NCT07228806 Effectiveness of Telerehabilitation on Pelvic Floor Dysfunction at Postpartum Woman
| NCT ID | NCT07228806 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Ankara Etlik City Hospital |
| Condition | Postpartum Pelvic Floor Function and Symptoms |
| Study Type | INTERVENTIONAL |
| Enrollment | 60 participants |
| Start Date | 2025-11-30 |
| Primary Completion | 2026-05-09 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 60 participants in total. It began in 2025-11-30 with a primary completion date of 2026-05-09.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
These events are largely due to pelvic floor dysfunction that develops after pregnancy. Kegel exercises and core stabilisation exercises performed in the postpartum period are important in preventing pelvic floor dysfunction. However, considering the mother's adaptation process to both the baby and her new life in the postpartum period, there may be problems with exercise compliance. Increasing exercise compliance through telerehabilitation can be effective in preventing pelvic floor dysfunction and improving women's quality of life.
Eligibility Criteria
Inclusion Criteria: 1. Aged between 18 and 45 2. Primiparous women 3. Term vaginal delivery 4. 6 weeks postpartum 5. Willingness to participate in the study Exclusion Criteria: 1. Presence of faecal or urinary incontinence prior to pregnancy 2. Use of assisted delivery devices (vacuum, forceps) 3. Presence of neurological disease 4. Presence of psychiatric illness or cognitive problems that make it difficult to answer questions 5. Caesarean section delivery 6. History of diabetes mellitus 7. Perineal rupture
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07228806 clinical trial?
This trial is open to female participants only, aged 18 Years or older, up to 45 Years, studying Postpartum Pelvic Floor Function and Symptoms. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07228806 currently recruiting?
Yes, NCT07228806 is actively recruiting participants. Contact the research team at kalemnaz@gmail.com for enrollment information.
Where is the NCT07228806 trial being conducted?
This trial is being conducted at Ankara, Turkey (Türkiye).
Who is sponsoring the NCT07228806 clinical trial?
NCT07228806 is sponsored by Ankara Etlik City Hospital. The trial plans to enroll 60 participants.