Cervical Cancer, Endometrial Cancer, Ovarian Epithelial Cancer, Ovarian Germ Cell Tumor, Uterine Sarcoma, Vulvar Cancer
Conditions
Keywords
Pelvic floor muscle training; incontinence; quality of life
Brief summary
This randomized pilot clinical trial studies pelvic floor muscle training in treating urinary incontinence in gynecologic cancer survivors. Pelvic floor muscle training may help control symptoms and improve physical function and quality of life in gynecologic cancer survivors.
Detailed description
PRIMARY OBJECTIVES: I. To assess whether pelvic floor muscle training and behavioral therapy in gynecologic cancer survivors results in improvement in incontinence symptoms as measured by a validated questionnaire (Patient Global Impression of Improvement) at three month follow-up when compared to women who do not undergo pelvic floor muscle training. II. To evaluate whether women who undergo pelvic floor muscle training and behavioral therapy report greater improvement in validated urinary incontinence symptom severity, pelvic floor distress and quality of life measures than women who do not undergo pelvic floor muscle training. III. To evaluate the acceptability of pelvic floor muscle training (PFMT) among gynecological cancer survivors and to provide preliminary data to inform a power analysis for a larger randomized trial. OUTLINE: Patients are randomized to 1 of 2 treatment arms. ARM I: Patients receive a handout describing behavioral management tips for urinary incontinence, including information and suggestions about optimal volume fluid intake, constipation management, measures to reduce urgency by spreading fluid intake, and avoiding caffeine and other bladder irritants that have proved effective in other intervention trials. Patients undergo PFMT over 20-30 minutes teaching them to contract the pelvic floor muscles correctly and receive feedback to avoid the contraction of abdominal, gluteal or adductor muscles. Patients are asked to perform 3 sets of 10 pelvic muscle contractions with a goal of holding the contraction for 5 seconds daily for 12 weeks and also receive a reminder phone call to address concerns and review the instructions at 4 weeks. ARM II: Patients receive usual care for urinary incontinence, with an option to join the training program after completion of study. After completion of study treatment, patients are followed up at 3 months.
Interventions
OTHERquestionnaire administration
Ancillary studies
PROCEDUREstandard follow-up care
Receive usual care
OTHEReducational intervention
Undergo PFMT
Sponsors
National Cancer Institute (NCI)
New Mexico Cancer Research Alliance
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
30 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* History of uterine, cervical, ovarian or vulvar malignancy * Treatment free interval of \>= one year and currently have no evidence of cancer * Reports urinary incontinence based on screening questionnaire * Must have a stable address for the three month period
Exclusion criteria
* Current clinical evidence of urinary tract infection * Within three months of failed surgery for urinary incontinence * Planned surgery for urinary incontinence in the next three months * Presence of neurologic condition that may impact bladder symptoms such as multiple sclerosis, stroke * Pregnancy
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Improvement in the Patient Global Impression of Improvement (PGI-I) rating | 12 weeks | Fisher's exact test will be used to test whether the chance of success is identical for the two groups (intervention vs. control). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Changes in the Incontinence Severity Index (ISI) score | Baseline to 3 months | The Brinks scale will be used by the trainers for the treatment group follow-up to evaluate the adequacy of the contractions in a qualitative manner. A two sample t-test on the within individual differences will be used. A non-parametric Mann-Whitney test will be used if the sample differences are non-normally distributed. |
| Changes in Urinary Distress Inventory (UDI) | Baseline to 3 months | The Brinks scale will be used by the trainers for the treatment group follow-up to evaluate the adequacy of the contractions in a qualitative manner. A two sample t-test on the within individual differences will be used. A non-parametric Mann-Whitney test will be used if the sample differences are non-normally distributed. |
| Changes in Incontinence Impact Questionnaire (IIQ), which measures the impact of urinary incontinence on quality of life | Baseline to 3 months | The Brinks scale will be used by the trainers for the treatment group follow-up to evaluate the adequacy of the contractions in a qualitative manner. A two sample t-test on the within individual differences will be used. A non-parametric Mann-Whitney test will be used if the sample differences are non-normally distributed. |
Countries
United States
Outcome results
None listed