- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02549729
Effect of the Pelvic Floor Training in Postmenopausal Women With or Without Hormonal Therapy
Effect of the Pelvic Floor Training on Pelvic Floor Muscle Strength in Postmenopausal Women With or Without Hormonal Therapy: A Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The climacteric period is marked by the decline of estrogens and androgens which represents negative effect on the urogenital system and may present, as a consequence, pelvic floor muscles (PFM) dysfunction and urinary incontinence (UI). The pelvic floor muscles training (PFMT) and hormone therapy (HT) could result in a significant increase in muscle mass with functional improvement and consequent decrease in complaints of urine loss. The aim of this study is to evaluate the effect of PFMT on muscle function, in the presence of UI, severity and impact on quality of life in postmenopausal women with or without HT.
The variable sexual function was abandoned due to the fact that the majority of the women do not presented active sexual life, which is a criteria to answer the questionnaire Index of Female Sexual Function (IFSF), or did not agree to answer the questionnaire. The anxiety scale was also abandoned because it was a tool to assess sexual function in a broader way.
This is a randomized controlled trial. Postmenopausal women will be divided into 4 groups:
- Group 1- without exercise and without HT
- Group 2 - with exercise and without HT
- Group 3 - without exercise and with HT
- Group 4 - with exercise and HT
Women will be evaluated at baseline and up to 12 weeks. The evaluations of the PFM function will be accomplished through the use of vaginal palpation using the Modified Oxford Scale (MOS) and perineometry. The International Consultation on Incontinence Questionnaire- Short Form (ICIQ - SF) will be used to assess reports of UI, quality of life will be evaluated by the SF36 (Medical Outcomes Study 36 - Item Short - Form Health Survey).
The electromyography was not performed because during the collection of data from the pilot sample there was an excess of outcome measures which made the patients' adhesion unfeasible.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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São Paulo
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Ribeirão Preto, São Paulo, Brazil
- School Healthy Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Postmenopausal women with a maximum of ten years of menopause.
- It is considered menopausal cessation of menstrual cycles for more than twelve months (WHO).
- To be included women must have the ability to contract the pelvic floor muscle (PFM) and have never done PFM training.
Exclusion Criteria:
- Women with diabetes mellitus, thyroid disease, hyperprolactinemia, genital prolapse (above grade 1), neuropathy and vasculopathy.
- Those who are intolerant (pain, allergy gel or latex condom or other discomfort) to PFM function evaluation and those that deny answer the questionnaires during the protocol.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control
Control group not using hormonal replacement therapy will not receive supervised pelvic floor muscle training.
This group will be assessed at baseline and up to 12 weeks.
For ethics reason at the end of the study women of the control group will be invited to receive the pelvic floor muscle training program.
However, this will not be part of the study.
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Experimental: Exercise
Experimental group not using hormonal replacement therapy will receive supervised pelvic floor muscle training.
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Women will be instructed to perform pelvic floor muscle training daily at home 4 sets of 10 maximum perceived voluntary contraction of the pelvic floor muscle sustained for 6 seconds followed by 5 flick voluntary contraction of the pelvic floor muscle.
The 4 sets will be performed in 4 different positions (supine, all four, sit and standing).
Twice a week they will receive a supervised session using the same protocol described above.
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|
No Intervention: Hormone Therapy
Experimental group using hormonal replacement therapy will not receive supervised pelvic floor muscle training.
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Experimental: Exercise and Hormone Therapy
Experimental group using hormonal replacement therapy will receive supervised pelvic floor muscle training.
|
Women will be instructed to perform pelvic floor muscle training daily at home 4 sets of 10 maximum perceived voluntary contraction of the pelvic floor muscle sustained for 6 seconds followed by 5 flick voluntary contraction of the pelvic floor muscle.
The 4 sets will be performed in 4 different positions (supine, all four, sit and standing).
Twice a week they will receive a supervised session using the same protocol described above.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Change in Pelvic floor muscle function, evaluated by Perineometry, up to 12 weeks.
Time Frame: Baseline measurement of pelvic floor muscle function, and up to 12 weeks. Control group will be evaluated at baseline and up to 12 weeks.
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Baseline measurement of pelvic floor muscle function, and up to 12 weeks. Control group will be evaluated at baseline and up to 12 weeks.
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Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1.076.422
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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