Ignite Creation Date:
2024-05-06 @ 6:35 PM
Last Modification Date:
2024-10-26 @ 2:50 PM
Study NCT ID:
NCT05711537
Status:
COMPLETED
Last Update Posted:
2024-06-25
First Post:
2023-01-25
Brief Title:
Auricular Acupressure as a Non-Opioid Adjuvant in Opioid Tolerant Patients
Sponsor:
Wake Forest University Health Sciences
Organization:
Wake Forest University Health Sciences
Study Overview
Official Title:
Auricular Acupressure as a Non-Opioid Adjuvant in Opioid Tolerant Patients
Status:
COMPLETED
Status Verified Date:
2024-06
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 purpose of this study is to determine if the addition of auricular acupressure to the typical pharmacological regimen given to patients on the chronic painaddiction service will lower pain scores and decrease pain medication usage
Detailed Description:
Participants will be asked to complete baseline questionnaires After completion a study interventionist will place 10 adhesive acupressure padsseeds on the participants ears 5 acupressure pads per ear The pads will be placed on specific sites of the ear that are thought to help with pain and overall well-being Over the course of 3 days participants will be asked to apply a small amount of pressure with their finger to each of the pads and answer study questionnaires
This feasibility trial is being performed in collaboration with the Battlefield Auricular Acupressure BAApress Training and Intervention Fidelity study IRB00084011
This feasibility trial is being performed in collaboration with the Battlefield Auricular Acupressure BAApress Training and Intervention Fidelity study IRB00084011
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
True
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?:
None