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Overactive BladderPhase 4SQUARE PDNCT07187466

Behavioral and/or Mirabegron to Treat Urinary Symptoms in Parkinson Disease

A Phase 4 study testing mirabegron and Exercise-based behavioral therapy in people with Overactive Bladder and Parkinson Disease, run by VA Office of Research and Development at 3 sites in United States.

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Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record

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Trial summary

The purpose of this study is to learn about different treatments for overactive bladder symptoms in Parkinson's Disease. The investigators want to find out if people who do not respond to one treatment (either behavioral or drug treatment) will respond to combined treatment. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Overactive Bladder, Parkinson Disease
What is being tested?
mirabegron and Exercise-based behavioral therapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
146 participants
Where
3 sitesUnited States
Study dates
21 Oct 2026to 30 Jun 2030
Phase
Phase 4

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Clinical diagnosis of Parkinson's Disease (PD) determined by a board-certified neurologist with specialty training in movement disorders
  • An ICIQ-OAB Symptom Score of 7 or higher, which indicates clinically significant symptoms of OAB, defined as presence of urinary urgency with or without urgency incontinence usually with increased daytime frequency and nocturia in the absence of infection or other obvious pathology

Who cannot join

  • Significant cognitive impairment, as indicated by a Montreal Cognitive Assessment (MoCA) score of < 18 or a telephone-MoCA score < 13, which is the recommended diagnostic cut point for dementia in PD.
  • Previous intensive pelvic floor muscle exercise training
  • Clinically significant depression as measured by a Geriatric Depression Scale-Short Form score of 10 or higher which could affect motivation to fully engage in the intervention
  • Use of an indwelling urinary catheter
  • Post-void residual urine measurement by bladder ultrasound of > 150 mL
  • Severe uterine prolapse past the vaginal introitus
Show all 19Show fewer
  • Poorly controlled diabetes defined by a hemoglobin A1c (HgbA1c) of >9.0% within the last 3 months. Participants with poorly controlled diabetes will be offered enrollment if the OAB symptoms persist after improvement in diabetes control
  • Chronic renal failure and on hemodialysis
  • Genitourinary cancer with ongoing surgical or external beam radiation treatment
  • Previous artificial urinary sphincter, sling procedure or implanted sacral neuromodulation device
  • History of bladder-injection of botulinum toxin in the last 12 months
  • Any unstable health condition expected to result in hospitalization or death within in the next 3 months as determined by principal investigator.
  • Hypersensitivity to drug class
  • Contraindication to the study drug (mirabegron) including history of acute urinary retention requiring catheterization
  • Current use of a bladder relaxant - permitted to enroll after one-week washout
  • Hematuria on microscopic examination in the absence of infection. A urologic consultation will be recommended, and enrollment will depend on clearance by a urologist and agreement by the site PI that entry into the treatment protocol is not contraindicated
  • If on diuretic, dose should be stable for at least 4 weeks
  • If taking an alpha-blocker, dose should be stable for at least 4 weeks
  • If taking dutasteride or finasteride, dose should be stable for at least 6 months

Trial locations and contacts

3 sites in 1 country. Contact the study team or a site near you to ask about taking part.

United States3 sites
  • Atlanta VA Medical and Rehab Center, Decatur, GA

    Decatur, Georgia, 30033-4004

    Taressa Sergent, (404) 321-1611 ext. 5023, Taressa.Sergent@va.gov

    Elizabeth Camille Vaughan, MD MS

  • Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA

    Philadelphia, Pennsylvania, 19104-4551

    James F Morley, MD, 215-823-5934, james.morley@va.gov

  • VA Salt Lake City Health Care System, Salt Lake City, UT

    Salt Lake City, Utah, 84148-0001

    Alayne Markland, DO, alayne.markland@va.gov

Other trials in United States

About this study

Official title: Sequential Multiple Assignment Randomized Trial to Treat Urinary Symptoms in Parkinson Disease

The purpose of this study is to learn about different treatments for overactive bladder symptoms in Parkinson's Disease. The investigators want to find out if people who do not respond to one treatment (either behavioral or drug treatment) will respond to combined treatment. The investigators also want to find out what factors influence whether someone responds to the treatments.

Read the detailed description

While Parkinson's Disease (PD) is often characterized by the motor symptoms of the disease (tremor, bradykinesia, rigidity), non-motor symptoms such as urinary symptoms correlate more closely with impaired well-being as the disease progresses. The urinary symptoms of overactive bladder (OAB), including urgency, frequency, and nocturia, with or without urinary incontinence, are the most common urinary symptoms of PD. Because OAB symptoms, such as incontinence and nocturia, are associated with falls (a cause of increased mortality in PD), spouse/caregiver stress, and, ultimately institutionalization, it is critical that the investigators optimize the care of urinary symptoms for Veterans with PD. In the non-PD population, pelvic floor muscle contractions diminish bladder muscle contraction and recent evidence demonstrates that behavioral training with pelvic floor muscle exercises improves the cortical integration of bladder afferent signals. Because of its effectiveness compared to drugs, pelvic floor muscle exercise-based behavioral therapy is recommended first-line in men and women without PD who have OAB. Pelvic floor muscle exercise-based behavioral therapy for urinary symptoms requires individuals to learn a motor skill and implement an adaptive behavioral strategy incorporating pelvic floor muscle contraction to delay the need to void when urgency strikes. The PI's research group demonstrated the feasibility and preliminary efficacy of pelvic floor muscle exercise-based behavioral therapy to treat urgency incontinence in adults with PD. However, the most recent clinical guidelines for the treatment of urinary symptoms in PD recommend treatment with anticholinergic drugs and mention the potential option for noradrenergic bladder relaxants. While some anticholinergic drugs are effective in reducing symptoms of OAB, it is important to note that there is a glaring lack of an empirical evidence base to promote these drugs in the setting of PD given that they add to the anticholinergic burden of antiparkinsonian therapy and may worsen the cognitive and autonomic burdens of the illness. Noradrenergic bladder relaxants may have a more favorable side effect profile; however, the evidence for efficacy in PD is minimal. Therefore, randomized controlled trials (RCTs) are needed to optimize treatment paradigms for urinary symptoms in PD. The investigators' preliminary studies suggest adults with PD and mild cognitive dysfunction can successfully implement behavioral therapy for urinary symptoms. However, in the investigators' most recent VA-funded, multisite trial, 50% of participants reported a clinically significant reduction in urinary symptoms after treatment with either behavioral or drug treatment. Additional research using a Sequential Multiple Assignment Randomized Trial (SMART) design offers an efficient strategy to understand both intervention and patient factors that will inform an individualized treatment plan. With a SMART design, Aim 1 will determine if non-responders to behavioral or drug treatment (expected to be 50% of population) demonstrate a clinically significant response to combination behavior and drug treatment compared to a single treatment approach. In Aim 2, the investigators will determine patient factors that influence optimized treatment of urinary symptoms in Veterans with PD.

Being tested
mirabegron, Exercise-based behavioral therapy
Keywords
Urinary Bladder, Overactive, Parkinson Disease
Medical subject headings
Urinary Bladder, Overactive, Parkinson Disease

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • mirabegronDrug

    Also called Myrbetriq

    Mirabegron is a beta-3-agonist, which acts upon the noradrenergic system and avoids the cognitive and gastrointestinal side effects of anticholinergic bladder relaxants.

  • Exercise-based behavioral therapyBehavioural

    The exercise-based behavioral therapy is a comprehensive training program administered individually by a trained nurse practitioner interventionist to address urinary incontinence and other lower urinary tract symptoms.

Study groups in NCT07187466
Study groupRoleWhat they receive
Drug Therapy GroupActive comparatorParticipants who are randomized to drug therapy will receive mirabegron 25mg at visit 2 (randomization visit).
Receives: Drug: mirabegron
Behavioral Therapy GroupActive comparatorParticipants who are randomized to exercise-based behavioral therapy will receive a comprehensive training program administered individually by a trained nurse practitioner interventionist to address urinary incontinence and other lower urinary tract symptoms.
Receives: Behavioral: Exercise-based behavioral therapy
Combined Drug and Behavioral Therapy GroupActive comparatorAt 6 weeks post-randomization, participants will complete the ICIQ-OAB questionnaire. Participants reporting less than 3 points reduction will be re-randomized to either continue their initial treatment assignment or receive combination therapy by adding the alternate treatment strategy, thus participants initially treated with mirabegron will add behavioral therapy and participants initially treated with behavioral therapy will add mirabegron.
Receives: Drug: mirabegron; Behavioral: Exercise-based behavioral therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. ICIQ-OAB

    The primary outcome measure at 12 weeks will be urinary symptom severity as measured by the International Consultation on Incontinence Questionnaire-Overactive Bladder module (ICIQ-OAB). Scores range from 0 to 16 with higher scores indicating worse symptom frequency. The symptom score will be collected at 3 time points during the study: baseline, 6-weeks, and 12-weeks.

    Measured: baseline, 6-weeks, and 12-weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Sep 2025
  2. Study start21 Oct 2026 (estimated)
  3. Primary completion31 Mar 2030 (estimated)
  4. Study completion30 Jun 2030 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Sequential
Model description
Sequential Multiple Assignment Randomized Trial (SMART) design offers an efficient strategy to understand both intervention and patient factors that will inform an individualized treatment plan. With a SMART design, Aim 1 will determine if non-responders to behavioral or drug treatment (expected to be 50% of population) demonstrate a clinically significant response to combination behavior and drug treatment compared to a single treatment approach. In Aim 2, the investigators will determine patient factors that influence optimized treatment of urinary symptoms in Veterans with PD.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
146 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07187466
Sponsor's protocol ID
RRD6-001-24W
Other IDs
1I01RD000466-01A2
Acronym
SQUARE PD
Status last verified
Oct 2026
First submitted
18 Sep 2025
Last updated
19 Oct 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: Final data sets underlying publications resulting from the proposed research will be shared outside VA through a de-identified, anonymized Dataset under a written agreement that adheres to any applicable Informed Consent provisions and prohibits the recipient from identifying or re-identifying (or taking steps to identify or re-identify) any individual whose data are included in the dataset.

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