Actively Recruiting

Phase Not Applicable
Age: 18Years - 35Years
FEMALE
Healthy Volunteers
NCT07209566

A Research Study Exploring How Musculoskeletal Function and the Autonomic Nervous System Relate to Visceral Pain in Women With and Without Dysmenorrhea (Painful Periods).

Led by Azusa Pacific University · Updated on 2025-10-07

60

Participants Needed

1

Research Sites

86 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this clinical trial is to determine if women with dysmenorrhea demonstrate an increased musculoskeletal and autonomic nervous system response to a painful visceral stimulus compared to controls. A secondary aim is to determine if interoceptive awareness moderates this relationship. The designed methodology aims to elucidate the intricate connections between the interoceptive and musculoskeletal systems in pain perception among female participants, providing valuable insights into the underlying mechanisms of interoceptive pain and functional musculoskeletal changes.

CONDITIONS

Official Title

A Research Study Exploring How Musculoskeletal Function and the Autonomic Nervous System Relate to Visceral Pain in Women With and Without Dysmenorrhea (Painful Periods).

Who Can Participate

Age: 18Years - 35Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Non-pregnant women
  • Not taking hormonal birth control
  • Between the ages of 18 and 36
  • Report regular menstrual cycles
Not Eligible

You will not qualify if you...

  • Currently pregnant
  • Gave birth within the last six months
  • Breastfeeding
  • Undergoing in-vitro fertilization treatments
  • Had abdominal, lumbar, or pelvic surgery within the last 12 months
  • Have chronic pain conditions
  • Have an active genitourinary infection
  • Incontinent of bowel or bladder
  • Diagnosed with pelvic organ prolapse, severe labral pathology, femoral acetabular impingement, interstitial cystitis, endometriosis, pelvic inflammatory disease, irritable bowel syndrome, or other pelvic pathology
  • Cycle length less than 28 days or longer than 35 days
  • History of sexual assault
  • Anovulatory without hormonal birth control or amenorrheic

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Azusa Pacific University

Azusa, California, United States, 91702

Actively Recruiting

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Research Team

M

Megan M Steele, PT, DPT, PhD(c)

CONTACT

J

Jennifer Fernandez, PT, DPT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

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