Your session is about to expire
← Back to Search
Patient Education for Pain Management
N/A
Waitlist Available
Led By Anping Xie, PhD
Research Sponsored by Johns Hopkins University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up time of each participant's standard of care clinic visit, up to 1 year from enrollment
Awards & highlights
Study Summary
This trial will evaluate an educational intervention to improve patient engagement in perioperative pain management, compared to usual care.
Who is the study for?
This trial is for patients at Johns Hopkins Personalized Pain Program Clinic dealing with opioid use and postoperative pain. It's not suitable for individuals who have thoughts of suicide, a primary psychotic disorder, or those who cannot speak English.Check my eligibility
What is being tested?
The study tests an educational intervention designed to improve patient engagement in managing pain after surgery. Participants are randomly placed into groups to either receive the new Patient Engagement Tools and Educational Guide or continue with standard care.See study design
What are the potential side effects?
Since this trial involves educational tools rather than medications, traditional side effects like you'd see with drugs aren't expected. However, participants may experience varying levels of stress or anxiety related to engaging more actively in their pain management.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ time of each participant's standard of care clinic visit, up to 1 year from enrollment
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~time of each participant's standard of care clinic visit, up to 1 year from enrollment
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Patient engagement as assessed by a patient engagement survey
Secondary outcome measures
Functional status as assessed by the 36-Item Short Form Health Survey
Functional status as assessed by the Insomnia Severity Index
Opioid consumption as assessed by daily morphine milligram equivalents
+3 moreTrial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Cohort A - Patient Engagement ToolsExperimental Treatment1 Intervention
Participants will be enrolled from the a pain management clinic. Participants randomized into the experimental cohort will receive access to a clinic brochure, clinic website, as well as 'My Pain Passport' and 'My Treatment Plan' tools.
Group II: Cohort B - Educational GuidePlacebo Group1 Intervention
Participants randomized into the control cohort will receive a brief educational guide on general pain management.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Patient Engagement Tools
2022
N/A
~180
Find a Location
Who is running the clinical trial?
Johns Hopkins UniversityLead Sponsor
2,260 Previous Clinical Trials
14,820,602 Total Patients Enrolled
5 Trials studying Postoperative Pain
177 Patients Enrolled for Postoperative Pain
Centers for Disease Control and PreventionFED
875 Previous Clinical Trials
22,477,224 Total Patients Enrolled
Anping Xie, PhDPrincipal InvestigatorJohns Hopkins University
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have a serious mental illness that affects your thinking and perception.All patients at the Johns Hopkins Personalized Pain Program Clinic are excluded from the study.I do not have thoughts of harming myself at the moment.I do not speak English.
Research Study Groups:
This trial has the following groups:- Group 1: Cohort B - Educational Guide
- Group 2: Cohort A - Patient Engagement Tools
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there any unfilled positions in this clinical trial?
"According to the clinicaltrials.gov registry, this experiment is currently enrolling volunteers and was first made available on February 1st 2022 before receiving its most recent update two weeks later."
Answered by AI
What is the current size of the cohort participating in this research project?
"Affirmative. According to clinicaltrials.gov, this medical research project is currently seeking volunteers for participation; the protocol was posted on February 1st 2022 and revised on Valentine's Day of that same year. 200 participants are expected from one site."
Answered by AI
Share this study with friends
Copy Link
Messenger