Effect of Donepezil on Speech Recognition in Cochlear Implant Users

NCT ID: NCT05438264

Last Updated: 2025-10-02

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: EARLY_PHASE1
• Total Enrollment: 50 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-03-10
• Study Completion Date: 2026-09-01

Brief Summary

Hearing loss is a major cause of disability that affects over 48 million Americans. There are currently no medications used to treat sensorineural hearing loss. Cochlear implants can significantly restore hearing in adults with moderate to profound sensorineural hearing loss, but their utility is limited by the wide variability in hearing outcomes. Differences in cochlear implant outcomes may be explained by neuroplasticity, as neural networks must reorganize to process the new auditory information provided by the implant.

The investigators predict that cholinergic enhancement with donepezil (an acetylcholinesterase inhibitor) may facilitate cortical reorganization in cochlear implant users, leading to functional improvements in speech recognition and cognition. In addition to taking donepezil, study participants will be asked to increase their daily processor use. Studies suggest that increasing daily device use can improve speech recognition, and this study will explore whether this effect can be augmented further with donepezil.

In this randomized, double-blind controlled trial, the investigators aim to assess the effects of donepezil on speech recognition, cortical plasticity, and cognition. Participants will start daily treatment with either donepezil 5 mg or placebo. Participants will be followed longitudinally at 1 month and 3 months after starting the study. The findings from this study will provide important insight into the mechanisms of hearing restoration and could potentially improve hearing and cognitive outcomes for future cochlear implant users.

Detailed Description

The proposed study is a double-blind, randomized controlled trial comparing donepezil with placebo in adult cochlear implant users.

Aim 1: Evaluate if donepezil treatment improves speech recognition in cochlear implant users.

Aim 2: Evaluate if donepezil treatment increases intramodal auditory cortex activity in cochlear implant users.

Aim 3: Evaluate if donepezil treatment improves cognition in cochlear implant users.

Conditions

Bilateral Sensorineural Hearing Loss

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Experimental

Donepezil 5 mg, daily

Group Type: EXPERIMENTAL

Donepezil

Intervention Type: DRUG

acetylcholinesterase inhibitor

Control

Placebo, daily

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

placebo

Interventions

Donepezil

acetylcholinesterase inhibitor

Intervention Type: DRUG

Placebo

placebo

Intervention Type: DRUG

Other Intervention Names

Aricept

Eligibility Criteria

Inclusion Criteria

1. At least 6 months of cochlear implant use

2. Age ≥ 18 years

3. Post-lingual onset of deafness

4. Audiometric thresholds meeting FDA-labeled indications for adult cochlear implantation

5. Normal or corrected-to-normal vision assessed with a Snellen eye chart

6. English verbal communication

7. No participation in any other clinical trial within the past 3 months

8. Physically healthy

9. Female participants must have no child-bearing potential or agree to practice effective contraception during the study (such as established use of oral, injected or implanted hormonal methods of contraception; placement of an intrauterine device or intrauterine system; condom with spermicidal foam/gel/film/cream/suppository; occlusive cap with spermicidal foam/gel/film/cream/suppository; male partner sterilization; or true abstinence when this is in line with the preferred and usual lifestyle of the subject)

10. Female participants of child-bearing potential must have a negative urine pregnancy test at the time of enrollment and before each study visit

Exclusion Criteria

1. Evidence of conductive hearing loss

2. Diagnosed neurological or sensory disorder (such as Alzheimer's disease, Parkinson's disease, epilepsy, stroke, autism, schizophrenia, or uncorrected visual impairment)

3. Positive urine pregnancy test at any time during the study

4. Breastfeeding or nursing at any time during the study

5. Known hypersensitivity to donepezil hydrochloride or to piperidine derivatives

6. Current use of medications with known anticholinergic effects (such as tricyclic antidepressants, first-generation antihistamines, or bladder antispasmodics)

7. Current or prior use of cholinesterase inhibitors

8. Use of tobacco or nicotine products in the past 1 month

9. Severe anatomic abnormalities of the temporal bone

10. Major active life-threatening illness

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 100 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Vanderbilt University Medical Center

OTHER

Sponsor Role: lead

Responsible Party

Aaron Moberly

Professor, Otolaryngology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

René Gifford, PhD

Role: PRINCIPAL_INVESTIGATOR

Vanderbilt University Medical Center

Mark Wallace, PhD

Role: PRINCIPAL_INVESTIGATOR

Vanderbilt University

Aaron Moberly, MD

Role: PRINCIPAL_INVESTIGATOR

Vanderbilt University Medical Center

Locations

Vanderbilt University Medical Center

Nashville, Tennessee, United States

Countries

United States

Other Identifiers

220844

Identifier Type: -

Identifier Source: org_study_id