Ignite Creation Date:
2024-05-06 @ 3:55 PM
Last Modification Date:
2024-10-26 @ 1:59 PM
Study NCT ID:
NCT04803045
Status:
COMPLETED
Last Update Posted:
2021-03-22
First Post:
2021-03-15
Brief Title:
Does a Brief Intervention Decrease Patient Drop Out Rates
Sponsor:
Boston IVF
Organization:
Boston IVF
Study Overview
Official Title:
The Impact of a Brief Intervention on Retention Rates With Patients Who Did Not Return to Care After an Initial Physician Visit
Status:
COMPLETED
Status Verified Date:
2021-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this study is to determine a if a follow-up email to selected patients who had an initial consult with an infertility specialist but did not return for a second visit would change return to care behavior and b why patients had not returned
Detailed Description:
From July 2017 to March 2018 all patients who had attended an initial visit with an infertility specialist at the clinic but had not returned for at least three months were selected to receive a follow up email Those selected for an email excluded patients who the Investigators knew had achieved a pregnancy already had a plan for treatment had visited for an egg freeze and all LGTBQ patients The email asked if the patient had any questions about that visit offered support to the patient and included contact information for the patient liaison sending the email The email also asked each participant to indicate why they had not returned and were provided 4 options and an opportunity to write in a response From April 2018 to December 2018 no emails were sent to patients No other change of patient contact practice was initiated during the trial period This study will observe routine to care behavior of these patients after 11 months post initial consult date
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None