Pelvic Floor Muscle Weakness
Conditions
Keywords
Smartphone Applications, Home exercise program, Adherence
Brief summary
The goal of this randomized clinical trial is to investigate the impact of a smartphone-based application on patient-reported outcomes for patients with pelvic floor muscle weakness, and the relationship of patient adherence to outcomes in pelvic floor physical therapy compared to the paper-based standard of care. An additional aim is the exploration and development of two patient-reported questionnaires to enhance understanding of exercise adherence in outpatient pelvic floor physical therapy and smartphone application self-efficacy. These goals will serve to improve practice recommendations for home exercise prescriptions in this patient population. Participants will be asked to complete 6 patient-reported outcome measures after they complete four, 60-minute long physical therapy treatment sessions conducted one time per week according to the current standard of care for pelvic floor physical therapy. The experimental group will be given a free pelvic floor muscle exercise application while the control group will be provided with the paper-based standard of care for their home exercise program.
Interventions
BEHAVIORALA smartphone based application free to download from the google play and iphone store to provide auditory and visual cues and counting for number of perscribed pelvic floor muscle contractions
Use of a smartphone-based home exercise application for pelvic floor muscle exercises with visual and auditory feedback for 10 repetitions of pelvic floor contraction endurance holds and 10 repetitions of pelvic floor quick contractions performed three times per day.
BEHAVIORALPaper-based home exercise program for pelvic floor muscle exercise
Written instructions on a piece of paper for 10 repetitions of pelvic floor contraction endurance holds and 10 repetitions of pelvic floor quick contractions performed three times per day.
Sponsors
University of Central Arkansas
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Masking description
Participants were blinded to their group allocation and were not aware that another treatment existed until debriefing and unblinding.
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 85 Years
Healthy volunteers
No
Inclusion criteria
* 18-85 years old * Referred to outpatient pelvic floor physical therapy for treatment of pelvic floor weakness * Generation 5 or later iPhone, Android, or Smart Device * Must be willing to receive Push Notification reminders from the application * Must have free space on device to download and install app * Must have access to the Google Play store or to iOS Apple App Store
Exclusion criteria
* ● Not Meeting Inclusion Criteria * Pelvic Organ Prolapse Surgery with complications * Neurodegenerative Disease * History of TBI or CVA with resulting impairment in long- or short-term memory * Denervation injury to the pelvic floor * Spinal cord injury * Pelvic Pain Condition * Incapable of Completing Outcomes Questionnaire without caregiver support * Unable to speak and read English * Current Pregnancy * Less than 6 weeks postpartum * Researcher judgement
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pelvic Floor Distress Inventory short-form 20 (PFDI-20) | From date of randomization through study completion, an average of 3 months. | Patient-reported health-related quality of life outcome measures that are widely used for assessment of pelvic floor dysfunction. The minimum score is 0, and the maximum score is 300. HIgher scores indicate higher levels of dysfunction and mean a worse outcome, lower levels indicate less dysfunction and a better outcome. |
Countries
United States
Outcome results
None listed