Viewing Study NCT06640023



Ignite Creation Date: 2024-10-26 @ 3:42 PM
Last Modification Date: 2024-10-26 @ 3:42 PM
Study NCT ID: NCT06640023
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-09-30

Brief Title: The Study in Outpatient Medicine Using Nudges to Improve Sleep
Sponsor: None
Organization: None

Study Overview

Official Title: The Study in Outpatient Medicine Using Nudges to Improve Sleep the SOMNUS Trial
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-10
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: SOMNUS
Brief Summary: The goal of this clinical trial is to learn if electronic health record EHR nudges changes to the EHR that do not restrict freedom of choice or alter incentives can reduce Z-drug prescribing in primary care clinics for patients with insomnia The main questions it aims to answer are

1 Can Z-drug prescribing be reduced by setting the dispense quantity default of new Z-drug orders in the EHR to 10 pills with 0 refills
2 Can Z-drug prescribing be reduced by an EHR alert that suggests clinicians remove a Z-drug andor add an evidence-based behavioral treatment for insomnia followed by a request to justify their reasoning if the suggestion is not followed
3 Does combining these two nudges reduce Z-drug prescribing

Researchers will compare each nudge individually and in combination to an guideline education control group to see if each nudge separately and in combination can reduce Z-drug prescribing

Clinician-participants will

1 Complete an introductory educational module about treating insomnia and relevant EHR changes
2 Complete their routine patient visits
3 Either experience EHR changes when prescribing Z-drugs including a Z-drug dispense quantity default of 10 pills for new orders a prompt to remove or justify Z-drug orders both or neither
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