ClinicalTrials.gg
Active, not recruitingNCT05604222SLABUpdated Aug 10, 2026

Effect of Behavioral Sleep Intervention on Lower Urinary Tract Symptoms in Older Women

A Phase 4 interventional study of Mirabegron 50 MG and Brief Behavioral Treatment for Insomnia in Urgency Urinary Incontinence and Nocturia, sponsored by Shachi Tyagi. Active, not recruiting at 1 site in United States. Open to female participants aged 60 Years and older. Per ClinicalTrials.gov, last updated 2026-08-10.

Sponsored by Shachi Tyagi · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
60 Years and older
Sex
Female
01

Study summary

Urgency urinary incontinence (UUI) is common in older people and vastly reduces quality of life, yet the cause and mechanism of disease are not well understood. This study will investigate the role of adding behavioral sleep intervention to the standard pharmacotherapy in treatment of UUI among older adults, and the brain mechanisms involved in continence by evaluating brain changes. This will expand the current knowledge of how the sleep affects bladder control, and better characterize the brain mechanisms in maintaining continence.

Read the detailed description

Urgency urinary incontinence (UUI), a form of overactive bladder (OAB), is prevalent (36% of women over age 65), morbid and costly ($83 billion/year), and treatment is problematic. Current treatment is largely bladder centric has limited efficacy,and adherence rates fade to 21% at 12 months. The researchers believe that a complimentary approach, one that also addresses etiology beyond the bladder may enhance treatment success. Up to 50% of older adults complain of poor sleep and nighttime bladder symptoms (nocturia) are considered the major cause. However, the relationship between sleep and the bladder is complex and bidirectional. Poor sleep not only exacerbates daytime lower urinary tract symptoms (LUTS), but can also cause these, increasing the risk of LUTS by up to 55% over 5 years. Sleep disruption increases anxiety and impairs daytime attention, both of which affect bladder control. Consistent with findings in anxiety disorders and attention control, poor sleep is linked to media prefrontal cortex (mPFC) hypoactivity, a region the investigators have identified as key to executive control of voiding and to therapeutic response to biofeedback-assisted pelvic floor muscle therapy. Hence, the investigators posit that enhanced mPFC function through improved sleep might ameliorate bladder control. Despite evidence of a bidirectional relationship, the impact of sleep treatment on UUI has never been assessed. The researchers prior study demonstrated that improving sleep using Brief Behavioral Treatment of Insomnia (BBTI), a simple intervention for insomnia, improved both sleep and nocturia in older adults, yet its impact on UUI and mechanism of action is not known. Our exploratory analysis of sleep and voiding data from 20 older adults with UUI and nocturia showed that with behavioral sleep intervention alone, 24-hour UUI episodes decreased with prolongation of uninterrupted sleep before the first awakening to void (r=-0.50, p=0.02), and increased proportion of deep sleep (r=-0.56, p=0.01). Hence, the researchers postulate that addressing sleep in patients with UUI and nocturia may further potentiate bladder-focused UUI treatment. The efficacy of mirabegron, a β3- adrenoceptor agonist is comparable to first-line antimuscarinic pharmacotherapy for UUI, with fewer side effects, but it has only a modest effect on nocturia. Although these drugs show statistically significant improvement in LUTS, drug compliance remains poor secondary to modest perceived clinical benefit. The researchers central hypothesis is that comorbid insomnia contributes to poor therapeutic response for UUI and concurrent insomnia treatment will improve outcomes. Specifically, addition of BBTI to drug therapy will improve sleep, nocturia, and daytime LUTS, likely mediated by improvement of mPFC function.

The researchers propose an 8-week randomized controlled trial of mirabegron+BBTI vs. mirabegron alone for UUI in 100 women (aged ≥60), assessing both clinical and neural effects of treatment. The researchers will also assess durability of the combination therapy at 6 months. This design encompasses the role of sleep in OAB treatment, insight into the central and peripheral effects of mirabegron and BBTI, and response durability.

02

Conditions studied

  • Urgency Urinary Incontinence
  • Nocturia

Browse trials for

03

In context

Nocturia

134 studies on the registry are indexed under Nocturia; 22 are open to participants now.

This study's planned enrollment of 120 is above the median of 71 across 108 interventional studies indexed under Nocturia.

Browse Nocturia studies →

Lead sponsor

This is the only study on the registry with Shachi Tyagi as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
60 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • ambulatory women aged 60+ years
  • urgency incontinence or urge-predominant mixed incontinence (able to differentiate between stress symptoms-cough, laugh, exercise-and leakage following the sudden onset of a strong urge to void that is difficult to defer during questioning on telephone screening) occurring at least five times weekly for ≥ 3 months despite treatment for reversible causes
  • nocturia ≥2 each night
  • subjects with current or previous use of anticholinergic medications will be considered for the study if willing to go through a of at least 4 weeks of duration

Exclusion criteria

Exclusion Criteria:

  • to any of the drugs used (e.g., mirabegron, prophylactic antibiotics)
  • cognitive impairment (MOCA score \<24 or inability to accurately complete a voiding diary, perform a 24-hour pad test, reliably take daily medication, or comply with fMRI testing)
  • prior treatment with intradetrusor onabotulinum toxin or sacral neuromodulation.
  • spinal cord injury; history of pelvic irradiation, advanced uterine or bladder cancer; multiple sclerosis
  • urethral obstruction; urinary retention [PVR >200 ml]
  • interstitial cystitis; artificial sphincter implant
  • medical instability or expected change in medication during the study
  • conditions that preclude fMRI testing, such as history of claustrophobia, history or suspicion of implanted metal or electronic object
  • requirement for intravenous antibiotics for bacterial endocarditis prophylaxis or presence of multiple allergies to the antibiotics available in our protocol
  • chronic or recurrent bowel issues, e.g. IBS, colitis, fecal incontinence
  • known allergy to study medication or interaction with current medications
  • severe uncontrolled hypertension >180 mmHg systolic or >100 mmHg diastolic
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Washout period

A planned gap after a treatment, so that its effects can lessen before the study treatment or a study assessment. Ask the study team and the doctor who prescribed it before changing any medicine.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    Mirabegron

    Mirabegron for 8 weeks

    Drug: Mirabegron 50 MG

  • Experimental
    Mirabegron plus Brief Behavioral Treatment for Insomnia (BBTI)

    Mirabegron for 8 weeks and a 4 week behavioral intervention for insomnia

    Drug: Mirabegron 50 MG · Behavioral: Brief Behavioral Treatment for Insomnia

Interventions

  • Medication to treat overactive bladder

    Also known as: Myrbetriq

  • BehavioralBrief Behavioral Treatment for Insomnia

    A behavioral intervention for insomnia

    Also known as: BBTI

06

What researchers measure

Primary outcomes

  1. Incontinence episodes

    The number of incontinence episodes

    Time frame: Baseline to 8 weeks

Secondary outcomes

  1. Nocturia episodes

    The number of nocturia episodes

    Time frame: Baseline to 8 weeks

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Yes — All of the individual participant data collected during the trial, after deidentification may be shared with other researchers.

Supporting information: Study protocol, Statistical analysis plan, Informed consent form, Clinical study report

Time frame: Following publication, no end date

Access criteria: Any purpose

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05604222
Lead sponsor
Shachi Tyagi
Responsible party
Shachi Tyagi (Assistant Professor of Medicine, University of Pittsburgh) — Sponsor-investigator
First posted
Nov 3, 2022
Start date
Mar 5, 2023
Primary completion
Jun 30, 2026
Completion
Mar 31, 2027 (estimated)
Last update
Aug 10, 2026

Study contacts

Shachi Tyagi, MD
principal investigator · University of Pittsburgh

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion