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Self-Care to Prevent Birth-Related Urinary Incontinence in Diverse Women

This study is ongoing, but not recruiting participants.
Sponsor:
Collaborator:
Information provided by (Responsible Party):
Carolyn Sampselle, University of Michigan
ClinicalTrials.gov Identifier:
NCT00763984
First received: September 30, 2008
Last updated: June 21, 2013
Last verified: June 2013
  Purpose

The primary goal of this project is to determine the efficacy of an antenatal Bladder Health class to prevent UI in a diverse sample of African American, Caucasian, and Hispanic childbearing women. The determination of efficacy will be made at 12-months post index birth, a time point that is a traditional benchmark of recovery from childbirth, using UI incidence/severity as the primary outcome.


Condition Intervention Phase
Post-Partum Urinary Incontinence
Behavioral: Usual Care
Behavioral: Bladder Health class
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single Blind (Caregiver)
Primary Purpose: Prevention
Official Title: PERL 4: Promoting Effective Recovery From Labor

Resource links provided by NLM:


Further study details as provided by University of Michigan:

Primary Outcome Measures:
  • UI incidence/severity [ Time Frame: 12 months - 3 years post-index birth ] [ Designated as safety issue: No ]

Estimated Enrollment: 612
Study Start Date: October 2007
Estimated Study Completion Date: December 2013
Estimated Primary Completion Date: December 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: 1 Behavioral: Usual Care
This group will receive routine care, however, it is possible that that control condition participants will receive Pelvic Floor Muscle Training (PFMT) instruction from their health care providers. We will monitor control women's knowledge, adoption and maintaining of PFMT.
Experimental: 2 Behavioral: Bladder Health class
Modeled on our intervention with older women, Bladder Health Class (BH Class) will include Pelvic floor muscle training (PFMT), defined by the International Continence Society as repetitive selective voluntary contraction and relaxation of specific pelvic floor muscles, and bladder training (BT), defined as a program of scheduled voiding with gradually progressive voiding intervals. The BT instructions will be modified for this pregnant group. We will monitor control women's knowledge, adoption and maintaining of PFMT and BT.

Detailed Description:

This study is significant because UI prevalence is 34% overall among US women, nearly half of whom consider their incontinence to be moderately to extremely bothersome. UI is 2.0 to 2.6 fold greater in women after pregnancy and childbirth as compared to their never pregnant counterparts, with the incidence increasing after each child. UI impact increases as women age extending into middle and later life. The financial cost of UI in the United States exceeds $19 billion per year . Other costs are identified in the Healthy People 2010 report 22 and include: 1) decreased activity/ fitness, which can be seriously affected because women who are concerned about accidental leakage markedly curtail physical activity and 2) increased depression, which has been linked to UI in women. Women are at least twice as likely as men to have UI; pregnancy and childbirth are major explanatory factors. In perimenopausal women, prevalence of any UI was 57% and of moderate to severe UI was 25%; after controlling for age, race/ethnicity, menopausal status and body mass index, parity persisted as a significant predictor of UI with an OR of 1.62 (CI 1.31, 2.01).

Noninvasive interventions during the period of childbearing are of particular interest for UI prevention in women. Two self-management practices recommended for the initial treatment of UI are: Pelvic floor muscle training (PFMT), defined by the International Continence Society as repetitive selective voluntary contraction and relaxation of specific pelvic floor muscles, and bladder training (BT), defined as a program of scheduled voiding with gradually progressive voiding intervals. The Knack Maneuver (a preemptive pelvic floor muscle contraction to decrease stress UI and/or suppress urge UI) has demonstrated efficacy in older women diagnosed with UI. In childbearing women, only PFMT has been tested with a rigorous RCT design. We taught PFMT, the Knack, and BT as a combined strategy to older women and found a two-fold prevention effect. The proposed project is innovative because it will be the first to our knowledge to test the preventive capacity of an intervention in childbearing women that combines PFMT, the Knack, and BT. This project is also innovative because it will be conducted with a diverse sample of primiparous/multiparous women, using a 3-year follow-up period. Because PFMT is the only self-management strategy that is currently recommended practice for maternity patients, we will use PFMT adherence in comparisons between the treatment and control conditions

Recruitment and Informed Consent:

Fliers specifying eligibility criteria and benefits of research participation will be prominently displayed in the waiting areas and in the women's bathrooms of the respective clinical sites. Potential participants will be invited to speak with a designated site-based contact re: what participation in the study would entail. This individual will answer initial questions, review written material that describes study participation, conduct verbal screening, and obtain informed consent from eligible individuals. Eligible participants will be scheduled for a clinic visit at the respective site for a clinic visit to obtain clinical verification of no objective incontinence (negative standing stress test) and evidence of ability to contract the pelvic floor correctly (digital measure). Following determination of eligibility, participants will be randomized into control (routine care) or treatment (scheduled for Bladder Health class) condition.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

Women who are pregnant and expecting their first, second, or third baby are eligible if they:

  • are age eighteen years or older
  • are able to understand and read English or Spanish
  • are low risk antepartum (first, second or third pregnancy)
  • are 16-25 weeks pregnant
  • expect a vaginal birth
  • have lost no more than a few drops of urine as often as every other day
  • have no previous or current urinary incontinence treatment with medication, formal behavioral programs or surgery
  • have no history of bladder cancer, diabetes, stroke, multiple sclerosis, muscular dystrophy, cerebral palsy, Parkinson's, epilepsy, or trauma of the spinal cord
  • Do not have (or have not had within the last 3 years) *chronic urinary tract infection. *Chronic is defined as having more than 3 urinary tract infections in one year.

Exclusion Criteria:

  • If participant does not meet all of the above criterion for inclusion
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00763984

Locations
United States, Michigan
University of Michigan Health System
Ann Arbor, Michigan, United States, 48109
Jackson Center for Family Health
Jackson, Michigan, United States, 49202
La Clinica de la Santa Teresa
Pontiac, Michigan, United States, 48341
Sponsors and Collaborators
University of Michigan
Investigators
Principal Investigator: Carolyn Sampselle, PhD, RNC, FAAN University of Michigan, School of Nursing, Grants and Research Office
  More Information

No publications provided

Responsible Party: Carolyn Sampselle, Carolyne K. Davis Professor of Nursing, University of Michigan
ClinicalTrials.gov Identifier: NCT00763984     History of Changes
Other Study ID Numbers: 2R01NR007618-06A1, R01NR007618, 2R01NR007618-06A1, HUM00015712
Study First Received: September 30, 2008
Last Updated: June 21, 2013
Health Authority: United States: Federal Government

Keywords provided by University of Michigan:
Bladder Control for Women
Exercising Your Pelvic Muscles
Kegel Exercises: How to Strengthen Pelvic Floor Muscles
Kegel Exercises for Your Pelvic Muscles
Pelvic Floor Disorders
Pelvic Support Problems
Pregnancy
Pregnancy Childbirth and Bladder Control
Urinary Incontinence
Urinary Incontinence: Embarrassing but Treatable

Additional relevant MeSH terms:
Urinary Incontinence
Lower Urinary Tract Symptoms
Signs and Symptoms
Urination Disorders
Urologic Diseases
Urological Manifestations

ClinicalTrials.gov processed this record on November 20, 2014