Viewing Study NCT06543784



Ignite Creation Date: 2024-10-25 @ 8:01 PM
Last Modification Date: 2024-10-26 @ 3:37 PM
Study NCT ID: NCT06543784
Status: RECRUITING
Last Update Posted: None
First Post: 2024-07-30

Brief Title: Preconception Carrier Screening at the Erasmus MC
Sponsor: None
Organization: None

Study Overview

Official Title: The New Wave of Preconception Carrier Screening the Nurse Practitioner in the Lead
Status: RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Rationale A recent advisory report by the Health Council has recommended that all prospective parents should have the opportunity to undergo preconception carrier screening Consequentlythere will no longer be any prerequisites for referring a couple It is expected that there will be an increase in the number of prospective parents seeking counseling for preconception carrier screening This is anticipated to result in an increase in the number of referrals leading to several points of attention

Objectives The aim of the research is to gather insights perspectives and experiences from healthcare professionals and prospective parents in order to design a care pathway for offering preconception carrier screening at Erasmus MC and the Rotterdam region This will also include examining the role that nurse practitioners can play in this offering
Detailed Description: Study type Exploratory research Study population Healthcare professionals involved in preconception carrier screening and potential prospective parents who might want to undergo preconception carrier screening in the future Methods Semi-structured interviews and focus groups will be used to explore topics which will be audio recorded and transcribed verbatim The results will be analyzed by two to three researchers independently following the principles of grounded theory

Burden and risks There are no risks associated with this research For the interviewees and participants of the focus groups there is the burden of time investment Recruitment and consent Health care professionals and potential prospective parents will be asked for participation in the study by the treating physician If they consent to be approached they will be informed about the study and contacted by the researcher If willing to participate an appointment for the interviewfocus group is scheduled Before the start of the interviewfocus group signed informed consent will be obtained

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None