Physiotherapy Management in Women With Urinary Incontinence

Sponsor
Poznan University of Physical Education
Study ID
NCT06581601
Status
Recruiting
Apply to this trial

Conditions

  • Urinary Incontinence

Eligibility Criteria

Sex
FEMALE
Age
20 Years - 80 Years
Healthy Volunteers
Accepted

Interventions

  • physiotherapy, exercises — OTHER
    An author's questionnaire will be used for participant selection, asking about the number and course of deliveries. Additionally, participants will log daily activities to calculate the physical activity level coefficient. Weight and height will be measured using a Tanita device to calculate BMI. The posture type and pelvic type will be assessed. Participants will be asked to complete the following questionnaires before and after the intervention: Pelvic Floor Disability Index (PFDI-20), Pelvic Floor Impact Questionnaire Short Form (PFIQ-7 SF), Sexual Satisfaction Scale (SSS-W-R15), Neck Disability Pain Index, Revised Oswestry Low Back Pain Disability Scale, Migraine Disability Assessment (MIDAS), Hospital Anxiety and Depression Scale (HADS), Short Form McGill Pain Questionnaire, CRANIA (Integrated Approach to Cranio Mandibular Neuroscience) questionnaire, IPAQ (International Physical Activity Questionnaire). Modified 1-Hour Pad Test. Execution of the Author's Training Program.

Study Details

Main objective: The primary aim of the study is to assess whether the author's exercise programme has an effect on reducing urinary incontinence and pelvic floor dysfunction after childbirth, considering vacuum extractor, forceps and caesarean section deliveries. Secondary objective: The secondary objective is to determine whether the duration of the author's exercise programme is sufficient to achieve positive changes in women.

Key Dates

First listed
Sep 3, 2024
Start date
Aug 21, 2024
Status verified
Nov 2024
Primary completion
Nov 20, 2027
Completion
Nov 20, 2027

Study Design

Enrollment
300 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION

Arms

  • No Intervention: Control group
    1.Contorl group: healtyhy women.
  • Experimental: Pre-menopausal group
    2.Pre-menopasal group: experimental group - exercise's group
  • Experimental: Post-menopausal group
    3.Post-menopausal group: experimental group - exercise's group

Primary Outcome Measure

Modified 1-Hour Pad Test, measurement in grams [ Time Frame: before start exercises and after six week finish exercises ]

Central Contacts

Related Studies