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Collaborative Care for Opioid Addiction and Mental Health (CHAMP Trial)
CHAMP Trial Summary
This trial is testing if a Collaborative Care model can treat opioid use disorder and mental health disorders together in primary care.
CHAMP Trial Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.CHAMP Trial Design
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Who is running the clinical trial?
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- Group 1: Collaborative Care for Mental Health Disorders
- Group 2: Collaborative Care for Opioid Use Disorder
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- 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
In how many locations can this medical experiment be conducted?
"The trial is currently being undertaken at 27 different sites, including Dunwoody, Stone Mountain and Coeur d'Alene. To reduce travel burdens for participants, it's important to select a location close to them when enrolling in the study."
Is there availability for participants in this research endeavor?
"Affirmative. Clinicaltrials.gov has data that confirms this medical trial is currently recruiting participants, first posted on November 20th 2020 and edited as recently as June 5th 2021. They are seeking a total of 1200 patients from 27 different clinical sites."
How many participants have enrolled in this research project?
"To successfully complete this medical trial, 1200 qualifying individuals need to join. Potential participants can do so at the Emory Clinic in Saint Joseph's - Primary Care (Dunwoody, Idaho) or at Emory at Dunwoody - Family Medicine (Stone Mountain, Illinois)."
What is the main purpose of this clinical trial?
"This 6-month clinical trial will measure the Change in Mental health Functioning as its primary outcome. Additionally, it will assess Change in Anxiety Symptoms (using the PROMIS Measure - Emotional Distress, Anxiety, Short Form 7a), Change in PTSD Symptoms (utilizing PCL-5 score range 0-80) and Opioid Use Disorder Medication Persistence (defined by a ratio of days taking medication to total number of prescribed days)."
Who else is applying?
What site did they apply to?
What portion of applicants met pre-screening criteria?
Why did patients apply to this trial?
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