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NCT04988061 Clinical Trial

Proactive Counselling Towards Follow-ups in Newborn Hearing Screening

Hearing Loss Clinical Trial

Official title:
Result of Proactive Parental Educating and Counselling Towards Follow-ups in Parents Whose Infant Fail Newborn Hearing Screening

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT04988061
Other study ID # 64-220-13-1
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date August 20, 2021
Est. completion date January 31, 2024

Study information
Verified date September 2022
Source Prince of Songkla University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study aims to investigate if proactive parental educating and counselling can minimize loss to follow-ups of parents whose infant fail newborn hearing screening.

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date January 31, 2024
Est. primary completion date July 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - The parents whose infants do not pass hearing screening Exclusion Criteria: - The parents whose infants have illnesses and are not ready for hearing screening - The parents who decide to migrate to other areas

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• counselling
Educating and Counselling with personal communication for 10-15 minutes and written information about the importance of early identification and intervention for hearing loss are provided by a physician. Also, the information about hearing screening results and an appointment date are provided by a physician.

Locations
Country Name City State
Thailand Faculty of Medicine, Prince of Songkla University Hat Yai Songkhla

Sponsors (1)
Lead Sponsor Collaborator
Prince of Songkla University

Country where clinical trial is conducted

Thailand, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of participants with loss to follow-ups in all participants whose infants require follow-ups A loss to follow-up rate which is calculated from number of participants with loss to follow-ups divided by number of all participants whose infants require follow-ups 6 months
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