EPPIC: Easing Pelvic Pain Interventions Clinical Research Program

Chronic Pain Clinical Trial

— EPPIC  

Official title:

A Brief, Transdiagnostic Cognitive Behavioral Treatment for Urological Chronic Pelvic Pain Syndrome: Processes, Predictions, Outcomes

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05127616
• Other study ID #: STUDY00005691
• Secondary ID: NIH Grant/1R01DK
• Status: Recruiting
• Phase: N/A
• Start date: August 10, 2022
• Est. completion date: May 31, 2026

Study information

• Verified date: October 2023
• Source: State University of New York at Buffalo
• Contact: Jeffrey Lackner, PsyD
• Phone: 716-898-5671
• Email: lackner[@]buffalo.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Description:

Urologic chronic pelvic pain syndrome (UCPPS) encompasses several common, costly diagnoses including interstitial cystitis/bladder pain syndrome and chronic prostatitis/chronic pelvic pain syndrome that are poorly understood and inadequately treated. Their prolonged personal and economic costs are amplified by the frequent co-occurrence of a cluster of centralized pain conditions (particularly irritable bowel syndrome 3 [IBS]) but also fibromyalgia [FMS], chronic headache, chronic fatigue, etc.) called Chronic Overlapping Pain Conditions (COPC). Clinically, the notion that these syndromes share a centralized pain phenotype with a fundamental disturbance in pain or sensory processing dovetails with our preliminary research showing that a novel transdiagnostic behavioral treatment emphasizing a single common mechanistic pathway (i.e. inflexible cognitive style) reduces severity of both targeted (IBS) and untargeted multisymptom COPCs that include (but is not limited to) to UCPPS, FMS, chronic fatigue, and chronic headache. If effective in a larger scale study, a transdiagnostic UCPPS treatment would offer a more efficient, accessible, and broadly useful strategy for improving chronic pelvic pain and its most frequent and complicating comorbidities. To this end, the investigators will randomize 240 UCPPS subjects (18-70 yrs.) of any gender and race to a 4-session version of CBT that teaches skills for self-managing UCPPS symptoms (e.g. pelvic pain, urinary symptoms such as urinary frequency, urgency) with minimal clinician oversight (MC-CBT) or a four-session non-specific education/support control (EDU). Efficacy assessments will be administered at pre-treatment baseline and two weeks after the end of the 10-week acute phase using the patient version of the Clinical Global Impressions Scale and validated with the physician version rated by MD assessors blind to treatment assignment. The investigators hypothesize MC-CBT will deliver significantly greater UCPPS symptom improvement than EDU (Aim 1). Additional aims include characterizing the durability of effects 3- and 6 months post treatment (Aim 2). To increase the efficacy and efficiency of behavioral pain treatments, the investigators draw upon Beck's transdiagnostic cognitive model to characterize the precise cognitive procedures and corresponding operative processes (e.g., cognitive distancing, context sensitivity, coping flexibility, repetitive negative thought) that drive MC-CBT induced UCPPS symptom relief relative to EDU (Aim 3) as well as baseline patient variables that moderate differential response (Aim 3) with the ultimate goal of more proactive patient-treatment matching fundamental to the goals of personalized medicine. By applying innovative statistical modelling (e.g. dominance analysis, Randomized Explanatory Trial analyses) to study aims in the context of a rigorously designed behavioral trial, the researchers expand the portfolio of nondrug pain treatments for UCPPS and co-aggregating COPCs to include one whose brevity, convenience, and transdiagnostic design "meets patients where they are" and addresses the practical (access, complexity, cost), clinical (breadth, durability, magnitude of effects, patient preference) and conceptual (untargeted comorbidities, non-pain somatic symptoms) challenges that have impeded uptake and public health impact of evidence-based behavioral pain treatments at a time when our most vulnerable high impact pain patients are in greatest need.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 240
• Est. completion date: May 31, 2026
• Est. primary completion date: November 30, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Ages 18-70 years (inclusive)

• Male or female

• All genders, races, ethnic groups

• MD-confirmed diagnosis of IC/BPS or CP/CPPS by study urologist or urogynecologist

• Pelvic pain including uncomfortable sensations of pressure or discomfort that are not described as outright pain) of at least six months duration

• Pelvic pain intensity of at least moderate severity (defined as 3 or greater on a 0-10 Numerical Rating Scale and causes life interference weekly and limit(s) participant's life or work-related activities, general activity level, and/or enjoyment of life) over the past 3 months.

• Ability to understand and provide informed consent

• Either not taking medications or if taking medications willing to refrain from starting new medications until after the initial 2-week pre-treatment baseline period ends unless medically necessary.

• A minimum 6th grade reading level based on the Wide Range Achievement Test (WRAT 4)

• Willing to be randomized to either CBT or Support/Education and to follow the protocol to which s/he has been assigned

• Willing to be contacted for follow up assessments at week 12 and 3, 6 months after treatment ends

• Willing to attend sessions

• Able to maintain symptom diaries and complete paper work

• Access to telephone and computer or smartphone

• Willing and able to provide adequate information for locator purposes

Exclusion Criteria: Urologic-Specific

• Presence of a neurological condition (e.g., MS, Parkinson's disease, paraplegia) affecting the bladder

• The presence of a symptomatic urethral stricture (males only)

• History of cystitis caused by tuberculosis or radiation or chemotherapies

• Participant has been diagnosed and treated for a pelvic-related malignancy (colon, bladder, prostate, ovarian, endometrial, uterine, testicular, penile, cervical, vaginal, or rectal cancer)

Exclusion Criteria: General

• Participant has a medical condition(s) whose nature or severity (unstable, life threatening, etc.) would influence adversely the conduct of the clinical trial, confound interpretation of study results, and/or compromise volunteer safety and engagement with study demands.

• Gross cognitive impairment, deafness, blindness, vision problems (severe), hearing problems (severe)

• Has a major psychiatric disorder which would impede conduct of the clinical study. These clinical disorders would include but are not limited to major depression with a high risk of suicidal behavior (i.e. intent or plan), current or recent (within the past 3 months) history of alcohol or substance abuse/dependence, a lifetime history of schizophrenia or schizoaffective disorder; or organic mental disorder

• Current involvement in psychotherapy directed specifically toward relief of urological symptoms

• Schedule does not permit participation in clinic sessions or home practice including plans to move out of the area, lack of reliable transportation, etc.

• Characteristics related to inability to complete the study protocol

• Unable to read or fluently speak English

• Inability to complete screening visits

• Inaccessible for interventions and/or follow up evaluations

Related Conditions & MeSH terms

• Bladder Pain Syndrome
• Chronic Pain
• Chronic Pelvic Pain Syndrome
• Chronic Prostatitis
• Cystitis
• Cystitis, Interstitial
• Interstitial Cystitis
• Pelvic Pain
• Prostatitis
• Somatoform Disorders
• Syndrome

Intervention

Behavioral:
• Minimal Contact-Cognitive Behavior Therapy
This 4 session largely home-based version of CBT with minimal therapist contact treatment is aimed at improving UCPPS symptoms by teaching symptom self-management skills that modify illness beliefs, information processing strategies, and reactions that aggravate pelvic pain and urinary symptoms.
• Patient Education/Support
This 4 session largely home-based treatment is aimed at improving UCPPS symptoms through the provision of support and science-based information about UCPPS symptoms, how it is diagnosed, its causes, impacts, and triggers, treatment options and a collaborative relationship between the patient and clinician.

Locations

Country	Name	City	State
United States	University of Michigan	Ann Arbor	Michigan
United States	University at Buffalo (the only clinical site where treatment is delivered)	Buffalo	New York
United States	UCLA	Los Angeles	California

Sponsors (3)

Lead Sponsor	Collaborator
State University of New York at Buffalo	University of California, Los Angeles, University of Michigan

Country where clinical trial is conducted

United States, 

References & Publications (2)

Clemens JQ, Mullins C, Ackerman AL, Bavendam T, van Bokhoven A, Ellingson BM, Harte SE, Kutch JJ, Lai HH, Martucci KT, Moldwin R, Naliboff BD, Pontari MA, Sutcliffe S, Landis JR; MAPP Research Network Study Group. Urologic chronic pelvic pain syndrome: insights from the MAPP Research Network. Nat Rev Urol. 2019 Mar;16(3):187-200. doi: 10.1038/s41585-018-0135-5. — View Citation

Leue C, Kruimel J, Vrijens D, Masclee A, van Os J, van Koeveringe G. Functional urological disorders: a sensitized defence response in the bladder-gut-brain axis. Nat Rev Urol. 2017 Mar;14(3):153-163. doi: 10.1038/nrurol.2016.227. Epub 2016 Dec 6. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	PROMIS - Fatigue SF-7a	7-item measure of range of symptoms, from mild subjective feelings of tiredness to an overwhelming, debilitating, and sustained sense of exhaustion that likely decreases one's ability to execute daily activities and function normally in family or social roles. Fatigue is an IMMPACT-recommended endpoint	Baseline, 12 weeks after pre treatment baseline, 3- and 6-month follow-up
Other	PROMIS Scale v1.2-Global Health Physical 2a	2-item measure of global physical health	Baseline, 12 weeks after pre treatment baseline, 3- and 6-month follow-up
Other	PROMIS Scale v1.2-Global Health Mental 2a	2-item measure of global mental health	Baseline, 12 weeks after pre treatment baseline, 3- and 6-month follow-up
Other	Beck Depression Inventory - II (BDI-II)	21-item criteria-referenced questionnaire of depressive severity. The BDI is aan IMMPACT-recommended measure.	Baseline, 12 weeks after pre treatment baseline, 3- and 6-month follow-up
Other	SF-12 Health Survey	12-item generic QOL measure of eight domains of health (physical functioning, role limitations from physical health, bodily pain, general health perceptions, vitality, social functioning, role limitations resulting from emotional problems, mental health). The SF-12 include an IMMPACT-recommended role functioning item	Baseline, 12 weeks after pre treatment baseline, 3- and 6-month follow-up
Other	Change from baseline of the PROMIS - Sleep Disturbance SF-8b	8-item measure of perceptions of sleep quality, sleep depth, and restoration associated with sleep. Sleep is an IMMPACT-recommended endpoint	Baseline, 12 weeks after pre treatment baseline, 3- and 6-month follow-up
Primary	Clinical Global Impressions - Improvement Scale Patient Version (CGI-I)	Widely used measure of global improvement of symptoms from baseline. To optimize rigor, clinician version by independent MD assessors "blind" to treatment assignment will also measure global severity of pelvic pain and urinary symptoms from baseline and validate patient-reported global improvement as a marker of clinical response. Global improvement is a core domain recommended for conducting clinical trials of the efficacy and effectiveness of treatments for chronic pain according to Initiative on Methods, Measurement, and Pain Assessment in Clinical Trials (IMMPACT)	12 weeks after pre-treatment baseline
Secondary	Genitourinary Pain Index (GUPI)	9-item instrument of genitourinary pain including three subscales: pain, urinary, quality of life, and a total score. The GUPI includes a pain rating scale (assessed by a 0 to 10 numerical rating scale) which is a core outcome domain recommended for conducting clinical trials of the efficacy and effectiveness of treatments for chronic pain according to Initiative on Methods, Measurement, and Pain Assessment in Clinical Trials (IMMPACT)	Baseline, 12 weeks after pre treatment baseline, 3- and 6-month follow-up
Secondary	Interstitial Cystitis Problem Index (ICPI)	4-item questionnaire assessing problems caused by urinary and pelvic pain symptoms	Baseline, 12 weeks after pre treatment baseline, 3- and 6-month follow-up
Secondary	Interstitial Cystitis Symptom Index (ICSI)	4-item questionnaire of urinary and pelvic pain symptoms	Baseline, 12 weeks after pre treatment baseline, 3- and 6-month follow-up
Secondary	Brief Symptom Inventory (BSI 18)	18-item measure of anxiety, depression, somatization and overall distress. Emotional distress is a core IMMPACT domain recommended for conducting clinical trials of the efficacy and effectiveness of treatments for chronic pain	Baseline, 12 weeks after pre treatment baseline, 3- and 6-month follow-up
Secondary	PROMIS - Pain Interference SF-6a	6-item measure of consequences of pain on relevant aspects of one's life, including the extent to which pain hinders engagement with social, cognitive, emotional, physical, and recreational activities. Physical functioning is a core IMMPACT domain recommended for conducting clinical trials of the efficacy and effectiveness of treatments for chronic pain	Baseline, 12 weeks after pre treatment baseline, 3- and 6-month follow-up
Secondary	Client Satisfaction Questionnaire (CSQ)	8-item questionnaire of patient satisfaction with treatment services. Patient satisfaction is a core IMMPACT domain recommended for conducting clinical trials of the efficacy and effectiveness of treatments for chronic pain	12 weeks after pre treatment baseline