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Orthopedic Intervention for Chronic Prostatitis/Chronic Pelvic Pain Syndrome

N/A
Waitlist Available
Research Sponsored by Texas Woman's University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up difference between enrollment and end of intervention phase (5 weeks). difference between end of intervention and end of follow-up (2 weeks), immediately before and after dry needling (2 visits per week, weeks 2, 3, 4, 5 of the study)
Awards & highlights
No Placebo-Only Group

Summary

The primary purpose of this study is to establish if an individualized, impairment-based orthopedic intervention (IOI) can improve pelvic floor function and pain in women with Chronic Pelvic Pain (CPP). Dry needling will be used as a part of the IOI to intervene upon peripheral muscles stiffness previously found to be more stiff in this population compared to healthy controls. This study is intended to initiate a line of research aimed at assessing widely used orthopedic physical therapy practices to address orthopedic impairments and muscle stiffness differences in women with CPP potentially decreasing time to care for a widely experienced condition. This study will guide potential future studies aimed at intervening upon a larger population and establishing the characteristics of participants who respond favorable to orthopedic care alone. First, this study will establish if this type of intervention has an effect on pelvic floor function and symptoms, pain, and muscle stiffness, all of which are often priorities of treatment for PHPTs treating CPP. A single-subject design is well suited in studying an intervention on such a heterogeneous patient population that does not currently have physical therapy treatment subclassifications. Future studies could help to establish possible subclassifications of CPP to include an orthopedic or peripheral muscle stiffness classification and empower therapists with associations between peripheral orthopedic and myofascial dysfunction and pelvic floor function and pain. This line of research could help prioritize which patients require specialty care, who could initiate care with an orthopedic PT, and who may resolve dysfunction and pain with orthopedic PT alone.

Eligible Conditions
  • Chronic Prostatitis/Chronic Pelvic Pain Syndrome
  • Chronic Pain
  • Pelvic Pain
  • Muscle Tightness

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~difference between enrollment and end of intervention phase (5 weeks). difference between end of intervention and end of follow-up (2 weeks), immediately before and after dry needling (2 visits per week, weeks 2, 3, 4, 5 of the study)
This trial's timeline: 3 weeks for screening, Varies for treatment, and difference between enrollment and end of intervention phase (5 weeks). difference between end of intervention and end of follow-up (2 weeks), immediately before and after dry needling (2 visits per week, weeks 2, 3, 4, 5 of the study) for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in Muscle stiffness pre- and post- dry needling and before and after the whole intervention
Change in Numeric Pain Rating scale Pre- and Post- the whole orthopedic intervention
Change in Pain Pressure Threshold, pre- and post- dry needling and before and after the whole intervention
Secondary study objectives
Change in Subjective Pelvic floor muscle function Pre- and Post- the whole orthopedic intervention
Other study objectives
Change in Pelvic Floor muscle function via intervaginal examination

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Orthopedic InterventionExperimental Treatment2 Interventions
All subjects are receiving an orthopedic intervention that is specific to their presentation but made up of all intervention categories: Manual therapy, dry needling, deep breathing, stretching, strengthening, and progressive overload.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Dry Needling
2020
Completed Phase 2
~1090

Find a Location

Who is running the clinical trial?

Texas Woman's UniversityLead Sponsor
87 Previous Clinical Trials
5,889 Total Patients Enrolled
~3 spots leftby Nov 2025