search
Back to results

Acupuncture for Urinary Incontinence

Primary Purpose

Urinary Incontinence

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Acupuncture
Sham acupuncture
Sponsored by
University of Pittsburgh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urinary Incontinence focused on measuring urinary incontinence

Eligibility Criteria

25 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Urge or stress urinary incontinence at least twice a week on average for at least 3 months Exclusion Criteria: History of previous acupuncture History of a neurologic problem such as Parkinson's disease or multiple sclerosis that could affect bladder function Current treatment with overactive bladder medications or medications that relax the bladder Urinary catheter Pregnancy Inability to empty the bladder effectively Inability to toilet independently Current treatment with steroid Interstitial cystitis Chronic pelvic pain Current treatment with warfarin

Sites / Locations

  • University of Pittsburgh

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Acupuncture

Sham acupuncture

Arm Description

Subjects will 12 acupuncture treatments over 6 weeks; treatment sessions occur twice a week. A total of 12 acupuncture needles will be inserted bilaterally at two leg points and four back points. Needles are manually inserted through a standard guide tube contained within a fitted sheath and the basal ring secured to the skin by double-sided tape. The needles remain in place for 25 minutes and are manually stimulated twice during each treatment.

Subjects will receive 12 sham acupuncture treatments (delivered twice a week) over 6 weeks. The sham needle is blunted needle whose shaft telescopes into the handle when tapped. While the needle appears to have been inserted, it does not actually penetrate the skin. It is held in place by the same standard guide tube used in the true acupuncture group. The acupuncture points and duration of treatment are the same as for the true acupuncture group.

Outcomes

Primary Outcome Measures

Percent Change in Incontinent Episodes
Percent change in incontinent episodes (measured by self-report electronic bladder diary) at 1 week post-intervention (true or sham acupuncture) relative to baseline.
Percent Change in Incontinent Episodes
Percent change in incontinent episodes (measured by self-report electronic bladder diary) 4 weeks post true or sham acupuncture
Physical Health-Related Quality of Live
Percent change in physical health related quality of life measured at 1 week post-intervention (true or sham acupuncture) relative to baseline; measured by the Medical Outcomes Study Short Form-36 (SF-36) Physical Component score. Higher SF-36 Physical Component scores are considered a better outcome.
Physical Health-Related Quality of Life
Percent change in physical health related quality of life measured at 4 weeks post intervention (true or sham acupuncture) relative to baseline; measured by the Medical Outcomes Study Short Form-36 (SF-36) Physical Component score. Positive change indicates an increase in physical health-related quality of life.
Mental Health Related Quality of Life
Percent change in mental health related quality of life measured at 1 week1 post intervention (true or sham acupuncture) relative to baseline; measured by the Medical Outcomes Study Short Form-36 (SF-36) Mental Health Component score. Higher Mental Health Component scores are considered a better outcome.
Mental Health Related Quality of Life
Percent change in mental health related quality of life measured at 4 weeks post intervention (true or sham acupuncture) relative to baseline; measured by the Medical Outcomes Study Short Form-36 (SF-36) Mental Health Component score.
Incontinence-Specific Quality of Life
Percent change in incontinence specific quality of life at 1 week post intervention (true or sham acupuncture) as measured by the Incontinence Impact Questionnaire. Positive values indicate improvement in incontinence-specific quality of life.
Incontinence-Specific Quality of Life
Percent change in incontinence-specific quality of life a 4 weeks post-intervention (true or sham acupuncture) measured by the Incontinence Impact Questionnaire. Positive changes indicate improvement in incontinence-specific quality of life.
Duration of Any Beneficial Effects
Time to relapse in months of participants who completed true acupuncture initially or who crossed-over following sham (offered to all sham participants)

Secondary Outcome Measures

Change in Bladder Capacity
Measured by filling the bladder with sterile fluid until until the subject reported a strong urge to urinate.
Urodynamic Diagnostic Impression of Stress Urinary Incontinence
Documentation of a diagnostic impression of stress urinary incontinence following urodynamics
Urodynamic Impression of Urge Urinary Incontinence
Documentation of a diagnostic impression of urge urinary incontinence following urodynamics
Characteristics of Responders Based on Glasses/Cups Per Day of Non-caffeinated Fluids (Including Water)
Glasses/cups per day of non-caffeinated fluids (including water) at baseline
Characteristics of Responders: Duration of Urinary Incontinence (UI) in Years
Duration of urinary incontinence in years
Adherence to Treatment Protocol
Percentage of acupuncture (true or sham) visits completed as scheduled
Burden Associated With the Acupuncture Treatment Protocol
Subjects' report of burden (difficulty) associated with the frequency, number and duration of treatment) and the position they had to remain in during the true and sham treatments. Subjects rate the difficulty associated with each of the four aspects of treatment on a 10-point scale ranging from 1 (not at all difficult) to 10 (extremely difficult). The burden score was calculated as the average of the scores on the 4 items with a possible range of 1 to 10 with higher scores indicating greater burden.
Need for Booster Acupuncture During Follow-up
The number of participants who were received true acupuncture (as their initial intervention or after initially receiving sham acupuncture) and were eligible to receive a booster (had a 50% or greater reduction in incontinent episodes following true acupuncture) and completed at least one month of follow-up and experienced a 30% or greater increase in incontinent episodes during follow up.
Response to Booster Acupuncture if Needed
Change in the number of incontinent episodes per day following booster acupuncture
Pelvic Floor Muscle Strength
Change in average duration of pelvic floor muscle contraction measured by electromyography. Subjects were instructed to tighten their pelvic floor muscles when prompted and hold the contraction until told to relax (up to 10 seconds). This was repeated three times and the duration of the contraction time was averaged.
Pelvic Floor Muscle Strength
Change in average duration of pelvic floor muscle contraction measured by electromyography. Subjects were instructed to tighten their pelvic floor muscles when prompted and hold the contraction until told to relax (up to 10 seconds). This was repeated three times and the duration of the contraction time was averaged.

Full Information

First Posted
February 24, 2006
Last Updated
August 31, 2016
Sponsor
University of Pittsburgh
Collaborators
National Center for Complementary and Integrative Health (NCCIH)
search

1. Study Identification

Unique Protocol Identification Number
NCT00297427
Brief Title
Acupuncture for Urinary Incontinence
Official Title
Efficacy of Acupuncture in Treating Urinary Incontinence
Study Type
Interventional

2. Study Status

Record Verification Date
August 2016
Overall Recruitment Status
Completed
Study Start Date
October 2005 (undefined)
Primary Completion Date
May 2011 (Actual)
Study Completion Date
July 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pittsburgh
Collaborators
National Center for Complementary and Integrative Health (NCCIH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This research study will evaluate the effectiveness of acupuncture in decreasing urinary incontinence (involuntary urine loss) in women. The study will involve 12 acupuncture sessions over 6 weeks. We will compare the effectiveness of acupuncture and sham (placebo) acupuncture (a procedure in which the needle feels like it penetrates the skin, but is not actually inserted into the body) on the frequency and volume of involuntary (accidental) urine loss after completing the intervention, and again one month later. Individuals participating in this study will be randomly assigned to receive either the actual or sham acupuncture. Randomization means being assigned by chance, similar to flipping a coin. Study participants will not know which group (actual or sham acupuncture) they were assigned to until one month after completing the 6-weeks of treatment. The sham acupuncture needles look similar to the real acupuncture needles and feel like they penetrate the skin, but do not actually do so. If individuals are assigned to the sham acupuncture group, they will be eligible to receive the actual acupuncture one month after completing the sham acupuncture if they wanted to. All individuals will be followed for 6 months after completing the acupuncture treatments.
Detailed Description
See Brief Summary

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Incontinence
Keywords
urinary incontinence

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
127 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Acupuncture
Arm Type
Experimental
Arm Description
Subjects will 12 acupuncture treatments over 6 weeks; treatment sessions occur twice a week. A total of 12 acupuncture needles will be inserted bilaterally at two leg points and four back points. Needles are manually inserted through a standard guide tube contained within a fitted sheath and the basal ring secured to the skin by double-sided tape. The needles remain in place for 25 minutes and are manually stimulated twice during each treatment.
Arm Title
Sham acupuncture
Arm Type
Sham Comparator
Arm Description
Subjects will receive 12 sham acupuncture treatments (delivered twice a week) over 6 weeks. The sham needle is blunted needle whose shaft telescopes into the handle when tapped. While the needle appears to have been inserted, it does not actually penetrate the skin. It is held in place by the same standard guide tube used in the true acupuncture group. The acupuncture points and duration of treatment are the same as for the true acupuncture group.
Intervention Type
Procedure
Intervention Name(s)
Acupuncture
Intervention Description
Acupuncture twice weekly for 6 weeks.
Intervention Type
Other
Intervention Name(s)
Sham acupuncture
Intervention Description
Twice a week for 6 weeks
Primary Outcome Measure Information:
Title
Percent Change in Incontinent Episodes
Description
Percent change in incontinent episodes (measured by self-report electronic bladder diary) at 1 week post-intervention (true or sham acupuncture) relative to baseline.
Time Frame
Baseline to 1 Week post-intervention
Title
Percent Change in Incontinent Episodes
Description
Percent change in incontinent episodes (measured by self-report electronic bladder diary) 4 weeks post true or sham acupuncture
Time Frame
4 weeks post true or sham acupuncture
Title
Physical Health-Related Quality of Live
Description
Percent change in physical health related quality of life measured at 1 week post-intervention (true or sham acupuncture) relative to baseline; measured by the Medical Outcomes Study Short Form-36 (SF-36) Physical Component score. Higher SF-36 Physical Component scores are considered a better outcome.
Time Frame
1 Week post-intervention
Title
Physical Health-Related Quality of Life
Description
Percent change in physical health related quality of life measured at 4 weeks post intervention (true or sham acupuncture) relative to baseline; measured by the Medical Outcomes Study Short Form-36 (SF-36) Physical Component score. Positive change indicates an increase in physical health-related quality of life.
Time Frame
4-weeks post-intervention
Title
Mental Health Related Quality of Life
Description
Percent change in mental health related quality of life measured at 1 week1 post intervention (true or sham acupuncture) relative to baseline; measured by the Medical Outcomes Study Short Form-36 (SF-36) Mental Health Component score. Higher Mental Health Component scores are considered a better outcome.
Time Frame
1 week post-intervention
Title
Mental Health Related Quality of Life
Description
Percent change in mental health related quality of life measured at 4 weeks post intervention (true or sham acupuncture) relative to baseline; measured by the Medical Outcomes Study Short Form-36 (SF-36) Mental Health Component score.
Time Frame
4 weeks post true or sham acupuncture
Title
Incontinence-Specific Quality of Life
Description
Percent change in incontinence specific quality of life at 1 week post intervention (true or sham acupuncture) as measured by the Incontinence Impact Questionnaire. Positive values indicate improvement in incontinence-specific quality of life.
Time Frame
1 Week post-intervention
Title
Incontinence-Specific Quality of Life
Description
Percent change in incontinence-specific quality of life a 4 weeks post-intervention (true or sham acupuncture) measured by the Incontinence Impact Questionnaire. Positive changes indicate improvement in incontinence-specific quality of life.
Time Frame
4-weeks post-intervention
Title
Duration of Any Beneficial Effects
Description
Time to relapse in months of participants who completed true acupuncture initially or who crossed-over following sham (offered to all sham participants)
Time Frame
monthly during follow-up up to 6 months
Secondary Outcome Measure Information:
Title
Change in Bladder Capacity
Description
Measured by filling the bladder with sterile fluid until until the subject reported a strong urge to urinate.
Time Frame
Change from baseline to 4 weeks post-intervention
Title
Urodynamic Diagnostic Impression of Stress Urinary Incontinence
Description
Documentation of a diagnostic impression of stress urinary incontinence following urodynamics
Time Frame
Baseline and 4 weeks post-treatment
Title
Urodynamic Impression of Urge Urinary Incontinence
Description
Documentation of a diagnostic impression of urge urinary incontinence following urodynamics
Time Frame
Baseline and 4 weeks post true or sham acupuncture
Title
Characteristics of Responders Based on Glasses/Cups Per Day of Non-caffeinated Fluids (Including Water)
Description
Glasses/cups per day of non-caffeinated fluids (including water) at baseline
Time Frame
Baseline
Title
Characteristics of Responders: Duration of Urinary Incontinence (UI) in Years
Description
Duration of urinary incontinence in years
Time Frame
Baseline
Title
Adherence to Treatment Protocol
Description
Percentage of acupuncture (true or sham) visits completed as scheduled
Time Frame
6 weeks
Title
Burden Associated With the Acupuncture Treatment Protocol
Description
Subjects' report of burden (difficulty) associated with the frequency, number and duration of treatment) and the position they had to remain in during the true and sham treatments. Subjects rate the difficulty associated with each of the four aspects of treatment on a 10-point scale ranging from 1 (not at all difficult) to 10 (extremely difficult). The burden score was calculated as the average of the scores on the 4 items with a possible range of 1 to 10 with higher scores indicating greater burden.
Time Frame
1 week post-treatment
Title
Need for Booster Acupuncture During Follow-up
Description
The number of participants who were received true acupuncture (as their initial intervention or after initially receiving sham acupuncture) and were eligible to receive a booster (had a 50% or greater reduction in incontinent episodes following true acupuncture) and completed at least one month of follow-up and experienced a 30% or greater increase in incontinent episodes during follow up.
Time Frame
Monthly during the 6 month follow-up period
Title
Response to Booster Acupuncture if Needed
Description
Change in the number of incontinent episodes per day following booster acupuncture
Time Frame
After the booster sessions
Title
Pelvic Floor Muscle Strength
Description
Change in average duration of pelvic floor muscle contraction measured by electromyography. Subjects were instructed to tighten their pelvic floor muscles when prompted and hold the contraction until told to relax (up to 10 seconds). This was repeated three times and the duration of the contraction time was averaged.
Time Frame
Baseline and 1 week post true or sham acupuncture
Title
Pelvic Floor Muscle Strength
Description
Change in average duration of pelvic floor muscle contraction measured by electromyography. Subjects were instructed to tighten their pelvic floor muscles when prompted and hold the contraction until told to relax (up to 10 seconds). This was repeated three times and the duration of the contraction time was averaged.
Time Frame
Baseline and 4 weeks post true or sham acupuncture

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Urge or stress urinary incontinence at least twice a week on average for at least 3 months Exclusion Criteria: History of previous acupuncture History of a neurologic problem such as Parkinson's disease or multiple sclerosis that could affect bladder function Current treatment with overactive bladder medications or medications that relax the bladder Urinary catheter Pregnancy Inability to empty the bladder effectively Inability to toilet independently Current treatment with steroid Interstitial cystitis Chronic pelvic pain Current treatment with warfarin
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sandra Engberg, PhD
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Pittsburgh
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Acupuncture for Urinary Incontinence

We'll reach out to this number within 24 hrs