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Follow Up of an Online Hearing Support for First-time Hearing Aid Users

Follow Up of an Online Hearing Support for First-time Hearing Aid Users Using the Swedish I-ACE, Clinical Visit or Nothing

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06468137
Enrollment
100
Registered
2024-06-21
Start date
2024-07-01
Completion date
2026-12-31
Last updated
2026-08-12

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

Conditions

Hearing Disorders, Hearing Impairment, Hearing Loss

Brief summary

The main questions the research aims to answer are short- and long-term effects on consequences of hearing loss depending on which type of follow-up the participant chooses.

Detailed description

Investigation of the emotional and social consequences of hearing loss that the participants experience, use of communications strategies, experienced listening in complex sound environments and perceived effectiveness and satisfaction with hearing aids. The goal is also to assess changes in use of communication strategies and the emotional consequences, knowledge and acceptance of hearing loss.

Interventions

BEHAVIORALSwedish I-ACE

Rehabilitative programme with focus on communication strategies and problem solving for people with hearing loss.

BEHAVIORALClinical visit

Visit in the clinic with focus on audiologic rehabilitation.

Participants choosing no follow-up.

Sponsors

Region Skane
Lead SponsorOTHER
Horselvarden Region Ostergotland
CollaboratorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* People who have participated in NCT06051968 are automatically enrolled to participate in the follow-up according to the study protocol.

Design outcomes

Primary

MeasureTime frameDescription
The Hearing Handicap Inventory for the Elderly (HHIE)Baseline, about 7 weeks post choice of intervention, and 6 months post interventionAssessing changes in emotional and social effects of hearing loss, self-perceived activity limitations and participation restrictions. Minimum 0 points to maximum 100 points. Higher score indicates greater emotional and social effects of hearing loss.

Secondary

MeasureTime frameDescription
The 12-item Speech, Spatial and Qualities of Hearing Scale (SSQ12)Baseline, about 7 weeks post choice of intervention, and 6 months post interventionAssessing experience of listening in complex sound environments. Minimum 0 points to 120 points. Higher score indicates less problems with hearing in the specified situations.
Communication Strategies Scale (CSS)Baseline, about 7 weeks post choice of intervention, and 6 months post interventionAssessing changes in use of verbal, non-verbal and maladaptive communication strategies. Minimum 25 points to maximum 125 points. Higher score indicates a greater use of communication strategies.
The International Outcome Inventory for Hearing Aids (IOI-HA)Baseline, about 7 weeks post choice of intervention, and 6 months post interventionAssessing changes in perceived effectiveness and satisfaction with hearing aids. Minimum 7 points to maximum 35 points. Higher score indicates higher perceived effect.
Communication and Acceptance Scale (CAS)Baseline, about 7 weeks post choice of intervention, and 6 months post interventionAssessing 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.
The International Outcome Inventory for Alternative Interventions (IOI-AI)Baseline, about 7 weeks post choice of intervention, and 6 months post interventionAssessing changes in perceived effectiveness and satisfaction with an alternative intervention, in this case the Swedish I-ACE. Minimum 7 points to maximum 35 points. Higher score indicates higher perceived effect.

Countries

Sweden

Contacts

PRINCIPAL_INVESTIGATORMarie Öberg

Horselvarden Region Ostergotland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 13, 2026