- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03883724
Impact of Behavioral Treatment of Insomnia on Nighttime Urine Production
Study Overview
Status
Intervention / Treatment
Detailed Description
Prevalent, morbid, and costly ($61 billion/year in 2012), nocturia is a major problem, especially for older adults. It increases the risk of falls, fractures, depression, nursing home placement, and death. Yet management of nocturia remains inadequate. Most behavior and pharmacotherapies for nocturia focus on bladder-related etiologies, and it's most prevalent attribute nocturnal polyuria (NP), or increased urine production during sleep remains poorly understood and inadequately treated with little advancement over the last 50 years. Disruption of diurnal excretory pattern, with higher nighttime urine production is common in older adults. While studies in young adults show that sleep plays a critical role in regulating nighttime urine production, among older adults the role of poor sleep in NP is under-investigated.
Urine production follows a circadian pattern in which transition from wake to sleep is followed by a pronounced decrease in excretion of water, electrolytes and other osmotically active substances. Studies in young population have established that physiological urine production follows a circadian rhythm, which is regulated by diurnal variation in secretion of hormones controlling water and salt excretion such as arginine vasopressin, renin-angiotensin-aldosterone system, and atrial natriuretic peptide. Sleep deprivation blunts nocturnal surge of these hormones and consequently alter water and salt excretion thereby increase nighttime urine volume leading to NP.
Recent evidence suggests that poor sleep quality, frequent sleep interruptions especially in the first part of the night and shorter duration of first uninterrupted sleep period are associated with NP but its pathophysiology is not fully understood. Additionally, among older adults with poor sleep, the investigators have shown that a behavioral intervention directed solely towards sleep (BBTI- brief behavioral treatment of insomnia an efficacious multimodal behavioral treatment for insomnia) not only improves sleep, but also nocturia. Hence, the investigators postulate that sleep interruptions in the first part of the sleep impacts the hormonal regulation of nighttime urine production causing NP. In addition, the investigators postulate that interventions to prolong the first uninterrupted sleep period will decrease NP and hence nocturia.
The, aims of the present proposal are to: 1) examine the impact of BBTI on duration of the first of uninterrupted sleep period and NP in elderly with nocturia; and 2) establish NP and duration of first uninterrupted sleep as mechanisms by which BBTI impacts nocturia. The investigators' hypothesis is that BBTI improves nocturia not only by improving sleep, (and specifically, duration of the first uninterrupted sleep period), but also by decreasing NP.
To accomplish these goals the investigators will recruit 60 community dwelling adults (aged >65) with nocturia and NP. Sleep will be assessed subjectively with the Insomnia Severity Index and objectively by 7-day sleep diary and wrist actigraph. Concurrently the investigators will collect 3-day bladder diary data to document their voiding pattern and volume during day and night. Participants will be randomized to receive the 4-week behavioral sleep intervention BBTI by a trained therapist or an information control intervention. The participants will repeat the study measures post-intervention.
The study results will provide important insights into shared pathological mechanisms underlying poor sleep, nocturia and nighttime urine production.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Pennsylvania
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Pittsburgh, Pennsylvania, United States, 15213
- University of Pittsburgh
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- ambulatory and functionally-independent community-dwelling men and women
- aged 65 years, or more
- with nocturia ≥2/night
- poor sleep because of frequent awakenings
Exclusion Criteria:
- Unstable or acute medical or central nervous system conditions
- Untreated, current, severe psychiatric condition
- Untreated, current, severe overactive bladder syndrome
- Post void residual > 30ml
- Sleep apnea with AHI≥15
- Currently diagnosed and/or treated Obstructive Sleep Apnea, Restless Legs Syndrome, parasomnia
- Congestive heart failure, by exam or Beta natriuretic peptide (BNP)> 30 pmol/L
- Chronic kidney disease, stage III-V (eGFR<50)
- >14 alcohol drinks per week
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Brief behavioral treatment for insomnia
This group will undergo behavioral intervention proven to improve sleep among older adults: brief behavioral treatment for insomnia
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The BBTI consists of a 45- to 60-minute individual intervention session followed by a 30-minute follow-up session 2 weeks later and 20-minute telephone calls after 1 and 3 weeks.
The brief behavioral treatment component will focus on four behaviors that promote sleep through homeostatic, circadian, or association mechanisms.
50 These four interventions are simple to conceptualize and implement, and constitute the core of efficacious multi-modal behavioral treatments for insomnia.
|
|
Other: Information-only control
This group is called information-only control.
They will be provided sleep-related information.
They will also view a video content of which overlap substantially with BBTI but without individualized behavioral instructions.
|
The IC condition is intended to emulate the behavioral treatment information generally to available patients.
It includes instructions to review hand out on healthy sleep practices.
We will also use patient education videos on insomnia developed locally and widely used in clinical research.
The content of these videos overlap substantially with BBTI but without individualized behavioral instructions.
Two weeks later, IC participants will receive a 10-minute follow-up telephone call to encourage continued participation.
Participants will be referred to the brochures for specific sleep-related questions.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Nocturnal Polyuria Index
Time Frame: change from baseline nocturnal polyuria index at 4 weeks
|
Nocturnal Polyuria Index (NPI) is the percentage of 24-hour urine production excreted at night.
It is measured using 3-day bladder diary that participants will complete pre- and post-intervention in which the participants document the time and volume of each void during the day and night for 3 days.
NPI is calculated using a) nocturnal urine volume (determined by adding the volume of all voids between the times marked in the bladder diary as going to bed with the intent of sleeping and the first awakening to void.
The first void after waking is included in the nighttime urine volume), and b) 24-hour urine volume.
NPI is calculated as: nocturnal urine volume /24-hour urine volume
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change from baseline nocturnal polyuria index at 4 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Nocturia
Time Frame: change from baseline nocturia episodes each night at 4 weeks
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Nocturia=number of awakenings to void each night
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change from baseline nocturia episodes each night at 4 weeks
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Change in Duration of Uninterrupted Sleep
Time Frame: Change from baseline duration of uninterrupted sleep at 4 weeks
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Duration of uninterrupted sleep is the first uninterrupted sleep period before first awakening to void
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Change from baseline duration of uninterrupted sleep at 4 weeks
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Shachi Tyagi, MD, MS, University of Pittsburgh
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- PRO18100572
- R21AG060292 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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