Skip to content

A study on home intervention strategies for hearing aids in older adults at high risk of dementia and its impact on cognitive function

A study on home intervention strategies for hearing aids in older adults at high risk of dementia and its impact on cognitive function

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091791
Enrollment
Unknown
Registered
2024-11-04
Start date
2024-11-07
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Mild cognitive impairment, hearing loss

Interventions

Intervention group:Hearing aid use, family empowerment autonomy motivation support intervention, and health education on hearing aid skills
Control group:Hearing aid use and regular health education

Sponsors

Peking University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: Participants should meet all of the following conditions: 1.Participants aged between 60 and 85 years old; 2. The pure-tone average (PTA) of the participants' better ear at 500, 1k, 2k, and 4kHz was between 35-80db HL (excluding 80); 3. Participants were diagnosed with mild cognitive impairment according to the Montreal Cognitive Assessment to Hearing Impairment (MOCA-HI scored above 18 and below 26); 4. Participants were diagnosed with sensorineural hearing loss based on history of ear diseases, pure tone audiometry, and tympanometry. They were also diagnosed as post-lingual hearing loss; 5. Participants can understand the complete the intervention plan and the outcome assessment scales; 6. Participants wore their hearing aids for less than three months; 7. Participants have support from their family members; 8. Participants sign an informed consent form and participated voluntarily.

Exclusion criteria

Exclusion criteria: Participants who meet any of the following conditions will be excluded: 1. Participants were diagnosed with congenital hearing loss or permanent conductive hearing loss; 2. Participants were diagnosed with asymmetrical hearing loss (the difference in PTA between two ears was 30 db HL and above); 3. Participants have vision loss (visual acuity was less than 20/63 assessed by the Snellen scale, equivalent to being unable to comfortably read size 14 font); 4. Participants have medical contraindications for hearing aid use (such as progressive or fluctuating hearing loss, sudden sensorineural hearing loss within the past three months, accompanied by otorrhea, ear pain, dizziness or headache, congenital or traumatic ear deformity, etc.); 5. Participants are engaging in another intervention project currently.

Design outcomes

Primary

MeasureTime frame
Cognitive function;

Secondary

MeasureTime frame
Adherence of hearing aid use;Severity of hearing loss;Outcome for hearing aids;Hearing aid skills;Activities of daily life (ADL);Quality of life;Depressive symptoms;Subjective cognitive decline;Social support;Self-efficacy;Healthcare utilization;Autonomy motivation support;Family caregiver burden;Motivation of hearing aid use;

Countries

China

Contacts

Public ContactYanan Luo

Department of Global Health, School of Public Health, Peking University

luoyanan@bjmu.edu.cn+86 10 8280 6537

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 21, 2026