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Remote programming for bone anchored hearing aid users

Remote Assist for bone anchored hearing aid users

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-632fptj
Enrollment
Unknown
Registered
2025-10-01
Start date
2025-05-12
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Conductive hearing loss

Interventions

This is a prospective, non-randomized, single-arm, open-label clinical study. The study will include a total of 200 adult participants who are users of bone-anchored hearing aids (BAHA) with either pe
(2) assessment of device use
(3) possible programming adjustments
and (4) guidance on usage. At the end of the session, participants will complete a satisfaction and usability questionnaire. A 1-month follow-up will be conducted to reassess clinical and functional d
L01.462.500.847.652
E07.695.118

Sponsors

Hospital de Reabilitação de Anomalias Craniofaciais da Universidade de São Paulo (HRAC-USP)
Lead Sponsor
Hospital de Reabilitação de Anomalias Craniofaciais da Universidade de São Paulo (HRAC-USP)
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Adult users of bone-anchored hearing aids with the Baha Connect or Baha Attract system; Minimum and maximum age without limit; both genders; minimum three months of experience using the device; access to a smartphone compatible with the Remote Assist app; availability to participate in the scheduled in-person and remote sessions

Exclusion criteria

Exclusion criteria: Individuals with intellectual disabilities or psychiatric disorders that prevent autonomous use of the application; lack of connectivity or compatible devices; diagnosis of hearing loss not indicated for use of the Baha system; non-adherence to the remote protocol

Design outcomes

Primary

MeasureTime frame
To assess the feasibility of using Cochlear's Remote Assist remote care feature for Baha system users, using systematic records during remote care sessions and specific satisfaction and usability questionnaires

Secondary

MeasureTime frame
Verify the effectiveness of the remote protocol in maintaining functional gain parameters in the free field. To this end, a new audiological assessment will be performed before and after the remote sessions, including a speech perception test (HINT) and free-field measurements

Countries

Brazil

Contacts

Public ContactCarlos Alberto Santana Júnior

Hospital de Reabilitação de Anomalias Craniofaciais da Universidade de São Paulo (HRAC-USP)

carlosfono@usp.br+55(79)99966-7915

Outcome results

None listed

Source: REBEC (via WHO ICTRP)