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NCT05658926 Clinical Trial

A Brief Intervention for Patients on Opioids for Acute Pain

Acute Pain Clinical Trial

Official title:
A Brief Intervention for Patients on Opioids for Acute Pain

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05658926
Other study ID # HFHS Acute Pain
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2017
Est. completion date April 30, 2018

Study information
Verified date December 2022
Source Henry Ford Health System
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to evaluate benefits of a brief intervention for patients who are prescribed opioids for acute pain.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date April 30, 2018
Est. primary completion date March 31, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients who are admitted to Henry Ford Hospital - Patients who have been evaluated by the Psychosomatic Medicine Service - Patients who are prescribed at least one opioid for an acute pain condition Exclusion Criteria: - Patients taking an opioid for a chronic pain condition within the previous year - History of an opioid use disorder.

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Mindfulness
Patients will learn how to use diaphragmatic breathing with mindfulness
Other:
• Education
Patients will be provided with education regarding the Gate Control Theory of Pain.

Locations
Country Name City State
United States Henry Ford Health System Detroit Michigan

Sponsors (1)
Lead Sponsor Collaborator
Henry Ford Health System

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain severity Pain severity rated on a 0-10 scale Change from pre- to post-intervention. The intervention is approximately 10 minutes so the measurements are taken about 10 minutes apart.
Secondary Stress level Stress level rated on a 0-10 scale Change from pre- to post-intervention. The intervention is approximately 10 minutes so the measurements are taken about 10 minutes apart
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