Early Age-Related Hearing Loss Investigation Pilot Study (P-EARLHI)
Primary Purpose
Hearing Loss
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Phonak Audeo Lumity Receiver in Canal Hearing Aid
Sponsored by
About this trial
This is an interventional treatment trial for Hearing Loss
Eligibility Criteria
Inclusion Criteria: Adults aged 55 to 75 years old with little or no experience with hearing aids English or Spanish speakers Exclusion Criteria: Unable to complete written questionnaires on a tablet without assistance Refer for cognitive screening score based on criteria using the Mini Mental State Examination
Sites / Locations
- University of South FloridaRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Hearing Intervention Group
Arm Description
Adults aged 55-75 with hearing loss who have little/no prior experience with hearing aids will be enrolled in the hearing intervention group.
Outcomes
Primary Outcome Measures
Objective Physical Activity
Activity level as measured by research-grade accelerometer
Secondary Outcome Measures
Words in Noise Test
Measures speech perception in noise performance
International Outcome Inventory for Comprehensive Hearing Intervention
Self-reported hearing aid benefit measure
Client Oriented Scale of Improvement
Self-reported hearing aid benefit measure
Hearing Handicap Inventory for Adults
Self-reported hearing handicap
Center for Epidemiological Studies Depression and Hopelessness Scale
Self-reported depression
Speech, Spatial and Qualities of Hearing Scale
Self-reported hearing difficulties
Social Network Index
Self-reported social network information
UCLA Loneliness Scale
Self-reported loneliness
The Positive and Negative Affect Schedule
Self-reported positive and negative affect/mood
The World Health Organization Well-Being Index
Self-reported well being
The Vanderbilt Fatigue Scale for Adults
Self-reported fatigue
Research & Development Short Form Survey (RAND36)
Self-reported quality of life
Single-item sedentary questionnaire
Self-reported physical activity
Modified four-square step test
Measures physical function
Expanded short physical performance battery
Measures lower extremity function
Baecke Physical Activity Questionnaire
Self-reported physical activity
PROMIS v2.0 Mobility Questionnaire
Self-reported mobility
User Experience Questionnaire+
Self-reported hearing device user experience
Full Information
NCT ID
NCT05970211
First Posted
July 6, 2023
Last Updated
July 24, 2023
Sponsor
University of South Florida
1. Study Identification
Unique Protocol Identification Number
NCT05970211
Brief Title
Early Age-Related Hearing Loss Investigation Pilot Study
Acronym
P-EARLHI
Official Title
Early Age-Related Hearing Loss Investigation Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 19, 2023 (Actual)
Primary Completion Date
April 15, 2024 (Anticipated)
Study Completion Date
August 15, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of South Florida
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this clinical trial pilot is to obtain feasibility and pilot data necessary to inform the hearing intervention being designed for a larger R01 clinical trial that seeks to determine whether best practice hearing aid intervention impacts hearing-related outcomes in adults with hearing loss aged 55 to 75 years.
Secondary purposes include: To determine what effects best practice hearing aid intervention has on physical, social, and quality of life outcomes in adults with hearing loss aged 55 to 75 years.
Detailed Description
This is an observational pre-post intervention feasibility study. In addition to the objective finding that adults with hearing loss experience higher rates of cognitive decline, they also tend to report lesser degrees of physical activity and increased cognitive fatigue, which is the feeling of tiredness or having a lack of energy. Unfortunately, the mechanism by which hearing loss relates to physical activity and fatigue, and the effect of hearing aids as an intervention to improve these factors, is unclear. Thus, the purpose of this study is twofold: First, we will establish the feasibility of administering a best practices hearing aid intervention to a sample of adults from the target age range of 55 - 75 years old to inform the larger clinical trial; Second, we will collect pilot data to explore the relationships between hearing loss, physical activity, socialization, fatigue and hearing-related outcomes before and after hearing aid intervention.
There are no experimental or investigational devices or agents used in this study. We are providing best-practices standard of care hearing intervention including hearing aids. We are additionally tracking activity using the ActiGraph wGT3X-BT, an FDA-approved Class II medical device that tracks continuous, high resolution physical activity and sleep/wake information.
Participation involves a minimum of 6 in-office study visits. Intervention sessions occur approximately 2 weeks apart, with a final long-term outcome session occurring approximately 6-months post the baseline intervention session.
Significant others of participants are invited to join the study and contribute data related to their own quality of life and their observations of the effects of the hearing intervention on the participant.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hearing Loss
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Hearing Intervention Group
Arm Type
Experimental
Arm Description
Adults aged 55-75 with hearing loss who have little/no prior experience with hearing aids will be enrolled in the hearing intervention group.
Intervention Type
Device
Intervention Name(s)
Phonak Audeo Lumity Receiver in Canal Hearing Aid
Intervention Description
bilateral receiver in canal hearing aids provided as part of a best practices hearing loss intervention including devices, hearing centered counseling, and self management skills training for hearing loss
Primary Outcome Measure Information:
Title
Objective Physical Activity
Description
Activity level as measured by research-grade accelerometer
Time Frame
2-week measurement taken between 4- and 6- months post study enrollment
Secondary Outcome Measure Information:
Title
Words in Noise Test
Description
Measures speech perception in noise performance
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
Title
International Outcome Inventory for Comprehensive Hearing Intervention
Description
Self-reported hearing aid benefit measure
Time Frame
Measured at 6-months post study enrollment
Title
Client Oriented Scale of Improvement
Description
Self-reported hearing aid benefit measure
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
Title
Hearing Handicap Inventory for Adults
Description
Self-reported hearing handicap
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
Title
Center for Epidemiological Studies Depression and Hopelessness Scale
Description
Self-reported depression
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
Title
Speech, Spatial and Qualities of Hearing Scale
Description
Self-reported hearing difficulties
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
Title
Social Network Index
Description
Self-reported social network information
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
Title
UCLA Loneliness Scale
Description
Self-reported loneliness
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
Title
The Positive and Negative Affect Schedule
Description
Self-reported positive and negative affect/mood
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
Title
The World Health Organization Well-Being Index
Description
Self-reported well being
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
Title
The Vanderbilt Fatigue Scale for Adults
Description
Self-reported fatigue
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
Title
Research & Development Short Form Survey (RAND36)
Description
Self-reported quality of life
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
Title
Single-item sedentary questionnaire
Description
Self-reported physical activity
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
Title
Modified four-square step test
Description
Measures physical function
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
Title
Expanded short physical performance battery
Description
Measures lower extremity function
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
Title
Baecke Physical Activity Questionnaire
Description
Self-reported physical activity
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
Title
PROMIS v2.0 Mobility Questionnaire
Description
Self-reported mobility
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
Title
User Experience Questionnaire+
Description
Self-reported hearing device user experience
Time Frame
Measured at time of study enrollment; between 6- and 8-weeks post study enrollment; and at 6-months post study enrollment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
55 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Adults aged 55 to 75 years old with little or no experience with hearing aids
English or Spanish speakers
Exclusion Criteria:
Unable to complete written questionnaires on a tablet without assistance
Refer for cognitive screening score based on criteria using the Mini Mental State Examination
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michelle Arnold, PhD
Phone
8139741262
Email
mlarnold@usf.edu
Facility Information:
Facility Name
University of South Florida
City
Tampa
State/Province
Florida
ZIP/Postal Code
33620
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michelle Arnold, PhD
Phone
813-974-1262
Email
arctlab@usf.edu
First Name & Middle Initial & Last Name & Degree
Sarah Bochat, AuD
Phone
8139741262
Email
arctlab@usf.edu
12. IPD Sharing Statement
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Early Age-Related Hearing Loss Investigation Pilot Study
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