Viewing Study NCT06604559



Ignite Creation Date: 2024-10-26 @ 3:40 PM
Last Modification Date: 2024-10-26 @ 3:40 PM
Study NCT ID: NCT06604559
Status: RECRUITING
Last Update Posted: None
First Post: 2024-08-11

Brief Title: The Effect of Patient Discharge From the Maternal and Fetal Medicine Unit With Receiving a Discharge Letter Later Using the Apollo App on Discharge Data Safety and Patient Satisfaction
Sponsor: None
Organization: None

Study Overview

Official Title: The Effect of Patient Discharge From the Maternal and Fetal Medicine Unit With Receiving a Discharge Letter Later Using the Apollo App on Discharge Data Safety and Patient Satisfaction - a Prospective Randomized Controlled Trial
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: Women admitted to the maternal and fetal medicine unit are often discharged after a short hospital stay The routine work in the department is prioritized such that the discharge letter are written In the last year the Apollo mobile application app was introduced It contains general information on the medical center and the maternal and fetal unit department as well as the medical records laboratory results and summary and discharge letters The Apollo app is used in the maternal and fetal unit in the discharge process so the patient can receive the discharge letter in the app and does not need to wait until the discharge letter is written

It is not known whether this process is more effective than the regular discharge process and patients satisfaction was not assessed previously

In the present study we will compare discharge data satisfaction and safety of discharging using the Apollo app versus the routine process
Detailed Description: None

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