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EPPIC: Easing Pelvic Pain Interventions Clinical Research Program
NCT05127616 · View on ClinicalTrials.gov ↗
Study Summary
The EPPIC (Easing Pelvic Pain Interventions Clinical Research Program) study evaluates an ultra-brief, 4 session cognitive behavioral pain treatment transdiagnostic in design for urologic chronic pain syndrome (UCPPS) with clinical and practical advantages over existing behavioral therapies whose length and focus limits their adoption by clinicians and coverage for mechanistically similar comorbidities. A theoretically informed, practical, empirically grounded approach will systematically unpack CBT's working mechanisms, clarify for whom it works, ease dissemination, appeal to patients, providers, payers, and policy makers in the COVID-19 era favoring low resource intensity treatments, and reduce cost and inefficiencies associated with high intensity therapies whose complexity, length, and scarcity restricts uptake and impact.
Conditions Studied
Interventions
- BEHAVIORAL Minimal Contact-Cognitive Behavior Therapy
- BEHAVIORAL Patient Education/Support
Study Locations (3)
California
- UCLA — Los Angeles
Michigan
- University of Michigan — Ann Arbor
New York
- University at Buffalo (the only clinical site where treatment is delivered) — Buffalo
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 240 participants |
| Start Date | 2022-08-10 |
| Est. Completion | 2028-07-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05127616
The ClinicalTrials.gov registry entry for NCT05127616 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 240 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is State University of New York at Buffalo, which has 234 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 7 conditions, with Chronic Pain appearing as the primary indexed condition, and to 2 interventions — of which Minimal Contact-Cognitive Behavior Therapy is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05127616 reports 3 study locations spanning 3 distinct geographic areas — top geographies include California, Michigan, New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05127616 about?
NCT05127616 is a clinical study titled "EPPIC: Easing Pelvic Pain Interventions Clinical Research Program". The EPPIC (Easing Pelvic Pain Interventions Clinical Research Program) study evaluates an ultra-brief, 4 session cognitive behavioral pain treatment transdiagnostic in design for urologic chronic pain syndrome (UCPPS) with clinical and practical advantages over existing behavioral therapies whose le...
What is the current status of trial NCT05127616?
This trial is currently recruiting. It is a NA study. The enrollment target is 240 participants. The study started on 2022-08-10. Estimated completion is 2028-07-31.
What conditions does trial NCT05127616 study?
This clinical trial studies the following conditions: Chronic Pain, Interstitial Cystitis, Bladder Pain Syndrome, Chronic Pelvic Pain Syndrome, Chronic Prostatitis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05127616?
The interventions under investigation include: Minimal Contact-Cognitive Behavior Therapy (BEHAVIORAL), Patient Education/Support (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05127616?
This trial is sponsored by State University of New York at Buffalo, which has 234 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05127616 being conducted?
This trial has 3 study locations across California, Michigan, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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