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Not yet recruitingNCT06943976Updated Apr 25, 2025

How Parents, Children, and Clinicians Experience Digital Health Tools in Pediatric Audiology

An observational study in Hearing Loss, Bilateral or Unilateral, sponsored by Erasmus Medical Center. Not yet recruiting. Open to participants aged 7 Years to 90 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-04-25.

Sponsored by Erasmus Medical Center · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
80
Ages
7 Years to 90 Years
Sex
All
01

Study summary

The goal of this observational study is to understand how children with hearing loss, their parents, and health care providers experience digital health questionnaires that are completed before audiology follow-up appointments. The study focuses on children and adolescents (aged 7-18 years old) with hearing loss, and their parents, visiting the Audiology outpatient clinic of the Erasmus MC Sophia Children's Hospital.

The main questions it aims to answer are:

  • How do parents, children, and clinicians experience digital questionnaires like the HEAR-QL before an audiology visit?
  • Do these digital tools help improve communication and preparation for the appointment?

Participants will:

  • Be invited to complete a short feedback questionnaire about their experience with digital tools
  • Share their views on how helpful or relevant the questionnaires were
  • Health care providers will also give feedback on how they use and interpret the responses in clinical care
Read the detailed description

This observational study evaluates the experiences of children with hearing loss, their parents or caregivers, and audiology health care providers with digital health questionnaires that are completed before pediatric audiology follow-up visits. The study is conducted at the Audiology outpatient clinic of the Erasmus MC Sophia Children's Hospital in Rotterdam, the Netherlands.

As part of routine clinical care, families receive electronic patient-reported outcome measures (PROMs) prior to their appointment, including the Dutch versions of the HEAR-QL questionnaire. These questionnaires are designed to gather insights into the child's hearing-related quality of life and relevant experiences related to hearing care.

Participants in this study include children and adolescents (ages 7-18 years) with unilateral or bilateral hearing loss, their caregivers, and health care professionals (audiologists, speech language pathologists and/or ENT specialists). All participants are invited to provide feedback on the digital questionnaires via brief evaluation surveys (PREMs). This information is collected anonymously and used to understand the usability, relevance, and clinical value of the tools from both the patient and provider perspectives.

Registry-related procedures and quality factors:

  • Quality assurance plan: All data are collected using a secure digital platform. Data entry is automated via survey completion, reducing the risk of manual input errors. Registry procedures follow institutional data management standards.
  • Data checks and validation: Built-in logic and range checks are applied within the digital survey software to prevent incomplete or inconsistent responses.
  • Source data verification: No source data verification is applied, as this study does not use patient medical records beyond the standard demographic and audiological information collected with informed consent.
  • Data dictionary: A standardized variable list is maintained, including definitions, coding schemes, and units of measurement. The HEAR-QL scoring methodology is applied as per published validation guidelines.
  • Standard Operating Procedures (SOPs): SOPs exist for patient approach, informed consent, survey distribution, data storage, and privacy protection. All procedures align with institutional review board approvals.
  • Sample size: The study aims to include a minimum of 50 families (about 80 respondents) over a 4-month period, which is sufficient for descriptive and exploratory analyses of user experience outcomes.
  • Missing data: Missing data is not expected, as all questions in the digital questionnaires are required fields. The system prevents submission of incomplete surveys. Therefore, no item-level missingness or imputation procedures are applicable.
  • Statistical analysis plan: Quantitative survey responses will be summarized using descriptive statistics (e.g., means, medians, proportions). Associations between user experience scores and patient characteristics (e.g., age, hearing device type) may be explored using nonparametric tests or regression analyses as appropriate. Qualitative comments from participants will be grouped thematically.

This study aims to contribute to the growing body of knowledge on patient and provider experiences with digital health tools in pediatric audiology. Results may inform future implementation and optimization of PROMs in routine hearing care.

02

Conditions studied

  • Hearing Loss, Bilateral or Unilateral

Keywords

  • Hearing Loss
  • Quality of Life
  • PROMs
  • PREMs
  • Children
  • Digital Health Care
03

Who can participate

Ages eligible
7 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Participants will be selected from the population of children and adolescents aged 7 to 18 years with unilateral or bilateral hearing loss who attend the Audiology outpatient clinic of Erasmus MC Sophia Children's Hospital in Rotterdam, the Netherlands. Their parents or primary caregivers will also be invited to participate. Additionally, audiologists and other health care professionals working at the same clinic and using patient-reported outcome measures (PROMs) in routine care will be included in the study.

Inclusion criteria

  • Children and adolescents, aged 7-18 years old, with rehabilitated unilateral or bilateral hearing loss, attending the Audiology outpatient clinic of the Erasmus MC Sophia Children's Hospital in Rotterdam, the Netherlands
  • The corresponding parents or caregivers of these pediatric patients
  • Audiologists or other health care providers who systematically use the PROMs during patient interactions at the same Audiology outpatient clinic.

Exclusion criteria

Exclusion Criteria:

  • Children or adolescents who are unable to complete the questionnaire, even with support in reading and understanding the items provided by their parents or caregivers.
04

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
80 participants (estimated)
Patient registry
No
05

What researchers measure

Primary outcomes

  1. Experience with digital health questionnaires

    Experience scores from a custom feedback survey completed by parents/caregivers and children aged 7-18 years, evaluating clarity, relevance, and burden of digital questionnaires.

    Time frame: Within 3 months after the audiology appointment

Secondary outcomes

  1. Clinician-perceived utility of digital questionnaires

    Ratings from audiology/health care staff on the usefulness of digital patient-reported outcome measures (PROMs) in preparing for or guiding the consultation.

    Time frame: Within the time frame of the patient enrollment

06

Study locations

No study locations are listed for this record.

07

Registry details

Key details

Study ID
NCT06943976
Lead sponsor
Erasmus Medical Center
Responsible party
Christina Batthyany (Resident and PhD Candidate in Otorhinolaryngology - Head and Neck Surgery, Erasmus Medical Center) — Principal investigator
First posted
Apr 25, 2025
Start date
May 1, 2025 (estimated)
Primary completion
Aug 1, 2025 (estimated)
Completion
Sep 1, 2025 (estimated)
Last update
Apr 25, 2025

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2025. You cannot join it, but the record below documents what was studied.

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