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Differential Rehabilitative Treatment for Pelvic Floor in Sportswoman (DiRehFloor)

A

Alessandro Micarelli

Status

Invitation-only

Conditions

Pelvic Floor Disorder

Treatments

Procedure: De Gasquet arm
Procedure: Kegel arm

Study type

Interventional

Funder types

Other

Identifiers

NCT06914791
PelvicRehab1

Details and patient eligibility

About

In this study at least 24 sportswoman (18-50 years old) will be recruited a randomized in two groups which will be differently treated for the following 8 weeks. one group will be treated with Kegel approach and the other one with De Gasquet apporach. before and after the treatment they will fill in a battery of falidated questionnaire in order to evaluate the improvement at pelvic floor level, quality of life and psychological distress.

Full description

In this study at least 24 sportswoman (18-50 years old) with pelvic floow symptos (18-50 years old) will be recruited a randomized in two groups which will be differently treated for the following 8 weeks. They should havo no children, other relevant systemic disorders and assume no drugs. They should practice sports by at least one year.

one group will be treated with Kegel approach and the other one with De Gasquet apporach. before and after the treatment they will fill in a battery of falidated questionnaire in order to evaluate the improvement at pelvic floor level, quality of life and psychological distress. In partiqular they fill in:

  • Pelvic Floor Distress Inventory (PFDI-20)
  • Incontinence Severity Index (ISI)
  • Quality of life questionnaire (SF-36)
  • King's Health Questionnaire (KHQ)
  • Intestinal related symptoms questionnaire (ICIQ-B)
  • Depression Anxiety Stress Scale (DASS-21)

Enrollment

24 estimated patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • practicing sports by at least one year

Exclusion criteria

  • no systemic disorders
  • no drugs assumption
  • no children

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

24 participants in 2 patient groups

kegel arm
Active Comparator group
Treatment:
Procedure: Kegel arm
De Gasquet arm
Experimental group
Treatment:
Procedure: De Gasquet arm

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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