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Prevention of Female Pelvic Floor Dysfunction Rehabilitation Postpartum.

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The main goal of this study to compare self-training postpartum and training with a specialist support (physiotherapist and physical medicine and rehabilitation doctor) effect on pelvic floor dysfunction prevention and treatment in postpartum period. Hypothesis: The implementation of postpartum rehabilitation helps to alleviate existing symptoms of pelvic floor dysfunction and prevents pelvic floor dysfunction. Study goals: * To objectively evaluate changes in pelvic organ position and pelvic floor muscle function in postpartum period, before and after specialised rehabilitation program * To objectively evaluate pelvic floor symptoms and their influence on woman life quality * To compare data (changes in pelvic floor muscle coordination and strength, pelvic organ position and changes in life quality according to validated questionnaires) Study participants will: * Get an examination by obstetrician-gynaecologist, physical medicine and rehabilitation doctor and physiotherapist in 6 to 10 weeks postpartum period. * One group of participants will attend physiotherapy, biofeedback and electro stimulation procedures with a guidance of a specialist. * Other group of participants gets a recommendations and instructions of training and self-trains at home. To remind of training and help record training time squeezy app (an application designed for a mobile device) will be offered. * All groups of participants will be asked to fill life quality related questionnaires: (ICIQ-UI SF: International Consultation on Incontinence Questionnaire; P-QoL: Prolapse Quality-of-Life Questionnaire; PISQ-IR: Pelvic Organ Prolapse/ Urinary Incontinence Sexual Questionnaire IUGA revised; FSFI: female sexual function index; MOS-SF36 Medical Outcomes Study Short Form-36).

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 50
Healthy Volunteers: t
View:

• 18 years or older

• This pregnancy was singleton

• No contraindications for physical activity

• No connective tissue disorders (for example Ehlers-Danlos syndrome)

• No neurological disorders to influence pelvic floor symptoms (for example clinically significant spinal disc herniation)

Locations
Other Locations
Lithuania
Vilnius University: study centers: Vilnius University Hospital Santaros Clinic, Vilniaus Gimdymo Namai
RECRUITING
Vilnius
Contact Information
Primary
Karolina Eva Romeikiene, Medical doctor, PHD student
eva.romeikiene@gmail.com
+37060406142
Time Frame
Start Date: 2024-01-30
Estimated Completion Date: 2029-09-30
Participants
Target number of participants: 80
Treatments
Active_comparator: Group of participants getting specialist supervised training postpartum
Woman 6-10 weeks postpartum starts training program with physiotherapist and physical medicine and rehabilitation physician supervision.
Other: Group of participants doing self-training with an app
Woman 6-10 weeks postpartum starts self- training program at home. At the beginning they are instructed by physiotherapist and physical medicine and rehabilitation physician. This group use an app squeezy to remind the to do training and record training time.
Sponsors
Collaborators: Vilnius University Hospital Santaros Klinikos, Vilnius Maternity Hospital
Leads: Vilnius University

This content was sourced from clinicaltrials.gov