Long-term Recovery in OUD

  • STATUS
    Recruiting
Updated on 19 February 2024

Summary

The goals of this project are: 1) Establish normative data on long-term recovery course of OUD across patients, community supports, and providers and 2) Quantify the impact of MAT on long-term recovery from OUD.

Description

Opioid Use Disorder (OUD) is a life-long disorder; however, most research and treatment use short-term approaches and follow-up. Medication-Assisted Treatment (MAT) is successful for short-term recovery from OUD, which has improved survival rates. This has resulted in a critical need to know how best to support individuals in long-term OUD recovery.

Meeting these goals will reduce OUD overdose and incidence by 1) Developing a comprehensive guide to best practices for MAT in long-term OUD recovery; 2) Characterizing normative data on recovery course(s) that can guide appropriate recovery expectations and reduce stigma; and 3) Providing proof of concept to strengthen subsequent federal funding applications studying long-term OUD recovery.

Details
Condition Opioid Use Disorder
Age 18years - 100years
Clinical Study IdentifierTX10209
Last Modified on19 February 2024

Eligibility

How to participate?

Step 1 Connect with a study center
Message sent successfully.
We have submitted the information you provided to the research team at the location you chose. For your records, we have sent a copy of the message to your email address.
If you would like to be informed of other studies that may be of interest to you, you may sign up for Patient Notification Service.
Sign up

Send a message

Enter your contact details to connect with study team


Email

View email

Phone

Phone country flag

View phone
Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Preferred way of contact label
Race
Ethnicity
Other language

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.