Perioperative Post-Prostatectomy Incontinence Home Telehealth Program
NCT ID: NCT01960998
Last Updated: 2021-08-09
Study Results
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View full resultsBasic Information
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COMPLETED
NA
245 participants
INTERVENTIONAL
2014-08-11
2019-09-30
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Telehealth with Pelvic Floor Muscle Training
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.
Pelvic Floor Muscle Training
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
Perioperative Care and Wetness Management
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.
Telehealth without Pelvic Floor Muscle Training
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.
Perioperative Care and Wetness Management
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.
Interventions
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Pelvic Floor Muscle Training
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
Perioperative Care and Wetness Management
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.
Eligibility Criteria
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Inclusion Criteria
* Ability to read English.
* Internet access
Exclusion Criteria
* Less than 1 week before surgery
MALE
Yes
Sponsors
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Emory University
OTHER
University of Pennsylvania
OTHER
University of Alabama at Birmingham
OTHER
VA Office of Research and Development
FED
Responsible Party
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Principal Investigators
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Kathryn L Burgio, PhD MA BA
Role: PRINCIPAL_INVESTIGATOR
Birmingham VA Medical Center, Birmingham, AL
Locations
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Birmingham VA Medical Center
Birmingham, Alabama, United States
Atlanta VA Medical and Rehab Center, Decatur, GA
Decatur, Georgia, United States
Philadelphia VA Medical Center, Philadelphia, PA
Philadelphia, Pennsylvania, United States
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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D1059-R
Identifier Type: -
Identifier Source: org_study_id
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