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NCT Number: NCT05750212

Musculoskeletal and Pelvic Floor Health in Female Chronic Overlapping Pelvic Pain Conditions

The purpose of this study is to learn about nerve function and pelvic muscle function. To do this we will compare the pelvic nerve and muscle function of women with chronic pelvic pain to those who do not have chronic pelvic pain. Understanding the pain may lead to better treatments in the future.

Recruiting

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Key information

Age range

21 year–80 year

Sex eligibility

Female

Study type

Observational

Primary location

Loyola Medical Center

Maywood, Illinois, 60153, United States

Location status: Recruiting

Location contact

Mary Tulke, RN

CONTACT

[email protected]

7082162067

About this study

Chronic pelvic pain (CPP) may affect up to a quarter of all women. Traditionally, CPP has been thought to be driven by visceral pain mechanisms such as Interstitial Cystitis/Painful Bladder Syndrome (IC/PBS), Irritable bowel syndrome (IBS) and endometriosis. It is also established that these visceral pain conditions overlap with vulvodynia, fibromyalgia, depression, and anxiety. More recently, underlying pelvic floor myofascial (PFMP) and dyssynergia have been identified as additional overlapping CPP conditions. Prior work suggests PFMP may be a viscero-somatic response, however, PFMP as a compensatory consequence of other regional musculoskeletal (MSK) conditions has also been proposed. Indeed, across their lifespan, women face higher risks than men for a plethora of MSK injuries and chronic MSK conditions, including an increased prevalence of sports-related injuries, joint hypermobility, fibromyalgia, osteoarthritic conditions (post-menopause), and osteoporosis/osteoporosis-associated fractures. These elevated risks are thought to be due to the unique anatomic (structural), biomechanical, and hormonal factors that can be attributed to the physiologic process of pregnancy and aging. The current application aims to address the significant knowledge gap regarding the limited understanding of the neuromuscular function of the PFM in CPP as well as the role of overlapping MSK conditions and MSK health that may be influencing PFM response. The short-term goal is to examine PFM biomechanics by identifying the most precise muscle measures in women with CPP of various overlapping diagnoses compared to asymptomatic controls, along with assessing overall MSK health/physical activity. The long-term goal is to determine MSK pelvic pain mechanisms that will inform clinically relevant classification, develop evidence-based non-pharmacologic (physical therapy/exercise) treatments for women with CPP, and advance research tools in the area of PFM function and CPP as it relates to overall MSK health. Our innovative strategy combines neuromuscular measures using novel devices and validated measures in evaluating CPP, MSK health, and physical activity. Our central hypothesis is that women with CPP will demonstrate quantifiable PFM abnormalities and clinical MSK characteristics that differ from asymptomatic controls. The results from this study will have a significant public health impact with contributions of rigorous objective and comprehensive PFM and MSK methods, which will be suitable for future NIH clinical research networks/trials, to evaluate and assess the MSK contribution and potential treatment outcomes in women with CPP.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female sex
  • Age 21 to 80 years
  • Symptoms of CPP as defined by the American College of Obstetrics & Gynecology (ACOG) for more than 6 months
  • At least two of seven overlapping CPP diagnosis (i.e., IC/PBS, IBS, Endometriosis, Vulvodynia, PN, FM, PFMP)
  • An average CPP pain score of at least three on a 10 point pain scale

Exclusion criteria

  • Current or history of GI or GU pelvic cancer
  • Current pelvic infection (e.g., a UTI or vaginal infection)
  • Current or imminent planned pregnancy or recent delivery in the last 6 months
  • Abdominal or pelvic surgery in the last 36 months.

Treatment and study plan

Tone

Diagnostic Test

Tone is a binary measurement of the pelvic floor muscle on physical examination

Tenderness

Diagnostic Test

Tenderness is a binary measurement of the pelvic floor muscle on physical examination

Contraction

Diagnostic Test

Contraction is a binary measurement of the pelvic floor muscle on physical examination

Relaxation

Diagnostic Test

Relaxation is a binary measurement of the pelvic floor muscle on physical examination

Electromyography

Diagnostic Test

Electromyography is a measurement of the pelvic floor muscle in microvolts

Transperineal

Diagnostic Test

Transperineal measurements (in millimeters) of the pelvic floor muscle using an ultrasound

Pressure

Diagnostic Test

Pressure measurements (in millimeters) of the pelvic floor muscle using an algometer

Primary outcomes

  1. Difference in two receiver operating characteristic curves

    Time frame: 0 Days

    The delta value between two diagnostic accuracy statistics (c-statistics) will be reported with its 95% confidence interval and significance value (p-value).

Study contacts

Contact information is provided by the study sponsor or research team.

Colleen Fitzgerald, MD

CONTACT

[email protected]

7082163387

Mary J Tulke, RN

CONTACT

[email protected]

7082162067

Sponsors and collaborators

Lead sponsor

Loyola University

Other

Registry information

Official study title

Musculoskeletal and Pelvic Floor Health in Female Chronic Overlapping Pelvic Pain Conditions (The MSK-PELVIC Study)

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Mar 1, 2023
Registry last updated
Mar 10, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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