Bridgeport, CTNCT07115030Now EnrollingIRB Ready

Opioid Use Disorder Clinical Trial in Bridgeport, CT

Access cutting-edge opioid use disorder treatment through this clinical trial at a research site in Bridgeport. Study-provided care at no cost to qualified participants.

Sponsored by Yale University

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Expert Care in Bridgeport

Access opioid use disorder specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related opioid use disorder treatment provided free

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Check if you qualify for this opioid use disorder clinical trial in Bridgeport, CT

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Bridgeport

    Convenient for CT residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Bridgeport site if eligible
  4. 4Begin participation

About This Opioid Use Disorder Study in Bridgeport

Using a hybrid type 1 effectiveness-implementation approach, this study aims to evaluate the impact of a novel stepped care model ("PCT+2HOPE") versus treatment as usual (TAU) on increasing retention in community-based medication for opioid use disorder (MOUD) treatment among women who have experienced intimate partner violence (W-IPV). PCT+2HOPE includes Present-Centered Therapy (PCT+) with stepped care as indicated by moderate, severe, or extreme PTSD-related impairment in psychosocial functioning to Helping to Overcome PTSD through Empowerment (HOPE), two evidence-based behavioral interventions adapted for women with opioid use disorder (OUD). We will examine the effectiveness of PCT+2HOPE vs. TAU on the primary outcome (i.e., retention in MOUD treatment) and secondary outcomes related to trauma (i.e., PTSD-related impairment in psychosocial functioning and depression), substance use (i.e. OUD symptom severity, extra-medical opioid use \[i.e., use of prescription opioids without a doctor's prescription; in greater amounts, more often, longer than prescribed, or for a reason other than a doctor said they should be used\], and recovery), and empowerment. We will explore the extent to which the effectiveness of PCT+2HOPE vs. treatment as usual differs based on access to basic needs. We will also conduct an implementation-focused process evaluation.

Sponsor: Yale University

Who Can Participate

Inclusion Criteria

Are ≥ 18 years old;
Receive MOUD treatment at one of the participating sites;
Have received MOUD for \>14 days to allow for initial stabilization;
Have initiated the current treatment episode within the past 12 months;
Experienced physical or psychological IPV in their lifetime;
Have at least moderate impairment in psychosocial functioning (on B-IPF) as a result of PTSD symptoms;
Available during the date/time of the intervention group
Able to read/understand English; and
Provide written informed consent.

Exclusion Criteria

Fail a capacity-to-consent questionnaire;
Have an unstable medical condition (e.g., hospitalization, planned surgery, newly starting chemotherapy, plans for palliative care) and/or unstable psychiatric illness (e.g., untreated psychosis) that would interfere with their ability to participate in study activities;
Will be unavailable for \>4 consecutive weeks during the study period (e.g., anticipated move, planned surgery);
Are unable to read/understand English;
Inability to provide at least one form of contact

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Bridgeport?

Yes, this clinical trial (NCT07115030) has an active research site in Bridgeport, CT that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Opioid Use Disorder Treatment Options in Bridgeport, CT

If you're searching for opioid use disorder treatment options in Bridgeport, CT, this clinical trial (NCT07115030) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Bridgeport research site is actively enrolling participants for this clinical trial. You'll receive care from experienced opioid use disorder specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all opioid use disorder clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Bridgeport, CT