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Perioperative Post-Prostatectomy Incontinence Home Telehealth Program (ProsTel)

Primary Purpose

Urinary Incontinence, Prostate Cancer

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Pelvic Floor Muscle Training
Perioperative Care and Wetness Management
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urinary Incontinence focused on measuring radical prostatectomy, urinary incontinence, prostate cancer, telehealth, pelvic floor muscle training

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Scheduled to undergo a radical prostatectomy for treatment of prostate cancer and enrolled at the Birmingham, Philadelphia, or Atlanta VA Medical Centers or the affiliated University Medical Centers
  • Ability to read English.
  • Internet access

Exclusion Criteria:

  • Urinary Incontinence in the 6 months prior to prostate cancer surgery (other than post-void dribbling)
  • Less than 1 week before surgery

Sites / Locations

  • Birmingham VA Medical Center
  • Atlanta VA Medical and Rehab Center, Decatur, GA
  • Philadelphia VA Medical Center, Philadelphia, PA

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Telehealth with Pelvic Floor Muscle Training

Telehealth without Pelvic Floor Muscle Training

Arm Description

Participants in this group will participate in an evidence-based pelvic floor muscle training program that has been adapted to telehealth format. Training is begun 1 month before surgery and continued 2 months after surgery. Content is accessed in 10-minute sessions on a secure website - daily preoperatively and for the first 2 months post-operatively, then weekly until 6 months post-operatively. In addition to the pelvic floor muscle training, content will also include general perioperative care; wetness, odor and skin care management; and outcome measures.

Participants in this group will receive a telehealth program that includes include general perioperative care; wetness, odor and skin care management; and outcome measures. The program is begun 3 weeks before surgery and continued 2 months after surgery. Content is accessed in 10-minute sessions on a secure website - daily preoperatively and for the first 2 months post-operatively, then weekly until 6 months post-operatively.

Outcomes

Primary Outcome Measures

Time to Continence
Time to continence was based on the time point at which participants reported no urinary incontinence on the International Consultation on Incontinence (ICI) Questionnaire-Urinary Incontinence Short Form (ICIQ-UI SF). ICIQ-UI SF is one of a series of ICI questionnaires that have been meticulously developed and tested. The ICIQ-UI SF is a brief (4 items), reliable (Cronbach's alpha = 0.95), questionnaire that quantifies both symptom burden and impact of incontinence and has been validated in men and women. It was administered weekly during the 6 months after surgery. Scores range from 0-21; higher scores indicate worse condition.

Secondary Outcome Measures

International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form (ICIQ-UI SF) Total Score
International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form total score. Scores range from 0-21; higher scores indicate worse condition.
Expanded Prostate Cancer Index Urinary Incontinence Subscale (EPIC-UI)
This measure, validated as a stand-alone assessment, consists of 4 questions from the full Expanded Prostate Cancer Index (EPIC), a health-related quality of life assessment tool. The EPIC was developed based on advice from an expert panel and prostate cancer survivors, expanding the 20-item University of California - Los Angeles Prostate Cancer Index. Scores range from 0-100; higher scores indicate worse condition.
Incontinence Impact Questionnaire - Short Form (IIQ-SF)
This measure, validated in men with post-prostatectomy incontinence, measures the impact of incontinence on regular activities. It is a condition-specific quality of life measure that has been widely used in incontinence clinical trials. There are seven items. Response options are: "not at all," "slightly," "moderately," "greatly." Scores range from 0-100; higher scores indicate greater impact.
International Prostate Symptom Scale - Quality of Life Question
Validated single question: "If you were to spend the rest of your life with your urinary problem the way it is now, how would you feel about that?" Response options: delighted, pleased, mostly satisfied, mixed (about equally satisfied and dissatisfied), mostly dissatisfied, unhappy, terrible.
Patient Satisfaction Question (PSQ)
Patient's rating of satisfaction (Completely satisfied, Somewhat satisfied, Not at all satisfied)
Estimated Percent Improvement (EPI)
Participant self-report of perceived percent improvement from 0% to 100%
Global Perception of Improvement (GPI)
Participant's global perception of their improvement (Much better, Better, About the same, Worse, Much worse)
How Disturbing is Urine Leakage
Single quality of life question: "How disturbing is the urine leakage problem to you?" (not at all, somewhat, or extremely disturbing)
Activity Restriction
Single quality of life question: "How much does leakage of urine restrict your activities?" (not at all, some of the time, most of the time, all of the time).
Return to Work
Single quality of life question: "Have you been able to return to work since your surgery?" (yes, no, retired or disabled)
Resumption of Normal Activity
Single quality of life question: "Have you been able to resume your usual activities since your surgery?" (yes, no)

Full Information

First Posted
October 4, 2013
Last Updated
July 14, 2021
Sponsor
VA Office of Research and Development
Collaborators
Emory University, University of Pennsylvania, University of Alabama at Birmingham
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1. Study Identification

Unique Protocol Identification Number
NCT01960998
Brief Title
Perioperative Post-Prostatectomy Incontinence Home Telehealth Program
Acronym
ProsTel
Official Title
Perioperative Post-Prostatectomy Incontinence Home Telehealth Program
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
August 11, 2014 (Actual)
Primary Completion Date
September 30, 2019 (Actual)
Study Completion Date
September 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development
Collaborators
Emory University, University of Pennsylvania, University of Alabama at Birmingham

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Many men develop urine leakage after prostate cancer surgery. Usually it is temporary, but pelvic floor muscle training and exercise (including urine control strategies) have been shown to reduce the time to regaining urine control. This study tests an evidence-based, pelvic floor muscle training program that has been adapted to telehealth format and pilot tested in a VA-funded pilot/developmental trial. Training is begun 1-4 weeks before surgery and continued 6 months after surgery. Content is accessed on a secure website in daily 10-minute sessions which transition to weekly sessions for post-operative months 3-6. In the investigators' pilot study, Veterans reported that they appreciated receiving the training in the privacy of their homes, enjoyed the interactive style of the learning experience, and felt better prepared to deal with urine leakage and empowered with new knowledge and skills to help themselves. Content for both control and treatment groups includes general information about prostate cancer; perioperative care; wetness, odor and skin care management. The treatment group will ALSO receive pelvic floor muscle training and bladder control strategies. Outcomes are measured with brief validated questions administered by the telehealth platform, and again at 9 and 12 months by mailed questionnaire or the telehealth platform.
Detailed Description
Many men develop urine leakage after radical prostatectomy. Usually it is temporary, but pelvic floor muscle training including bladder control strategies has been shown to reduce the severity of incontinence and reduce the time to regaining continence. This study will test an evidence-based pelvic floor muscle training program that has been adapted to telehealth format and pilot tested in a VA-funded pilot/developmental trial. Training is begun 1-4 weeks before surgery and continued 6 months after surgery. Content is accessed on a secure website in daily 10-minute sessions which transition to weekly sessions for post-operative months 3-6. In the investigators' pilot study, Veterans reported that they appreciated receiving the training in the privacy of their homes, enjoyed the interactive style of the learning experience, and felt better prepared to deal with urine leakage and empowered with new knowledge and skills to help themselves. This study is a randomized, controlled trial of the telehealth-delivered, evidence-based, intervention developed in the pilot/developmental study. Participants will be randomized 1:1 to treatment or to a control group. Content for both control and treatment groups includes general information about prostate cancer; perioperative care; wetness, odor and skin care management. The treatment group will ALSO receive pelvic floor muscle training and bladder control strategies. Outcomes are measured with brief validated questions administered by the telehealth platform, and again at 9 and 12 months by mailed questionnaire or the telehealth platform.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Incontinence, Prostate Cancer
Keywords
radical prostatectomy, urinary incontinence, prostate cancer, telehealth, pelvic floor muscle training

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care Provider
Allocation
Randomized
Enrollment
245 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Telehealth with Pelvic Floor Muscle Training
Arm Type
Experimental
Arm Description
Participants in this group will participate in an evidence-based pelvic floor muscle training program that has been adapted to telehealth format. Training is begun 1 month before surgery and continued 2 months after surgery. Content is accessed in 10-minute sessions on a secure website - daily preoperatively and for the first 2 months post-operatively, then weekly until 6 months post-operatively. In addition to the pelvic floor muscle training, content will also include general perioperative care; wetness, odor and skin care management; and outcome measures.
Arm Title
Telehealth without Pelvic Floor Muscle Training
Arm Type
Active Comparator
Arm Description
Participants in this group will receive a telehealth program that includes include general perioperative care; wetness, odor and skin care management; and outcome measures. The program is begun 3 weeks before surgery and continued 2 months after surgery. Content is accessed in 10-minute sessions on a secure website - daily preoperatively and for the first 2 months post-operatively, then weekly until 6 months post-operatively.
Intervention Type
Behavioral
Intervention Name(s)
Pelvic Floor Muscle Training
Intervention Description
Evidence-based pelvic floor muscle training program that has been adapted to telehealth format. Training is begun 2-4 weeks before surgery and continued 2 months after surgery. Content is accessed in daily 10-minute sessions on a secure website
Intervention Type
Behavioral
Intervention Name(s)
Perioperative Care and Wetness Management
Intervention Description
Telehealth program that includes include general perioperative care; wetness, odor and skin care management; and outcome measures. The program is begun 1-4 weeks before surgery and continued 2 months after surgery. Content is accessed in 10-minute sessions on a secure website - daily preoperatively and for the first 2 months post-operatively, then weekly until 6 months post-operatively.
Primary Outcome Measure Information:
Title
Time to Continence
Description
Time to continence was based on the time point at which participants reported no urinary incontinence on the International Consultation on Incontinence (ICI) Questionnaire-Urinary Incontinence Short Form (ICIQ-UI SF). ICIQ-UI SF is one of a series of ICI questionnaires that have been meticulously developed and tested. The ICIQ-UI SF is a brief (4 items), reliable (Cronbach's alpha = 0.95), questionnaire that quantifies both symptom burden and impact of incontinence and has been validated in men and women. It was administered weekly during the 6 months after surgery. Scores range from 0-21; higher scores indicate worse condition.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form (ICIQ-UI SF) Total Score
Description
International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form total score. Scores range from 0-21; higher scores indicate worse condition.
Time Frame
6 months, 9 months, 12 months
Title
Expanded Prostate Cancer Index Urinary Incontinence Subscale (EPIC-UI)
Description
This measure, validated as a stand-alone assessment, consists of 4 questions from the full Expanded Prostate Cancer Index (EPIC), a health-related quality of life assessment tool. The EPIC was developed based on advice from an expert panel and prostate cancer survivors, expanding the 20-item University of California - Los Angeles Prostate Cancer Index. Scores range from 0-100; higher scores indicate worse condition.
Time Frame
6 months, 9 months, 12 months
Title
Incontinence Impact Questionnaire - Short Form (IIQ-SF)
Description
This measure, validated in men with post-prostatectomy incontinence, measures the impact of incontinence on regular activities. It is a condition-specific quality of life measure that has been widely used in incontinence clinical trials. There are seven items. Response options are: "not at all," "slightly," "moderately," "greatly." Scores range from 0-100; higher scores indicate greater impact.
Time Frame
6 months, 9 months, 12 months
Title
International Prostate Symptom Scale - Quality of Life Question
Description
Validated single question: "If you were to spend the rest of your life with your urinary problem the way it is now, how would you feel about that?" Response options: delighted, pleased, mostly satisfied, mixed (about equally satisfied and dissatisfied), mostly dissatisfied, unhappy, terrible.
Time Frame
6 months, 9 months, 12 months
Title
Patient Satisfaction Question (PSQ)
Description
Patient's rating of satisfaction (Completely satisfied, Somewhat satisfied, Not at all satisfied)
Time Frame
6 months, 9 months, 12 months
Title
Estimated Percent Improvement (EPI)
Description
Participant self-report of perceived percent improvement from 0% to 100%
Time Frame
6 months, 9 months, 12 months
Title
Global Perception of Improvement (GPI)
Description
Participant's global perception of their improvement (Much better, Better, About the same, Worse, Much worse)
Time Frame
6 months, 9 months, 12 months
Title
How Disturbing is Urine Leakage
Description
Single quality of life question: "How disturbing is the urine leakage problem to you?" (not at all, somewhat, or extremely disturbing)
Time Frame
6 months, 9 months, 12 months
Title
Activity Restriction
Description
Single quality of life question: "How much does leakage of urine restrict your activities?" (not at all, some of the time, most of the time, all of the time).
Time Frame
6 months, 9 months, 12 months
Title
Return to Work
Description
Single quality of life question: "Have you been able to return to work since your surgery?" (yes, no, retired or disabled)
Time Frame
6 months, 9 months, 12 months
Title
Resumption of Normal Activity
Description
Single quality of life question: "Have you been able to resume your usual activities since your surgery?" (yes, no)
Time Frame
6 months, 9 months, 12 months

10. Eligibility

Sex
Male
Gender Based
Yes
Gender Eligibility Description
Men planning surgery for prostate cancer
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Scheduled to undergo a radical prostatectomy for treatment of prostate cancer and enrolled at the Birmingham, Philadelphia, or Atlanta VA Medical Centers or the affiliated University Medical Centers Ability to read English. Internet access Exclusion Criteria: Urinary Incontinence in the 6 months prior to prostate cancer surgery (other than post-void dribbling) Less than 1 week before surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kathryn L Burgio, PhD MA BA
Organizational Affiliation
Birmingham VA Medical Center, Birmingham, AL
Official's Role
Principal Investigator
Facility Information:
Facility Name
Birmingham VA Medical Center
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35233
Country
United States
Facility Name
Atlanta VA Medical and Rehab Center, Decatur, GA
City
Decatur
State/Province
Georgia
ZIP/Postal Code
30033
Country
United States
Facility Name
Philadelphia VA Medical Center, Philadelphia, PA
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Perioperative Post-Prostatectomy Incontinence Home Telehealth Program

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