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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05030961
Other study ID # 20210584
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 1, 2021
Est. completion date June 1, 2023

Study information

Verified date June 2023
Source University of Miami
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to see if remote visits for pediatric cochlear implant patients are possible. The investigator will be assessing whether a multi-disciplinary team approach can be achieved remotely for patients both undergoing the cochlear implant (CI) process and for those who have already been implanted.


Recruitment information / eligibility

Status Completed
Enrollment 86
Est. completion date June 1, 2023
Est. primary completion date June 1, 2023
Accepts healthy volunteers No
Gender All
Age group 0 Years to 12 Years
Eligibility Inclusion Criteria: New patients undergoing CI evaluation: 1. English speaking patients (parents can speak English and/or Spanish) 2. Ages 0-12 years who are cochlear implant candidates and undergoing the evaluation process Established CI recipients: 1. English speaking patients (parents can speak English and/or Spanish) 2. Ages 1-12 with at least 6 months of CI experience with a company that has remote programming capacity Exclusion Criteria: 1. Patients with families who speak languages other than English or Spanish 2. Patients who do not live in Florida 3. Patients who have any condition that, in the opinion of the investigator, would compromise the well-being of the patient or the study or prevent the patient from meeting or performing study requirements

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Virtual team-based clinic
Virtual team-based clinic will include consultation, counseling, and education from pediatric audiology, psychology, auditory verbal therapy, and education. Each session lasts approximately 30 minutes with a total of 3 sessions within the year.
Remote cochlear implant programming
Remote cochlear implant programming will be provided via Zoom on a study-provided encrypted laptop.

Locations

Country Name City State
United States University of Miami Miami Florida

Sponsors (2)

Lead Sponsor Collaborator
University of Miami Stanley J. Glaser Foundation

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Electrode Impedances Electrode Impedances values, reported in kOhm, will be extracted from the cochlear implant software Up to 1 year
Primary Electrically evoked compound potential values Electrically evoked compound potential values, reported in mV, will be extracted from the cochlear implant software Up to 1 year
Primary Datalogging Datalogging, reported in hours per week, will be extracted from the cochlear implant software Up to 1 year
Primary Threshold/Upper stimulation levels As measured from the cochlear implant software Up to 1 year
Primary LittleEars questionnaire scores The LittleEars auditory questionnaire (LEAQ) uses parent responses to assess auditory behavior in children up to 24 months of age. The questionnaire is scored from 0 to 35 with 0 indicating poorer performance and 35 indicating better performance. Up to 1 year
Primary Auditory Skills Checklist (ASC) scores ASC has a Total Score ranges from zero to 70, with higher scores indicating development of increasingly complex listening skills Up to 1 year
Secondary Behavior Assessment System for Children version 3 (BASC-3) scores BASC-3 is scored 0-120 as a T score. Any scores between 60-70 is considered at risk / requires monitoring and scores greater than 70 are considered clinically significant / an area that likely requires therapeutic intervention. Up to 1 year
Secondary Patient Health Questionnaire version 8 (PHQ-8) scores PHQ-8 has 8 items rated on a scale from "not at all" (0) to "nearly every day" (3), with higher scores indicating greater frequency of depressive symptoms. The sum of the items indicates the overall level of depressive symptoms indicating mild (5-9), moderate (10-14), moderately severe (15-19), and severe depressive symptoms (20- 24). Up to 1 year
Secondary Generalized Anxiety Disorder version 7 (GAD-7) scores GAD-7 is a 7-item self-report questionnaire of anxiety symptomatology in the past 14 days. Respondents rate the frequency of each item during the past two weeks on a 0-3-point scale ranging from not at all (0) to nearly every day (3). The sum of the items indicates the overall level of anxiety symptoms indicating mild (0-4), moderate (5-9), moderately severe (10-14), and severe (15- 21). Up to 1 year
Secondary Quality of Life- CI (QoL-CI) scores QoL-CI is scored 0-100 with higher scores indicating better quality of life. Up to 1 year
Secondary Cochlear Implant Quality of Life-35 Profile (CIQOL-35 Profile) scores CIQOL-35 Profile is a 35 item questionnaire with a total score ranging from 0-100% with a higher score indicating a higher level of functional ability with a cochlear implant Up to 1 year
Secondary Parenting Stress Index/Short Form (PSI) scores Parenting Stress Index/Short Form (PSI) contains 36 items rated on a 6-point Likert scale (1 = Strongly Disagree to 5 = Strongly Agree) and a total score. Higher scores indicate increased parenting stress. Up to 1 year
Secondary Parenting Stress-CI scores Parenting Stress-CI is completed by the parent and scored from "not at all stressful" (0) to "very stressful" (3) with higher scores indicating greater degrees of parenting stress. For parents of children 0-5 years, there are 15 items. For parents of children 6-12 years there are 8 items. Up to 1 year
Secondary Scale of Parental Involvement and Self-Efficacy-Revised (SPISE-R) scores The SPISE-R is comprised of 46 questions that uses a 7-point Likert scale to query parents' beliefs, knowledge, confidence, and actions relevant to supporting their child's auditory access and spoken language development. The total average score will range from 1 to 7 with 7 indicating the highest score / highest level of parental involvement and self efficacy. Up to 1 year
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