WithdrawnNot Applicable

Quality and Behavior of Pelvic Floor in Runner Women

Stopped: Stopped PhD project

Spain0Started 2021-06-01

Plain-language summary

The main objective is to analyze the relationship between the PF muscles and the other variables along the different tasks of daily life and during the race.

Who can participate

Age range25 Years – 44 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Healthy woman between 25 and 44 years old. * Women not pregnant. * Women who run at least 10 km / week. * In case of having children, it has to be 12 months after childbirth, having had the first postpartum menstruation and having left breastfeeding. Exclusion Criteria: * Women Pregnant or suspected of it. * Postpartum less than one year. * Having the period during the exploration for the classification in groups or during the day of the measurements. * Present operation in the urogenital region as well as any visceral or spinal operation. * Urinary tract and/or vaginal infections. * Vaginal lesions; anorectal lesions or bleeding. * Women with gynecological bleeding; urethral obstruction; fistulas; malformations (ectopic ureter, etc); genital prolapse. * Women with pain in Pelvic Floor or lower limbs or back. * Pain during the race. * Allergy to silver, nickel and/or latex.

What they're measuring

Change %MVC

Timeframe: Prior and after intervention, an average of 12 weeks

Change of Base Tone of Pelvic Floor Muscles (EMG)

Timeframe: baseline, prior and after intervention, an average of 12 weeks

Change of step length

Timeframe: Prior and after intervention, an average of 12 weeks

Change of cadence

Timeframe: Prior and after intervention, an average of 12 weeks

Change of ground reaction force

Timeframe: Prior and after intervention, an average of 12 weeks

Change of acceleration

Timeframe: Prior and after intervention, an average of 12 weeks

Change of displacement

Timeframe: Prior and after intervention, an average of 12 weeks

Change of accumulated fatigue

Timeframe: Prior and after intervention, an average of 12 weeks

Trial details

NCT IDNCT03934996

SponsorUniversity of Malaga

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-07-01

View on ClinicalTrials.gov More Pelvic Floor Disorders trials

Who can participate

Age range25 Years – 44 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Change %MVC

Timeframe: Prior and after intervention, an average of 12 weeks

Change of Base Tone of Pelvic Floor Muscles (EMG)

Timeframe: baseline, prior and after intervention, an average of 12 weeks

Change of step length

Timeframe: Prior and after intervention, an average of 12 weeks

Change of cadence

Timeframe: Prior and after intervention, an average of 12 weeks

Change of ground reaction force

Timeframe: Prior and after intervention, an average of 12 weeks

Change of acceleration

Timeframe: Prior and after intervention, an average of 12 weeks

Change of displacement

Timeframe: Prior and after intervention, an average of 12 weeks

Change of accumulated fatigue

Timeframe: Prior and after intervention, an average of 12 weeks