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"The Effects of Caffeine on Overactive Bladder Symptoms and Mental Health in Postmenopausal Women"

Primary Purpose

Overactive Bladder, Caffeine, Menopause

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
400 mg of caffeine/day (Two 200mg pills/day)
200 mg of caffeine/day (One 200mg pill and one placebo pill)
Two placebo pills/day
Sponsored by
Loma Linda University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Overactive Bladder

Eligibility Criteria

58 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Low to moderate coffee drinkers (between 1-3 cups/day, or 50-450mg caffeine/d)
  • Able to communicate and read in English
  • 58 years of age or older
  • Post-menopausal

Exclusion Criteria:

  • Excessive coffee drinkers (>450 mg/d)
  • Individual who do not regularly consume caffeine
  • Uncontrolled hypertension
  • Vaginal pain
  • Chronic pelvic pain/ Interstitial cystitis
  • Pre- or perimenopausal

Sites / Locations

  • Department of Urology, Loma Linda University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

400 mg of caffeine/day (Two 200mg pills/day)

200 mg of caffeine/day (One 200mg pill and one placebo pill)

Two placebo pills/day

Arm Description

One phase of treatment will have participants consume two 200 mg-caffeine pills day (total of 400 mg of caffeine/ d) for 7 days.

This arm will receive one 200 mg caffeine pill and one sugar pill (placebo pill)

This arm will have participants consume two placebo pills each day.

Outcomes

Primary Outcome Measures

Change in voiding symptoms
Voiding symptoms will be measured through a composite of self-reported surveys. These surveys are the King's Health Questionnaire, Urinary Distress Inventory, Overactive Bladder Symptom Score, Overactive Bladder Questionnaire.
Change in mental health
Mental health symptoms will be measured through a composite of self-reported surveys. These surveys are the Insomnia Severity Index, Stress Quiz, Beck Anxiety Index, Beck Depression Inventory, The Positive and Negative Affect Scales, Rosenberg Self-Esteem Scale, and the International Physical Activity Questionnaire.

Secondary Outcome Measures

Full Information

First Posted
June 27, 2014
Last Updated
October 24, 2018
Sponsor
Loma Linda University
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1. Study Identification

Unique Protocol Identification Number
NCT02180048
Brief Title
"The Effects of Caffeine on Overactive Bladder Symptoms and Mental Health in Postmenopausal Women"
Official Title
"The Effects of Caffeine on Overactive Bladder Symptoms and Mental Health in Postmenopausal Women"
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Completed
Study Start Date
July 2014 (undefined)
Primary Completion Date
September 20, 2018 (Actual)
Study Completion Date
September 20, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Loma Linda University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to observe effects of caffeine on overactive bladder symptoms and wellbeing. This study looks at whether caffeine has bad effects on urinary symptoms or if lower doses of caffeine decrease the effects. The study will propose the following hypothesis: The voiding and mental health symptoms will be greatest in the high dose treatment and lowest in the placebo treatment. The low dose treatment will produce more voiding and mental health symptoms than the placebo treatment. Voiding and mental health symptoms will be mediated by hydration status of the patient which will be assessed using a Tanita Scale.
Detailed Description
Subjects will be exposed to 200 mg and 400 mg caffeine pills and placebo pills (free of caffeine). During each treatment period, participants will be required to avoid caffeine (except for the caffeine within the given treatment). The study is staged into 3 phases, which will last for 7 days each. After enrollment, participants will be asked to refrain from consuming any substances containing caffeine during the 21 days of treatment. Instead of coffee or other caffeine items, they will be exposed to caffeine in pill form. Participants will complete each treatment in a random, cross over blinded fashion. One phase of treatment will have participants consume two 200 mg-caffeine pills a day (total of 400 mg of caffeine/day), a second treatment will have participants consume one 200 mg-caffeine pill and one placebo pill a day. And the final treatment will have participants consume two placebo pills each day. Treatment phases will be assigned randomly to each participant. The participant will not know which phase they are receiving. Prior to the treatment, the participant will be asked to fill out a detailed diet log of her eating and drinking habits. Participants will also be asked a series of questions on a survey related to bladder symptoms and mental health periodically throughout the study. It will take about 30 minutes of their time to answer the questionnaires at individual time points. During the 21 days of the study period participants will be asked to self-monitor fluid intake and note any major changes of fluid intake compared to the initial intake log. They will be asked to conduct a 24-hour voiding and defecation log at two different time points within each treatment phase as well as prior to the study. 24-hour urine will be collected during each treatment phase at two different time points as well as prior to the study. Participants weight and lean body mass will be assessed in clinic using a Tanita scale at two times within each treatment phase and one time prior to the study

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overactive Bladder, Caffeine, Menopause

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
55 (Actual)

8. Arms, Groups, and Interventions

Arm Title
400 mg of caffeine/day (Two 200mg pills/day)
Arm Type
Active Comparator
Arm Description
One phase of treatment will have participants consume two 200 mg-caffeine pills day (total of 400 mg of caffeine/ d) for 7 days.
Arm Title
200 mg of caffeine/day (One 200mg pill and one placebo pill)
Arm Type
Active Comparator
Arm Description
This arm will receive one 200 mg caffeine pill and one sugar pill (placebo pill)
Arm Title
Two placebo pills/day
Arm Type
Placebo Comparator
Arm Description
This arm will have participants consume two placebo pills each day.
Intervention Type
Dietary Supplement
Intervention Name(s)
400 mg of caffeine/day (Two 200mg pills/day)
Intervention Description
One phase of treatment will have participants consume two 200 mg-caffeine pills day (total of 400 mg of caffeine/ d) for 7 days.
Intervention Type
Dietary Supplement
Intervention Name(s)
200 mg of caffeine/day (One 200mg pill and one placebo pill)
Intervention Description
This arm will receive one 200 mg caffeine pill and one sugar pill (placebo pill)
Intervention Type
Dietary Supplement
Intervention Name(s)
Two placebo pills/day
Intervention Description
This arm will have participants consume two placebo pills each day.
Primary Outcome Measure Information:
Title
Change in voiding symptoms
Description
Voiding symptoms will be measured through a composite of self-reported surveys. These surveys are the King's Health Questionnaire, Urinary Distress Inventory, Overactive Bladder Symptom Score, Overactive Bladder Questionnaire.
Time Frame
Voiding symptoms surveys will be completed 6 times throughout the 21-day trial, in addition to a baseline measurement pre-trial.
Title
Change in mental health
Description
Mental health symptoms will be measured through a composite of self-reported surveys. These surveys are the Insomnia Severity Index, Stress Quiz, Beck Anxiety Index, Beck Depression Inventory, The Positive and Negative Affect Scales, Rosenberg Self-Esteem Scale, and the International Physical Activity Questionnaire.
Time Frame
Mental health symptoms will be measured 6 times throughout the 21-day trial, as well as a baseline measure one time pre-trial.

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
58 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Low to moderate coffee drinkers (between 1-3 cups/day, or 50-450mg caffeine/d) Able to communicate and read in English 58 years of age or older Post-menopausal Exclusion Criteria: Excessive coffee drinkers (>450 mg/d) Individual who do not regularly consume caffeine Uncontrolled hypertension Vaginal pain Chronic pelvic pain/ Interstitial cystitis Pre- or perimenopausal
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrea Staack, MD
Organizational Affiliation
Loma Linda University, Urology Medical Group, Inc.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Urology, Loma Linda University
City
Loma Linda
State/Province
California
ZIP/Postal Code
92354
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
35363563
Citation
Staack A, Distelberg B, Moldovan C, Belay RE, Sabate J. The Impact of Caffeine Intake on Mental Health Symptoms in Postmenopausal Females with Overactive Bladder Symptoms: A Randomized, Double-Blind, Placebo-Controlled Trial. J Womens Health (Larchmt). 2022 Jun;31(6):819-825. doi: 10.1089/jwh.2021.0467. Epub 2022 Apr 1.
Results Reference
derived

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"The Effects of Caffeine on Overactive Bladder Symptoms and Mental Health in Postmenopausal Women"

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