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Clinical Trials/NCT01515722
NCT01515722
Completed
Not Applicable

Interventions to Enhance Medication Persistence and Compliance in Patients With Overactive Bladder : 6-month, Randomized, Open-label, Multi-center Trial

Samsung Medical Center13 sites in 1 country692 target enrollmentDecember 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Overactive Bladder
Sponsor
Samsung Medical Center
Enrollment
692
Locations
13
Primary Endpoint
Difference in the % of patients maintaining persistence between no intervention and HEI group
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Study Objectives: To explore the effectiveness of adjunctive intervention to enhance the medication compliance and persistence in patients with Overactive Bladder (OAB), thereby to improve treatment outcomes

Study Hypothesis: Health Education Intervention (HEI) can enhance the medication compliance and persistence, thereby can improve the treatment outcomes in conjunction with pharmacological therapy in OAB patients

Study Design: 6-month, randomized, open-label, multi-center trial at 13 university hospitals

Detailed Description

Treatment - Fesoterodine (Toviaz) 4 or 8mg Interventions (2 arms) - Arm 1: No intervention Patients in this arm will not be given HEI in conjunction with pharmacotherapy (Toviaz) which was developed for this trial. - Arm 2: Health education intervention (HEI) HEI will be performed by trained study coordinators with the leaflet designed for this trial composed of 4 parts. 1. Part 1: Understanding OAB Physiology of bladder Definition, symptom and prevalence of OAB OAB in a treatable condition. There are many options that may help your symptoms. Lifestyle change Medications Bladder training Pelvic floor muscle exercise 2. Part 2: Behavioral/lifestyle modification Modification of dietary habits Limit bladder irritants- caffeine (coffee, tea, coke...), juice, chemical flavors, spicy food. etc. Altering fluid intake Weight management Learn how weight can affect their condition Stop smoking Constipation management 3. Part 3: Bladder training Timed voiding- Goal is urinating every 3 or 4 hours during the day without fear of wetting accidents. Urgency suppression Pelvic muscle contraction, count backwards from 100 by 7seconds, etc Pelvic floor muscle exercise Contraction (fast and slow) and relax the muscle for a count of 3. Repeat the fast and slow contractions 10 - 15 times. Do those at least 3 times a day. 4. Part 4: Understanding antimuscarinics How the medicine works How to take it Tips that may help manage side effects- dry mouth, constipation Therapy expectations 5. HEI include 3-day voiding diary for self tracking method.

Registry
clinicaltrials.gov
Start Date
December 2010
End Date
June 2012
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Female aged ≥ 18 years with OAB symptoms for ≥ 3 months
  • The sum score of the OABSS ≥ 3 with the score of the question no.3 (urgency) ≥ 2
  • The sum score of the OAB V8 ≥ 8

Exclusion Criteria

  • Any condition that would contraindication of anticholinergic treatment
  • Symptomatic acute UTI during the run-in period
  • Diagnosed or suspected interstitial cystitis
  • Treatment with anticholinergic drugs within 12 months prior to Screening and persist over 3 months
  • Treatment within the 14 days preceding Screening, or expected to initiate treatment during the study with any other treatment for overactive bladder.
  • An indwelling catheter or practicing intermittent self-catheterization
  • Pregnant or nursing women

Outcomes

Primary Outcomes

Difference in the % of patients maintaining persistence between no intervention and HEI group

Time Frame: 6 months

Definition of "Maintaining Persistence"= a gap of ≤ 30 days between successive prescription fills

Secondary Outcomes

  • Difference in the % of patients maintaining persistence between no intervention and HEI group(1, 2 and 4 months)
  • Difference in changes in OAB symptoms between no intervention and HEI group(1, 2, 4, and 6 months)
  • Difference in the compliance rate between no intervention and HEI group(1, 2, 4 and 6 months)
  • Adverse events(1, 2, 4, and 6 months)
  • Difference in the treatment satisfaction between no intervention and HEI group(1, 2, 4, and 6 months)
  • Difference in the % of the patients with the compliance rate ≥ 80% between no intervention and HEI group(1, 2, 4, and 6 months)
  • Reasons for non-persistence(1, 2, 4, and 6 months)

Study Sites (13)

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