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EPPIC: Easing Pelvic Pain Interventions Clinical Research Program

Study acronym: EPPIC
StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Interventions: Minimal Contact-Cognitive Behavior Therapy (Behavioral), Patient Education/Support (Behavioral) to Minimal Contact-Cognitive Behavior Therapy (Behavioral), Patient Education/Support (Behavioral) Show 5 more changesShow less
    • Eligibility criteria expanded, about 28 words
    • Secondary endpoints: 6 to 7
    • Study description revised
    • Site contacts updated at 1 of 3 sites
    • Publications: details revised at 3 of 3 entries
  2. Primary completion date: Nov 30, 2025 to Feb 2028
    • Study completion date: May 31, 2026 to Jul 31, 2028
    v11
  3. Site contacts updated at 1 of 3 sitesv10
  4. 2 versions Re-verified since Oct 11, 2023, no change to tracked fieldsv8-v9
  5. Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Jul 15, 2022 to Aug 10, 2022
    • Site details revised at 3 of 3 sites
    • Collaborators: 3 to 2
    v7
Show 5 earlier versionsHide 5 earlier versions
  1. Re-verified, no change to tracked fieldsv6
  2. Primary completion date: Oct 2026 to Nov 30, 2025
    • Study completion date: Oct 2026 to May 31, 2026
    • Start date: Jul 11, 2022 to Jul 15, 2022
    v5
  3. Phase: Phase 2/3 to Not applicable
    • Start date: May 1, 2022 to Jul 11, 2022
    v4
  4. Eligibility criteria revised
    • Study sites revised (3)
    v3
  5. Start date: Jan 1, 2022 to May 1, 2022v2
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT05127616
Lead Sponsor State University of New York at Buffalo
Collaborators: University of California, Los Angeles, University of Michigan
Conditions
(from sponsor)		 Urologic Chronic Pelvic Pain Syndrome (UCPPS), Interstitial Cystitis, Bladder Pain Syndrome, Chronic Prostatitis, Chronic Pain, Chronic Pelvic Pain Syndrome, Chronic Overlapping Pain Disorders
Related terms Chronic Pain, Cystitis, Interstitial
Enrollment 240 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov