Effectiveness of an 8-week Independent Cadence Retraining Program on Stress Urinary Incontinence in Parous Runners.

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorMayo Clinic

About this trial

The purpose of this research is to assess the impact of an eight-week home cadence training program on stress urinary incontinence symptoms in parous women.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Healthy

Nonpregnant

Female volunteers

Self-reported urinary incontinence during running with history of at least one prior delivery after 32 weeks gestation and who run 6 miles/week with a preferred cadence of less than or equal to 170 steps per minute determined via personal report from current Garmin watch data.

Disqualifiers

Unwillingness to complete all components of the study

Urge only urinary incontinence

<3 months postpartum or current pregnancy

History of prolapse repair or incontinence surgery

Trial design

Design model

Parallel

Treatments tested in this trial

  • Cadence Increase

    Other intervention

    Utilizing cadence alarm on a garmin device, the intervention group will attempt to increase their running cadence by 10%.

  • Cadence Maintenance

    Other intervention

    Participants will use cadence alarms to maintain preferred running cadence.

Treatment groups

66 Participants
are divided into 2 treatment groups
Group A: Cadence increase groupExperimental treatment 1 intervention
Group B: Cadence Maintenance ArmPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Preferred Cadence

Participants will self-assess preferred running cadence using a garmin device during a 15 minute self-paced run.

Time frame
Baseline and 8 weeks
2

The Pelvic Floor Distress Inventory-20 (PFDI-20)

questionnaire that assesses bowel, bladder, and pelvic symptoms and their impact on quality of life. Scores range from 0 to 300 with higher scores indicating greater pelvic floor distress and impact on quality of life.

Time frame
Baseline, 8 weeks, and 6 month
3

Questionnaire for Female Urinary Incontinence Diagnosis (QUID)

6 item urinary incontinence questionnaire. A higher SUI score (range 0-15) suggests stress urinary incontinence is more likely. A higher UUI score (range 0-15) suggests urge urinary incontinence is more likely. The questionnaire is designed to help distinguish between these two main types of urinary incontinence in women.

Time frame
Baseline, 8 weeks, and 6 months
4

International Consultation on Incontinence Questionnaire - Urinary Incontinence (ICIQ-UI)

The ICIQ-UI Short Form (ICIQ-UI SF) produces a single score from 0 to 21 by summing three scored items: leakage frequency, leakage amount, and impact on daily life. A higher score indicates increased severity of urinary incontinence symptoms.

Time frame
Baseline, 8 weeks, and 6 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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