Skip to main content
Clinical Trials/NCT03238716
NCT03238716
Terminated
Not Applicable

Neuromuscular Re-education, Impairment-based Exercise and Electric Dry Needling vs. Neuromuscular Re-education and Impairment-based Exercise for Stress Urinary Incontinence

Alabama Physical Therapy & Acupuncture1 site in 1 country24 target enrollmentJuly 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stress Urinary Incontinence
Sponsor
Alabama Physical Therapy & Acupuncture
Enrollment
24
Locations
1
Primary Endpoint
Incontinence Impact Questionnaire - Short Form IIQ-7
Status
Terminated
Last Updated
6 years ago

Overview

Brief Summary

The purpose of this research is to compare two different approaches for treating patients with stress urinary incontinence: neuromuscular re-education, impairment-based exercise and electric dry needling versus neuromuscular re-education and impairment-based exercise. Physical therapists commonly use all of these techniques to treat stress urinary incontinence. This study is attempting to find out if one treatment strategy is more effective than the other.

Detailed Description

Patients with stress urinary incontinence will be randomized to receive 2 treatment sessions per week for up to 6 weeks (8-12 sessions total) of either: (1) neuromuscular re-education, impairment-based exercise and electric dry needling (2) neuromuscular re-education and impairment-based exercise

Registry
clinicaltrials.gov
Start Date
July 1, 2017
End Date
May 1, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Alabama Physical Therapy & Acupuncture
Responsible Party
Principal Investigator
Principal Investigator

James Dunning, DPT, MSc, FAAOMPT

Primary Investigator and President of Spinal Manipulation Institute and Dry Needling Institute of the American Academy of Manipulative Therapy

Alabama Physical Therapy & Acupuncture

Eligibility Criteria

Inclusion Criteria

  • Aged 35 - 75 years
  • Meet the diagnosis of stress urinary incontinence - urine leakage with increased abdominal pressure from laughing, sneezing, coughing, or other physical stressors on abdominal cavity and bladder

Exclusion Criteria

  • Urge urinary incontinence or mixed urinary incontinence
  • Greater than second degree prolapse
  • Previous surgical intervention related to female anatomy
  • Urinary tract infection
  • Unable to participate in movement such as walking, stair climbing, or resistance training
  • Taking medication that impacts bladder function
  • Serious cardiovascular, cerebral disease, psychiatric disorder, cognitively impaired, injury of cauda equine, and/or myelopathy
  • Sacral nerve stimulator implanted
  • Cardiac pacemaker, metal allergy, or severe needle phobia

Outcomes

Primary Outcomes

Incontinence Impact Questionnaire - Short Form IIQ-7

Time Frame: baseline, 6 weeks, 3 months

7 questions, each worth 0-3 points. The average score of items responded to is calculated, then multiplied by 33 1/3 to put the scores on a scale of 0 to 100. High scores indicate greater impact of incontinence.

Secondary Outcomes

  • Urinary pad per day usage(baseline, 6 weeks, 3 months)
  • Urogenital Distress Inventory(baseline, 6 weeks, 3 months)
  • Global Rating of Change Scale(6 weeks, 3 months)

Study Sites (1)

Loading locations...

Similar Trials