criteria
  • First-time hearing aid users (or if previous users, but not having worn hearing aids for more than 3 years)
  • Familiar with mobile technologies (e.g. owns a smartphone or tablet device, or uses one regularly)
  • English as a first spoken language or a good understanding of English. It is important that participants can understand the content of the resources and work with the interactive elements, as well as be able to answer outcome questionnaires, to ensure valid data are collected.
Exclusion Criteria
  • Unable to complete the questionnaires without assistance due to age-related problems (e.g. cognitive decline or dementia), to ensure valid data are collected.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
First-time hearing aid usersMobile-enabled RLOs (mRLOs)Individuals using hearing aids for the first-time (or if previous users, have not having worn hearing aids for more than 3 years) will have access to the mobile-enabled RLOs (mRLOs) intervention, which will be given to the participants shortly after their hearing aid is fitted.
Primary Outcome Measures
NameTimeMethod
Glasgow Hearing Aid Benefit Profile (GHABP: Gatehouse, 1999) - Hearing aid useFollowing 10-12 weeks of independent use of the mRLO intervention

Self-reported hearing aid use measured on a five-point scale.

Secondary Outcome Measures
NameTimeMethod
Glasgow Hearing Aid Benefit Profile (GHABP)Baseline (Part I) and following 10-12 weeks of independent use of the mRLO intervention (Part II)

Assesses hearing disability (or activity limitations) and handicap (or participation restrictions; part 1), and hearing aid use, benefit, residual disability and satisfaction (part 2). Each domain is measured on a five-point scale.

Hearing Handicap Inventory for the Elderly (HHIE: Ventry & Weinstein, 1982)Baseline and following 10-12 weeks of independent use of the mRLO intervention

25-item questionnaire designed to assess the effects of hearing loss on the emotional (n = 13), and social/situational adjustment (n = 12) of older people, scored using a three-point scale (4 = yes; 2 = sometimes; 0 = no).

Hearing aid dataloggingFollowing 10-12 weeks of independent use of the mRLO intervention

Hearing aid use in hours internal to the hearing aid

Social Participation Restrictions Questionnaire (SPaRQ: Heffernan et al., 2015)Baseline and following 10-12 weeks of independent use of the mRLO intervention

A 19-item inventory that assesses social behaviors (9-items) and perceptions (10-items) in adults with mild-to moderate hearing loss. Each item is measured on an 11-point response scale ranging from 'Completely Disagree' at point zero to 'Completely Agree' at point ten.

Measure of Audiologic Rehabilitation Self-efficacy for Hearing Aids (MARS-HA: West & Smith, 2007)Baseline and following 10-12 weeks of independent use of the mRLO intervention

Includes four subscales: basic handling, advanced handling, adjustment to hearing aids, and aided listening skills.

Respondents indicate how confident they are that they could do the things described on an 11-point scale (0%=cannot do this, to 100%=certain I can do this).

Hearing Aid and Communication Knowledge (HACK: Ferguson et al., 2015)Baseline and following 10-12 weeks of independent use of the mRLO intervention

A 20-item open-ended questionnaire that measures free recall of knowledge relevant to practical (n = 12) and psychosocial (n = 8) issues on hearing aids and communication.

Clinical Global Impression Scale - Hearing difficultiesBaseline and following 10-12 weeks of independent use of the mRLO intervention

A one item questionnaire to be used to identify the minimal important change score specific to each self-reported outcome measure.

Wechsler Adult Intelligence Scale (WAIS) - Digit Span (Wechsler, 1997)Baseline and following 10-12 weeks of independent use of the mRLO intervention

Cognitive measure of memory recall

Trial Locations

Locations (1)

National Institute for Health Research Nottingham Biomedical Research Centre

🇬🇧

Nottingham, Non-US/Non-Canadian, United Kingdom

© Copyright 2025. All Rights Reserved by MedPath