Summary

for females ages 18 years and up (full criteria)
healthy people welcome
at UCLA
study started
estimated completion:

Description

Summary

The overall objective of this study is to compare the efficacy of the standard monthly maintenance therapy for percutaneous tibial nerve stimulation (PTNS), to sessions as the patient needs (prn) between 2 weeks and 12 weeks, based on overactive bladder symptoms. This is study is to help determine feasibility for conducting a larger trial that is appropriately powered to provide meaningful data.

Details

Patient will be recruited from the Urogynecology clinic on the first floor of the hospital. Patients who have completed 12 weeks of PTNS therapy will be identified by the clinic nurse or nurse practitioner and then a member of the research team will approach the patient regarding involvement in the study. Patients will be asked if they would like to take part in this study and will be given the human bill of rights and well as consent forms in their preferred language (English or Spanish) if they agree to participate. Once they agree to participate, they will be asked to sign the consent forms in a private patient room.

This is a pilot study for feasibility designed as an equivalence and cost analysis study. Patients will be recruited at the 12th session of PTNS (conclusion of treatment and before maintenance therapy starts).

Patients will be from the Urogynecology clinic at Harbor UCLA Medical Center who have OAB and who have been treated with the standard 12 sessions of PTNS. Patients will be randomized to "every month PTNS maintenance" or "as needed PTNS maintenance (Q2-12 weeks)." At enrollment, questions will be read to patients in either Spanish or English based on patient's preferred language and study staff will fill out the surveys for the patient. The patient with the study staff will complete the validated questionnaires, Overactive Bladder Questionnaire (OAB-q), the Benefit, Satisfaction and Willingness to Continue the Treatment questionnaire (BSW) and the Visual analogue scale for satisfaction with treatment. Urinary symptoms will be measured by the validated Overactive Bladder Symptom Scale (OAB-SS) and a modified voiding diary. All patients will have a urine dip completed at this visit to rule out a bladder infection. Finally patients, with the help of study staff, will answer open ended questions. All of these measures will be repeated 3 months after enrollment and one year from enrollment. After the yearlong study, participants can continue treatment which will be decided by the patient and treating clinician. A cost analysis will compare the cost to patients and the cost to the clinic between the monthly PTNS maintenance group and the patient prn maintenance group. All of the above measures will be recorded at enrollment, 3 months from enrollment and 1 year from enrollment. This will be done in person with the help of the study staff at enrollment and either in person, via the phone or in writing at 3 month and 1 year follow up. No payment and no other recruitment methods will be used.

Keywords

Overactive Bladder Urinary Bladder, Overactive PTNS maintenance PTNS monthly

Eligibility

You can join if…

Open to females ages 18 years and up

  • Patients will be eligible if they have completed 12 session of PTNS treatment and agree to continue with maintenance therapy.
  • Inclusion criteria is Women >=18 years of age, Completed 12 weeks of PTNS and desire to continue,
  • Capable of giving informed consent, primary language of English or Spanish,
  • Ambulatory and able to use toilet independently without difficulty, Capable and willing to follow all study-related procedures, OAB

You CAN'T join if...

  • Exclusion criteria includes Botox® use in bladder or pelvic floor muscles within past one year,
  • Current urinary tract infection, Male, under 18 years old, non-English or Spanish speaking, patients who are unable to consent for themselves, prisoners, pregnant patients.

Location

  • Harbor UCLA Medical Center accepting new patients
    Torrance California 90509 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Los Angeles Biomedical Research Institute
ID
NCT03136601
Study Type
Interventional
Last Updated