Postpartum Pelvic Floor Rehabilitation and Information Provided by the Health Care Providers

• Conditions: Recovery of Function

• Registration Number: NCT04882722
• Lead Sponsor: Centre Hospitalier Departemental Vendee

Brief Summary

The aim of this work is to evaluate the experience of Postpartum Pelvic Floor Rehabilitation (PPFR) according to the information given by the health care providers. There is to improve medical practice and to give the right information in at the right time to the patient.

Detailed Description

Postpartum Pelvic Floor Rehabilitation is an important central stage of the postpartum period. It allows, if it is well done, to reduce complications related to childbirth, (pelvic floor disorders: urinary, sexual or anal disorders ) and to increase quality of life of women in postpartum period.

But, what about the woman's opinion and experience of PPFR? Previous studies have evaluated the effectiveness of PPFR but not the woman's experience.

It is interesting to evaluate the experience of PPFR according to the information given by the health care providers. There is to improve medical practice and to give the right information in at the right time to the women

Study Timeline

• Status Verified: 2021-04
• Study First Submitted: 2021-04-28
• Study First Submitted QC: 2021-05-06
• Study First Posted: 2021-05-12
• Study Start: 2021-05-25
• Last Update Submitted: 2021-07-29
• Last Update Posted: 2021-07-30
• Primary Completion: 2021-12-31
• Study Completion: 2022-02-01

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: Female
• Target Recruitment: 50

Inclusion Criteria

• All women undergoing postpartum pelvic floor rehabilitation at the Departmental Hospital Center of Vendee

Exclusion Criteria

• Refusal to participate in the study
• Patient did not complete all her PPFR sessions at the Departmental Hospital Center of Vendee
• Patient unable to understand the protocol, read the information note and answer the questionnaires
• Patient under tutelage, curatorship, mandate of future protection, family habilitation

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Overall experience of the PPFR according to information given by the health care providers	through study completion, an average of 5 weeks	Self-evaluation of the overall experience of postpartum pelvic floor rehabilitation

Trial Locations

Locations (1)

Departmental Hospital Center of Vendee; 🇫🇷 La Roche sur Yon, France