Urinary Incontinence
Conditions
Keywords
Behavior Therapy, Behavioral Medicine, Behavioral Research, Behavioral Sciences, Combined Modality Therapy, Drug Therapy, Overactive bladder, Treatment Outcome, Urge incontinence, Urinary incontinence
Brief summary
The primary objective of this project is to evaluate whether enhancing drug therapy with components of behavioral training, including pelvic floor muscle rehabilitation, results in better outcomes than drug therapy alone for urge incontinence in community-dwelling women.
Detailed description
Urinary incontinence in women is a major problem with significant medical, psychological, and social consequences. Previous research on urge incontinence, a common form of incontinence, has demonstrated that behavioral and drug interventions are effective, but do not cure most patients. Thus there is a need to improve conservative treatment for urge incontinence in women. The primary objective of this project is to evaluate whether enhancing drug therapy with components of behavioral training, including pelvic floor muscle rehabilitation, results in better outcomes than drug therapy alone for urge incontinence in community-dwelling women. This project is a randomized controlled clinical trial. Sixty-four women with predominantly urge incontinence have been randomized. Stratification and blocked randomization procedures are used to assign a subject to 8 weeks of drug therapy alone or 8 weeks of drug therapy enhanced with components of behavioral training that can be administered in most any outpatient clinic. The drug therapy is extended release oxybutynin, a well-established pharmacologic agent with a state of the art drug delivery system that has the lowest rates of side-effect. The behavioral treatment is an innovative, comprehensive, behavioral training program, which includes pelvic floor muscle rehabilitation, teaching urge suppression and other skills to improve bladder control, and self-monitoring with bladder diaries. Bladder diaries completed by subjects before and after the treatment are used to calculate reduction in the frequency of incontinence. Secondary outcomes measures include a patient satisfaction questionnaire and three impact/quality of life measures (Incontinence Impact Questionnaire, Uro-Genital Distress Index, SF-12 Health Survey). The second objective of the study is to examine the cost-effectiveness of adding behavioral components to drug therapy. With the changing health care environment, there is increased concern with the costs of providing treatment. This project will compare the relative costs and value of combined intervention using the methods of cost-effectiveness analysis, the most widely adopted method for the economic evaluation of health interventions. The third objective of the study is to examine further the mechanisms by which these therapies reduce incontinence, including changes in bladder capacity, thresholds for bladder sensation, pelvic muscle strength, use of pelvic muscles in response to the sensation of urgency and frequency of urination. Pre-post changes in these parameters are measured to examine the effects of the treatment on these variables, and structural equation modeling will be used to examine whether changes in each of these measures are related to treatment outcome.
Interventions
Individually-titrated, extended-release oxybutynin chloride with management of side-effects.
Behavioral training consists of teaching urge suppression strategies and pelvic floor muscle training.
Sponsors
Study design
Eligibility
Inclusion criteria
Participants in this study were ambulatory, community-dwelling women (veterans and nonveterans) with persistent urge or predominantly urge incontinence. Participants must: 1. Be ambulatory. 2. Be able to come to the clinic for treatment. 3. Report urge incontinence. 4. Report incontinence occurring at least twice per week on average. 5. Report incontinence persisting for at least three months. 6. Not have received behavioral therapy in the University of Alabama at Birmingham (UAB) Continence Clinic or Department of Veterans Affairs (VA) Continence Clinic. 7. In the clinical interview, the subject must report involuntary loss of urine associated with a strong desire to void and that the condition has persisted for at least three months. 8. At least two urge accidents on the 7-day baseline bladder diary, and the number of urge accidents must exceed the number of other types of accidents. 9. On urodynamic evaluation, there must be cystometric evidence of bladder dysfunction, either: detrusor instability or maximal cystometric capacity is less than 400 ml.
Exclusion criteria
1. Continual leakage. 2. Urinary tract infection (defined as growth of greater than 10,000 colonies per ml of a urinary pathogen on urine culture). 3. Fecal impaction. 4. Uncontrolled metabolic problem. 5. Post-void residual volume \> 150 ml. 6. Hematuria on microscopic examination in the absence of infection. A urologic consultation will be recommended and enrollment will depend on agreement between the urologist and geriatrician (co-PI) that entry into treatment protocol is not contraindicated. 7. Severe uterine prolapse (prolapse reaching the vaginal introitus). 8. Decompensated congestive heart failure, diagnosed by history or physical exam. 9. Impaired mental status. (\<24 on Folstein's Mini-Mental State Exam). 10. Uncontrolled narrow angle glaucoma. 11. Gastric retention (by medical history). 12. Hypersensitivity to oxybutynin. 13. Current use of anticholinergic agents for detrusor instability. Subjects on these medications will be asked to discontinue them for the duration of the study. Evaluation will be delayed until the drug(s) have been discontinued for 2 weeks. 14. If on diuretic, dose stable for less than three months.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in Incontinent Episodes Immediately Post-treatment | Baseline and immediately post-treatment - week 8 | Percent change from baseline in weekly frequency of incontinent episodes immediately post-treatment, derived from baseline and week 8 seven-day bladder diaries. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Incontinent Episodes at 12-month Follow-up | Baseline and 12 months post-treatment | Percent change from baseline in weekly frequency of incontinent episodes at 12-months post-treatment, derived from baseline and 12-month seven-day bladder diaries |
Countries
United States
Participant flow
Recruitment details
Participants were community-dwelling women with urge predominant incontinence recruited between July 2003 and January 2008.
Pre-assignment details
Of the 166 women enrolled, 58 were found to be ineligible on clinical evaluation, 44 withdrew, and 64 were randomized.
Participants by arm
| Arm | Count |
|---|---|
| Arm 1 drug therapy alone
Extended release Oxybutynin Chloride : Individually-titrated, extended release oxybutynin chloride with management of side-effects. | 32 |
| Arm 2 drug therapy + behavioral training
Extended release Oxybutynin Chloride : Individually-titrated, extended release oxybutynin chloride with management of side-effects.
Behavior Training : Behavioral training consists of teaching urge suppression strategies and pelvic floor muscle training. | 32 |
| Total | 64 |
Baseline characteristics
| Characteristic | Arm 1 | Arm 2 | Total |
|---|---|---|---|
| Age Continuous | 59.3 years STANDARD_DEVIATION 11.2 | 57.4 years STANDARD_DEVIATION 12.6 | 58.4 years STANDARD_DEVIATION 11.9 |
| Ethnicity (NIH/OMB) Hispanic or Latino | 0 Participants | 0 Participants | 0 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 32 Participants | 32 Participants | 64 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Incontinence severity Mild (less than 5 episodes/wk) | 4 participant | 4 participant | 8 participant |
| Incontinence severity Moderate (5-10 episodes/wk) | 7 participant | 10 participant | 17 participant |
| Incontinence severity Severe (> 10 episodes/wk) | 21 participant | 18 participant | 39 participant |
| Incontinence type missing | 0 participants | 1 participants | 1 participants |
| Incontinence type Mixed urge + stress | 7 participants | 5 participants | 12 participants |
| Incontinence type Urge only | 25 participants | 26 participants | 51 participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 6 Participants | 14 Participants | 20 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 26 Participants | 18 Participants | 44 Participants |
| Region of Enrollment United States | 32 participants | 32 participants | 64 participants |
| Sex: Female, Male Female | 32 Participants | 32 Participants | 64 Participants |
| Sex: Female, Male Male | 0 Participants | 0 Participants | 0 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — |
| other Total, other adverse events | 0 / 32 | 0 / 32 |
| serious Total, serious adverse events | 0 / 32 | 0 / 32 |
Outcome results
Change in Incontinent Episodes Immediately Post-treatment
Percent change from baseline in weekly frequency of incontinent episodes immediately post-treatment, derived from baseline and week 8 seven-day bladder diaries.
Time frame: Baseline and immediately post-treatment - week 8
Population: Intention to treat
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Drug Therapy Alone | Change in Incontinent Episodes Immediately Post-treatment | -88.5 percentage change | Standard Deviation 24 |
| Drug Therapy + Behavioral Training | Change in Incontinent Episodes Immediately Post-treatment | -78.3 percentage change | Standard Deviation 32.6 |
Change in Incontinent Episodes at 12-month Follow-up
Percent change from baseline in weekly frequency of incontinent episodes at 12-months post-treatment, derived from baseline and 12-month seven-day bladder diaries
Time frame: Baseline and 12 months post-treatment
Population: Intention to treat
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Drug Therapy Alone | Change in Incontinent Episodes at 12-month Follow-up | -82.0 percent change | Standard Deviation 26.1 |
| Drug Therapy + Behavioral Training | Change in Incontinent Episodes at 12-month Follow-up | -75.2 percent change | Standard Deviation 33.4 |