ACTIVE_NOT_RECRUITING

Mobility and Voiding Exercises in Older Women With Urinary Incontinence (MoVEonUp)

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Conditions

Urinary Incontinence, Urge

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

A prospective, two-arm randomized clinical trial utilizing a multidimensional intervention to reduce falls in older women with Urinary Urge Incontinence. The intervention consist of general balance and strength training, bladder training and urge suppression, and home hazard assessments. The control group will receive informational booklets on fall prevention and behavioral treatment for urinary urge incontinence.

Official Title

MoVE on Up: Mobility and Voiding Exercises in Older Women With Urinary Incontinence

Quick Facts

Study Start:2022-06-09
Study Completion:2026-09
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05375344

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:70 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Female
  2. * 70 or older
  3. * Living independently in the community
  4. * Willingness to be randomized.
  5. * Ability to read and understand English
  6. * Be able to provide informed consent
  7. * Low physical activity (physically active for 30 minutes or more less than or equal to 2 days per week on average over the past 6 months) per PAS
  8. * Ambulatory (defined as patient not confined to bed or wheelchair OR ability to walk with or without an assistive device)
  9. * Self-reported moderate to severe urge-predominant UI based on the ICIQ-SF \> 6 (Q 1+2+3)
  10. * Not planning to initiate new UI or overactive bladder (OAB) treatment during the study duration
  11. * Capable of participation in an exercise program without exacerbating any pre-existing condition(s), as determined by the study PI or designee
  1. * Pelvic organ prolapse passed the hymen (per patient report)
  2. * Undergoing active treatment for cancer (other than non-melanoma skin cancer)
  3. * Uncorrected visual or hearing loss.
  4. * Other urinary conditions or procedures that may affect continence status for example: urethral diverticulum, previous augmentation cystoplasty
  5. * Progressive neurodegenerative disease e.g. Parkinson's disease, multiple sclerosis per patient report
  6. * History of stroke or carotid sensitivity (i.e. syncopal falls) per patient report
  7. * Unstable cardiac disease per patient report
  8. * Fracture or joint replacement within the last six months per patient report
  9. * Significant cognitive impairment (defined as a modified TICs score of \< 27)
  10. * Per PI discretion, participant cannot enroll in study

Contacts and Locations

Principal Investigator

Uduak U Andy, MD
PRINCIPAL_INVESTIGATOR
University of Pennsylvania

Study Locations (Sites)

University of Pennsylvania
Philadelphia, Pennsylvania, 19104
United States

Collaborators and Investigators

Sponsor: University of Pennsylvania

  • Uduak U Andy, MD, PRINCIPAL_INVESTIGATOR, University of Pennsylvania

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-06-09
Study Completion Date2026-09

Study Record Updates

Study Start Date2022-06-09
Study Completion Date2026-09

Terms related to this study

Additional Relevant MeSH Terms

  • Urinary Incontinence, Urge