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A Randomized Controlled Trial of Electrical Stimulation to Treat Pelvic Floor Disorder

To Evaluate The Efficacy of Electrical Stimulation and Biofeedback Treatment for Pelvic Floor Disorder Women

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02185235
Enrollment
200
Registered
2014-07-09
Start date
2014-06-30
Completion date
2025-05-31
Last updated
2022-11-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pelvic Organ Prolapse, Incontinence

Keywords

Electrical stimulation, Biofeedback

Brief summary

Female pelvic floor disorders (PFDs) include urinary incontinence,pelvic organ prolapse (POP), and fecal incontinence-which often occur together. Pelvic floor disorders impair multiple aspects of the life quality, including the sexual function of women. Surgery became the first choice of treatment, however, and not until 1980s was the renewed interest in conservative therapies. This may be because of higher awareness among women and cost of and morbidity after surgery. The conservative treatment included pelvic floor muscle training, electrical stimulation, vaginal cones, and biofeedback. The outcome was up to 35\ 70 % improved rate as the literature before. Current guidelines recommended conservative management as a first-line therapy. However, there was no consistent consensus on this issue due to variations in stimulation parameters、adjuvant concurrent modality or duration of treatment course, and insufficient result about large and long term follow up of randomized- controlled studies. Therefore, the investigators try to conduct one randomized-controlled trial to evaluate the efficacy of conservative treatment for Pelvic floor disorder (Pelvic organ prolapse, urinary incontinence, chronic pelvic pain etc.). At the aspect of Quality of life, our studies tried to focus on the different domains of pelvic disorder and sexual quality by means of validated questionnaire more objectively.

Interventions

DEVICEElectrical Stimulation

The Chartered Society of Physiotherapy recommends the following standard for electrical devices. Frequency: 35 Hertz. Pulse width: 250µs (0.25ms). Current type: bi-phasic rectangular. Intensity: maximum tolerated. Duty-cycle: 5 seconds on/10 seconds off. Very weak muscles: 5 seconds on/15 seconds off. Treatment time: 5 minutes initially, gradually increasing to 20 minutes.

DEVICEBiofeedback

Biofeedback is a treatment technique in which people are trained to improve their health by using signals from their own bodies

First, as you are sitting or lying down, try to contract the muscles you would use to stop urinating To contract the pelvic muscles, squeeze for 3 seconds and then relax for 3 seconds. Repeat this exercise to 20 minutes each session.

Sponsors

Mackay Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients suffering from pelvic organ prolapse and/or urinary incontinence and/or fecal incontinence.

Exclusion criteria

* Patient is pregnant The patient had any major medical or psychiatric disease The patient with Metabolic medical device

Design outcomes

Primary

MeasureTime frameDescription
1-Hour Pad test of urine leakage amount (gm)Total 18 times of treatment, for 3 monthsA pad test is a tool to used to measure urine leakage amount . Pad testing can be done over a period of time to one hour. A sanitary napkin is weighed and then worn for sixty minutes, during which time the individual is asked to perform certain activities which may include: * Walking briskly for three minutes * Sitting and then standing ten to twenty times * Walking up and down stairs for one to two minutes * Picking up objects from the floor five to ten times * Coughing twelve times (at various strengths; may be repeated) * Running in place for one minute (may be repeated) The pad is then removed and weighed again to calculate the amount of urine voided.

Secondary

MeasureTime frame
Quality of life (score)Total 18 times of treatment, for 3 months

Other

MeasureTime frameDescription
Vaginal pressure (mmHg)Total 18 times of treatment, for 3 monthsUse the vaginal probe sensor to evaluate the objective level of vaginal squeezing pressure and endurance time
Urodynamics data analysisTotal 18 times of treatment, for 3 monthsUse urodyanmic examinations for evaluation of bladder function

Countries

Taiwan

Contacts

Primary ContactTsung-Hsien Su, PhD
drthsu@mail.itrip.com.tw886-25433535

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026