TReating Incontinence for Underlying Mental and Physical Health

Urinary Incontinence Clinical Trial

— TRIUMPH  

Official title:

Cognitive, Urinary, and Functional Trajectories of Older Women Using Pharmacologic Treatment Strategies for Urgency Incontinence

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05362292
• Other study ID #: 21-35858
• Secondary ID: 1R01AG075471-01
• Status: Recruiting
• Phase: Phase 4
• Start date: October 4, 2022
• Est. completion date: December 28, 2026

Study information

• Verified date: December 2023
• Source: University of California, San Francisco
• Contact: Alison Huang, MD, MAS, MPhil
• Phone: 415-514-8697
• Email: alison.huang[@]ucsf.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The TRIUMPH study is a randomized, double-blinded, 3-arm, parallel-group trial designed to compare the effects of anticholinergic bladder therapy versus a) beta-3-adrenergic agonist bladder therapy and b) no bladder pharmacotherapy on cognitive, urinary, and other aging-related functional outcomes in ambulatory older women with urgency-predominant urinary incontinence and either normal or mildly impaired cognitive function at baseline.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 270
• Est. completion date: December 28, 2026
• Est. primary completion date: September 28, 2026
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 60 Years and older

Eligibility

Inclusion Criteria:

• Aged 60 years or older at the time of enrollment

• Female sex at birth, without surgical or hormonal gender re-assignment therapy

• Able to walk to the bathroom and use the toilet without assistance

• Report urinary incontinence starting at least 3 months prior to screening

• Report that at least half of incontinence episodes occur with a sudden or strong sensation of urgency

• Report 2 or more urgency incontinence episodes over a 7-day period

• Willing to provide informed consent and adhere to study procedures throughout the length of the study

Exclusion Criteria:

• Prior clinician diagnosis of dementia, or a Montreal Cognitive Assessment (MOCA) score of 17 or lower on screening cognitive evaluation

• Current use of anticholinergic, beta-3-adrenergic agonist, or other medication designed to improve urgency incontinence symptoms, or use in the past 1 month

• Initiation, discontinuation, or dose change of dementia medications (such as donepezil, galantamine, memantine, rivastigmine) in the past 1 month (but candidates on stable doses are eligible)

• Initiation, discontinuation, or dose change of other drugs with strong anticholinergic effects (based on the Beers List) in the past 1 month (but candidates on stable doses are eligible)

• Initiation, discontinuation, or dose change of other drugs that can affect urinary frequency, including diuretics, in the past 1 month (but candidates on stable doses are eligible)

• Current urinary tract infection (UTI) based on screening urinalysis and culture (but candidates can re-present for re-screening after undergoing treatment for UTI)

• History of allergy or sensitivity to either of the study medications or an ingredient in the placebo or study medication capsule

• Severe hepatic impairment (Child-Pugh score B or greater) or renal impairment (creatinine clearance <30 mL/min) as a contraindication to both study medications

• Current bladder obstruction or urinary retention (defined by symptoms suggesting difficulty emptying the bladder in addition to postvoid residual urine volume greater than 150 cc by portable bladder ultrasound)

• Uncontrolled hypertension (based on measured systolic blood pressure greater than 180 or diastolic blood pressure greater than 110 mmHg) as a contraindication to beta-3-adrenergic therapy

• Self-reported history of gastric retention, uncontrolled narrow angle glaucoma, myasthenia gravis, severe ulcerative colitis, or toxic megacolon as contraindications for anticholinergic bladder therapy

• Use of drugs with adverse interactions with one of the study medications in the past 1 month, including potent CYP3A4 inhibitors, hepatic enzyme metabolism inducers, narrow therapeutic index drugs metabolized by CYP2D6, or intention to start taking one of these medications during the study treatment period

• History of bladder surgery, invasive intra-vesical therapy, or bulk bladder injections in the past 3 months (more remote surgery will not be exclusionary), or intention to undergo one of these procedures in the study treatment period

• Use of other specialized incontinence therapy (electrostimulation, pelvic physiotherapy, formal behavioral therapy overseen by certified practitioners) in the past 3 months (more remote therapy will not be exclusionary), or intention to undergo one of these procedures in the study treatment period

• Inability to sign informed consent or complete questionnaires, interviews, or study testing in English

• Other condition that would prevent the participant from completing study procedures, in the opinion of the investigators (e.g., uncontrolled psychosis)

Related Conditions & MeSH terms

• Enuresis
• Incontinence
• Incontinence, Urge
• Incontinence, Urinary
• Overactive Bladder
• Urinary Bladder, Overactive
• Urinary Incontinence
• Urinary Incontinence, Urge

Intervention

Drug:
• Tolterodine Tartrate ER
Anticholinergic
• Mirabegron
Beta-3-adrenergic agonist
• Placebo
matching placebo pill

Locations

Country	Name	City	State
United States	Stanford University	Palo Alto	California
United States	University of California San Francisco	San Francisco	California

Sponsors (2)

Lead Sponsor	Collaborator
University of California, San Francisco	National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in composite cognitive function over 6 months (24 weeks) of treatment, using a composite cognitive score that incorporates normalized data from all domain-specific cognitive tests.	The composite cognitive score will be calculated as the average of Z-scores from the following individual cognitive tests: a) Auditory Verbal Learning Test (AVLT); b) Oral Trail Making Test (OTMT) part A; c) OTMT part B; d) Digit Span Test; and e) Digit Symbol Substitution Test (DSST). The normative mean of each cognitive test will be subtracted from each participant's component test score, and this difference will be divided by the standard deviation for the appropriate normative sample. After scores from individual tests are transformed to Z scores as a common metric based on normative data, the average Z score from all available tests will be calculated to provide a composite Z score.	Baseline to 6 months
Secondary	Change in composite cognitive function over 9 months (36 weeks), using a composite cognitive score that incorporates normalized data from all domain-specific cognitive tests.	The composite cognitive score will be calculated as the average of Z-scores from the following individual cognitive tests: a) Auditory Verbal Learning Test (AVLT); b) Oral Trail Making Test (OTMT) part A; c) OTMT part B; d) Digit Span Test; and e) Digit Symbol Substitution Test (DSST). The normative mean of each cognitive test will be subtracted from each participant's component test score, and this difference will be divided by the standard deviation for the appropriate normative sample. After scores from individual tests are transformed to Z scores as a common metric based on normative data, the average Z score from all available tests will be calculated to provide a composite Z score.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in Auditory Verbal Learning Test total learning score assessed over 6 months (24 weeks) of treatment	The Rey Auditory Verbal Learning Test (AVLT), a widely used test of immediate and delayed verbal learning with established norms in older adults and multiple alternate forms. The total learning score is the sum of words learned from trials 1-5.	Baseline to 6 months (end of treatment)
Secondary	Change in Auditory Verbal Learning Test total learning score assessed over 9 months (36 weeks).	The Rey Auditory Verbal Learning Test (AVLT), a widely used test of immediate and delayed verbal learning with established norms in older adults and multiple alternate forms. The total learning score is the sum of words learned from trials 1-5.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change Auditory Verbal Learning Test delayed free recall score over 6 months (24 weeks) of treatment.	The Rey Auditory Verbal Learning Test (AVLT), a widely used test of immediate and delayed verbal learning with established norms in older adults and multiple alternate forms. Score range of 0-15.	Baseline to 6 months (end of treatment)
Secondary	Change Auditory Verbal Learning Test delayed free recall score over 9 months (36 weeks).	The Rey Auditory Verbal Learning Test (AVLT), a widely used test of immediate and delayed verbal learning with established norms in older adults and multiple alternate forms. Score range of 0-15.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in Oral Trail Making A score over 6 months (24 weeks) of treatment.	The oral version of the Trail Making Test (OTMT), a timed measure of attention (part A) and executive function (part B) adapted from the written TMT, with established norms for participants across a wide range of ages. Range of 1-150 seconds	Baseline to 6 months (end of treatment)
Secondary	Change in Oral Trail Making A score over 9 months (36 weeks).	The oral version of the Trail Making Test (OTMT), a timed measure of attention (part A) and executive function (part B) adapted from the written TMT, with established norms for participants across a wide range of ages. Range of 1-150 seconds	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in Oral Trail Making B score over 6 months (24 weeks) of treatment.	The oral version of the Trail Making Test (OTMT), a timed measure of attention (part A) and executive function (part B) adapted from the written TMT, with established norms for participants across a wide range of ages. Range of 1-300 seconds.	Baseline to 6 months (end of treatment)
Secondary	Change in Oral Trail Making B score over 9 months (36 weeks).	The oral version of the Trail Making Test (OTMT), a timed measure of attention (part A) and executive function (part B) adapted from the written TMT, with established norms for participants across a wide range of ages. Range of 1-300 seconds.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in Digit Span reverse component (total correct trials) over 6 months (24 weeks) of treatment.	The Digit Span Reverse (total correct trials), a subtest of the Wechsler Adult Intelligence and Memory Scales, a test of attention and short-term verbal memory, with reliability across in-person and videoconference platforms. Range of 0-14.	Baseline to 6 months (end of treatment)
Secondary	Change in Digit Span reverse component (total correct trials) over 9 months (36 weeks).	The Digit Span Reverse (total correct trials), a subtest of the Wechsler Adult Intelligence and Memory Scales, a test of attention and short-term verbal memory, with reliability across in-person and videoconference platforms. Range of 0-14.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in Digit Symbol Substitution Test score over 6 months (24 weeks) of treatment.	The Digit Symbol Substitution Test (DSST), a timed, written test assessing incidental memory, visual scanning, and processing speed, in which subjects translate numbers into symbols using a key. Range of 1-133.	Baseline to 6 months (end of treatment)
Secondary	Change in Digit Symbol Substitution Test score over 9 months (36 weeks).	The Digit Symbol Substitution Test (DSST), a timed, written test assessing incidental memory, visual scanning, and processing speed, in which subjects translate numbers into symbols using a key. Range of 1-133.	Baseline 9 months (3 months after end of treatment)
Secondary	Change in frequency of urgency-type incontinence (episodes/week) over 6 months (24 weeks) of treatment.	Frequency and type of incontinence will be assessed using a standardized, 7-day voiding diary.	Baseline to 6 months (end of treatment)
Secondary	Change in frequency of urgency-type incontinence (episodes/week) over 9 months (36 weeks).	Frequency and type of incontinence will be assessed using a standardized, 7-day voiding diary.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in frequency of any-type incontinence (episodes/week) over 6 months (24 weeks) of treatment.	Frequency and type of incontinence will be assessed using a standardized, 7-day voiding diary.	Baseline to 6 months (end of treatment)
Secondary	Change in frequency of any-type incontinence (episodes/week) over 9 months (36 weeks).	Frequency and type of incontinence will be assessed using a standardized, 7-day voiding diary.	Baseline to 9 months (3 months after end of treatment)
Secondary	Resolution of urinary incontinence from baseline to 6 months (24 weeks).	Frequency and type of incontinence will be assessed using a standardized, 7-day voiding diary.	Baseline to 6 months (end of treatment)
Secondary	Resolution of urinary incontinence from baseline to 9 months (36 weeks).	Frequency and type of incontinence will be assessed using a standardized, 7-day voiding diary.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in Overactive Bladder Questionnaire Short-Form (OAB-Q SF) Symptom Bother domain score over 6 months (24 weeks) of treatment.	Bothersomeness and impact of overactive bladder symptoms (such as urgency, incontinence, and nocturia) will be assessed using the short-form of the OAB-Q, which generates both a Symptom Bother domain and a Health-Related Quality of Life domain score.	Baseline to 6 months (end of treatment)
Secondary	Change in Overactive Bladder Questionnaire Short-Form (OAB-Q SF) Symptom Bother domain score over 9 months (36 weeks).	Bothersomeness and impact of overactive bladder symptoms (such as urgency, incontinence, and nocturia) will be assessed using the short-form of the OAB-Q, which generates both a Symptom Bother domain and a Health-Related Quality of Life domain score.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in Overactive Bladder Questionnaire Short-Form (OAB-Q SF) Health-Related Quality of Life domain score over 6 months (24 weeks) of treatment.	Bothersomeness and impact of overactive bladder symptoms (such as urgency, incontinence, and nocturia) will be assessed using the short-form of the OAB-Q, which generates both a Symptom Bother domain and a Health-Related Quality of Life domain score.	Baseline to 6 months (end of treatment)
Secondary	Change in Overactive Bladder Questionnaire Short-Form (OAB-Q SF) Health-Related Quality of Life domain score over 9 months (36 weeks).	Bothersomeness and impact of overactive bladder symptoms (such as urgency, incontinence, and nocturia) will be assessed using the short-form of the OAB-Q, which generates both a Symptom Bother domain and a Health-Related Quality of Life domain score.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in global sleep quality score over 6 months (24 weeks) of treatment.	Perceived sleep quality will be assessed using the Pittsburgh Sleep Quality Index (PSQI), an 18-item validated questionnaire designed to assess sleep quality, latency, efficiency, and problems over a one-week period.	Baseline to 6 months (end of treatment)
Secondary	Change in global sleep quality score over 9 months (36 weeks).	Perceived sleep quality will be assessed using the Pittsburgh Sleep Quality Index (PSQI), an 18-item validated questionnaire designed to assess sleep quality, latency, efficiency, and problems over a one-week period.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in daytime sleepiness score over 6 months (24 weeks) of treatment.	Daytime sleepiness will be assessed using the Epworth Sleepiness Scale (ESS), an 8-item questionnaire assessing the level of general sleepiness during real life situations in order to distinguish excessive daytime sleepiness from normal daytime sleepiness.	Baseline to 6 months (end of treatment)
Secondary	Change in daytime sleepiness score over 9 months (36 weeks).	Daytime sleepiness will be assessed using the Epworth Sleepiness Scale (ESS), an 8-item questionnaire assessing the level of general sleepiness during real life situations in order to distinguish excessive daytime sleepiness from normal daytime sleepiness.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in perceived physical function over 6 months (24 weeks) of treatment.	Perceived physical function will be assessed using the PROMIS 10B Adult Physical Function Scale, a 10-item measure that assesses the extent to which daily activities are limited by function of the extremities and central regions.	Baseline to 6 months (end of treatment)
Secondary	Change in perceived physical function over 9 months (36 weeks).	Perceived physical function will be assessed using the PROMIS 10B Adult Physical Function Scale, a 10-item measure that assesses the extent to which daily activities are limited by function of the extremities and central regions.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in confidence in maintaining balance over 6 months (24 weeks) of treatment.	Confidence in maintaining balance will be assessed using the 15-item Activities Balance Confidence Scale (ABC-S), in which participants self-rate their confidence in keeping balance with performing daily living tasks.	Baseline to 6 months (end of treatment)
Secondary	Change in confidence in maintaining balance over 9 months (36 weeks).	Confidence in maintaining balance will be assessed using the 15-item Activities Balance Confidence Scale (ABC-S), in which participants self-rate their confidence in keeping balance with performing daily living tasks.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in overall physical performance over 6 months (24 weeks) of treatment.	Physical function will be directly assessed using the Short Physical Performance Battery (SPPB), involving: 1) side-by-side, semi-tandem, and tandem balance tests; 2) a 4-meter walk test; and 3) 5 chair stands, in which participants will be asked to stand up repeatedly from a standard chair to a full extended standing position.	Baseline to 6 months (end of treatment)
Secondary	Change in overall physical performance over 9 months (36 weeks).	Physical function will be directly assessed using the Short Physical Performance Battery (SPPB), involving: 1) side-by-side, semi-tandem, and tandem balance tests; 2) a 4-meter walk test; and 3) 5 chair stands, in which participants will be asked to stand up repeatedly from a standard chair to a full extended standing position.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in static balance over 6 months (24 weeks) of treatment.	Static balance will additionally be assessed by asking participants to attempt to assume a one-legged stand for 30 seconds.	Baseline to 6 months (end of treatment)
Secondary	Change in static balance from over 9 months (36 weeks).	Static balance will additionally be assessed by asking participants to attempt to assume a one-legged stand for 30 seconds.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in lower extremity strength measured by chair stand testing over 6 months (24 weeks) of treatment.	Physical strength will be assessed 30-second chair stand, by asking participants to stand up as many times as possible within 30 seconds, with higher number indicating more strength or power.	Baseline to 6 months (end of treatment)
Secondary	Change in lower extremity strength measured by chair stand testing over 9 months (36 weeks).	Physical strength will be assessed 30-second chair stand, by asking participants to stand up as many times as possible within 30 seconds, with higher number indicating more strength or power.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in depression symptoms over 6 months (24 weeks) of treatment.	Depression symptoms will be assessed using the 15-item short form of the Geriatric Depression Scale-15 (GDS-15), which assesses symptoms of depression over a 1-week period.	Baseline to 6 months (end of treatment)
Secondary	Change in depression symptoms over 9 months (36 weeks).	Depression symptoms will be assessed using the 15-item short form of the Geriatric Depression Scale-15 (GDS-15), which assesses symptoms of depression over a 1-week period.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in anxiety symptoms over 6 months (24 weeks) of treatment.	Anxiety symptoms will be assessing using the Generalized Anxiety Disorder-7 (GAD7), 7-item short form, questionnaire to assess severity of anxiety symptoms over a 2-week period.	Baseline to 6 months (end of treatment)
Secondary	Change in anxiety symptoms over 9 months (36 weeks).	Anxiety symptoms will be assessing using the Generalized Anxiety Disorder-7 (GAD7), 7-item short form, questionnaire to assess severity of anxiety symptoms over a 2-week period.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in constipation symptoms over 6 months (24 weeks) of treatment.	Symptoms of constipation as a possible side effect of anticholinergic therapy will be assessed by the 9-item PROMIS Constipation scale of the PROMIS Gastrointestinal Symptoms-Constipation Scale.	Baseline to 6 months (end of treatment)
Secondary	Change in constipation symptoms over 9 months (36 weeks).	Symptoms of constipation as a possible side effect of anticholinergic therapy will be assessed by the 9-item PROMIS Constipation scale of the PROMIS Gastrointestinal Symptoms-Constipation Scale.	Baseline to 9 months (3 months after end of treatment)
Secondary	Change in bowel incontinence symptoms over 6 months (24 weeks) of treatment.	Bowel incontinence as a syndrome that frequently overlaps with urinary incontinence will be assessed using the 4-item PROMIS Bowel Incontinence scale.	Baseline to 6 months (end of treatment)
Secondary	Change in bowel incontinence symptoms over 9 months (36 weeks).	Bowel incontinence as a syndrome that frequently overlaps with urinary incontinence will be assessed using the 4-item PROMIS Bowel Incontinence scale.	Baseline to 9 months (3 months after end of treatment)