Effect of Text Message Reminders on M-ISI Score After Prostate Surgery

Clinicaltrials.gov ID: NCT07071207
db-list-check Status RECRUITING
b-loader Phase NA
b-people Age ≥ 18 Years
b-bullseye-arrow Enrollments 132

Conditions

Incontinence, Urinary Stress, Prostate Cancer, Benign Prostate Hyperplasia

Summary

The purpose of this study is to compare post-prostatectomy incontinence via Michigan Incontinence Score Index in patients receiving daily text message reminders for pelvic floor exercises when compared to those not receiving text reminders.

Detailed Description

This trial will be comprised of prostate cancer patients who have undergone a radical prostatectomy and benign prostate hyperplasia patients who have undergone a laser enucleation of the prostate. These two cohorts will each be split into an intervention and a control group. The purpose of this study is to evaluate post-prostatectomy incontinence via patient reported outcomes utilizing Michigan Incontinence Score Index in patients receiving daily text message reminders for pelvic floor exercises + standard of care (intervention group) compared to those receiving standard of care only (control group).

Locations

1 location Found with status Recruiting

Status

  • RECRUITING

Central Contacts

Eligibility Criteria

Inclusion Criteria:

1. Planning to undergo a radical prostatectomy (RALP) or laser enucleation of the prostate (LEP) procedure
2. Patient of URMC Urology
3. Adult male 18 years of age and older
4. Able to read, write, and speak in English (NOTE: due to limitations with questionnaire validation, only English-speaking subjects are permitted)
5. Has access to a mobile device capable of receiving automated text messages.
6. Willing to receive text messages and to complete questionnaires via SMS text.
7. Willingness to participate and able to provide informed consent.

Exclusion Criteria:

1. Less than 18 years of age
2. Unable to send and receive SMS texts
3. Unable to read, write, and speak English
4. Catheter dependency
5. Has or plans to have Artificial Urinary Sphincter or Urethral Sling during the study period
6. In the opinion of the investigator, the subject has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the study, interfere with the subject's participation for the full duration of the study, or is not in the best interest of the subject to participate.

Study Plan

Control group - LEP surgery patients

NO_INTERVENTION

Patients undergoing LEP surgery and standard of care discharge instructions to perform pelvic floor exercises

    Intervention group - LEP surgery patients

    EXPERIMENTAL

    Patient undergoing LEP surgery with text message intervention to perform pelvic floor exercises as described in the schedule of events

    • BEHAVIORAL:

      Text message reminders

      Description:

      daily 8am text messages reminding patients to perform Kegel exercises as per their standard-of-care post-operative discharge instructions.

    Control group - RALP surgery patients

    NO_INTERVENTION

    Patients undergoing RALP surgery and standard of care discharge instructions to perform pelvic floor exercises

      Intervention group - RALP surgery patients

      EXPERIMENTAL

      Patient undergoing RALP surgery with text message intervention to perform pelvic floor exercises as described in the schedule of events

      • BEHAVIORAL:

        Text message reminders

        Description:

        daily 8am text messages reminding patients to perform Kegel exercises as per their standard-of-care post-operative discharge instructions.

      Outcome Measures

      Primary Outcome Measures

      Time to Recovery to Continence

      Time Frame: From baseline until the participant reaches two successive M-ISI Pad Use Subdomain Scores of u2264 2, assessed up to 12 months

      Timeline

      • Last Updated
        November 6, 2025
      • Start Date
        July 17, 2025
      • Today
        December 16, 2025
      • Completion Date ( Estimated )
        May 1, 2028

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