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Telemedicine Referral for Childhood Hearing Loss

N/A
Recruiting
Led By Denise Dillard, PhD
Research Sponsored by University of Arkansas
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up proportion of children who receive follow-up will be measured by the occurrence of an ear/hearing encounter, up to 60 days from the date of screening.
Awards & highlights
No Placebo-Only Group

Summary

This trial will test whether a new telemedicine intervention called STAR can reduce loss to follow-up in rural Alaska after school hearing screenings. It will compare the intervention to the standard referral of a letter home to families, and evaluate over three academic years.

Who is the study for?
This trial is for children in grades K-12 attending participating schools in rural Alaska regions. It aims to address high rates of childhood hearing loss, which is often preventable and related to infections.
What is being tested?
The study compares two methods: the standard referral process versus a telemedicine intervention called STAR, which brings specialty care directly into schools after mobile health screenings.
What are the potential side effects?
Since this trial involves screening and referral processes rather than medical treatments or drugs, there are no direct side effects associated with the interventions being tested.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~proportion of children who receive follow-up will be measured by the occurrence of an ear/hearing encounter, up to 60 days from the date of screening.
This trial's timeline: 3 weeks for screening, Varies for treatment, and proportion of children who receive follow-up will be measured by the occurrence of an ear/hearing encounter, up to 60 days from the date of screening. for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Proportion of children who receive follow-up

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Group I: Standard ReferralExperimental Treatment1 Intervention
Group II: Specialty Telemedicine Access for Referrals (STAR)Experimental Treatment1 Intervention

Find a Location

Who is running the clinical trial?

University of ArkansasLead Sponsor
494 Previous Clinical Trials
144,452 Total Patients Enrolled
Southcentral FoundationOTHER
9 Previous Clinical Trials
1,913 Total Patients Enrolled
Duke UniversityOTHER
2,452 Previous Clinical Trials
2,965,746 Total Patients Enrolled
~3400 spots leftby May 2026