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Effects of the Swedish Internet-based Individualised Active Communication Education (I-ACE) in FTU

Effects of the Swedish Internet-based Individualised Active Communication Education (I-ACE) in First Time Hearing Aid Users: a Randomised Controlled Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05815667
Acronym
I-ACE
Enrollment
63
Registered
2023-04-18
Start date
2023-03-01
Completion date
2023-12-16
Last updated
2025-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hearing Impairment

Brief summary

Hearing impairment affects the ability to communicate, which can adversely affect both mental and physical health. The most common used rehabilitation method in hearing impairment is hearing aid fitting. Even with optimally fitted hearing aids, many struggle to hear in situations with difficult listening conditions. Active Communication Education (ACE) is an interactive group rehabilitation programme aiming to help those with hearing loss communicate more effectively using communication strategies to cope better in everyday life. An Individualised Active Communication Education (I-ACE) distributed digitally could enable those unable to get to the hearing care facility, or don't want to join the group sessions to benefit from the programme. This project aims to investigate the effects of the swedish digital version of the I-ACE in first time hearing aid users.

Interventions

BEHAVIORALIndividualised Active Communication Education (I-ACE)

The swedish I-ACE consists of five modules with different themes, all with sections of information alternated with reflective tasks. The participants are assigned one module each week and provided with weekly feedback from a health care professional on their work, before being assigned the next module.

Sponsors

Horselvarden Region Ostergotland
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults \>20 years old who have been fitted with hearing aids for the first time (first time users) 6 - 12 months prior. * Computer experience and access to computer, tablet and/or smartphone with internet access. * Access to BankID or equivalent.

Exclusion criteria

* Those who have participated in Active Communication Education prior.

Design outcomes

Primary

MeasureTime frameDescription
Communication and Acceptance Scale (CAS)Baseline, directly post intervention and 6 months post intervention.Assessing changes in use of communication strategies and the emotional consequences, knowledge and acceptance of hearing loss. Minimum 18 points to maximum 90. Higher score indicates a lower impact of the hearing loss.

Secondary

MeasureTime frameDescription
Communication Strategies Scale (CSS)Baseline, directly post intervention and 6 months post intervention.Assessing changes in use of verbal, non-verbal and maladaptive communication strategies. Minimum 25 points to maximum 100. Higher score indicates a greater use of communication strategies.
The Hearing Handicap Inventory for the Elderly (HHIE)Baseline, directly post intervention and 6 months post intervention.Assessing changes in emotional and social effects of hearing loss. Minimum 0 points to maximum 100 points. Higher score indicates greater emotional and social effects of hearing loss.
The International Outcome Inventory for Hearing Aids (IOI-HA)Baseline, directly post intervention and 6 months post intervention.Assessing changes in perceived effectiveness and satisfaction with hearing aids. Minimum 7 points to maximum 35 points. Higher score indicates higher perceived effect.
The International Outcome Inventory for Alternative Interventions (IOI-AI)Directly post intervention and 6 months post intervention.Assessing changes in perceived effectiveness with an alternative intervention, in this case the I-ACE. Minimum 7 points to maximum 35 points. Higher score indicates higher perceived effect.

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026