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

Recovery of Function Clinical Trial

— PPFR  

Official title:

Opinion Survey on Postpartum Pelvic Floor Rehabilitation According to the Quality of Information Provided by the Health Care Providers

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04882722
• Other study ID #: CHD21_0027
• Status: Recruiting
• Start date: May 25, 2021
• Est. completion date: February 1, 2022

Study information

• Verified date: April 2021
• Source: Centre Hospitalier Departemental Vendee
• Contact: Agnès Dorion
• Phone: 251446380
• Email: agnes.dorion[@]chd-vendee.fr
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

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

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 50
• Est. completion date: February 1, 2022
• Est. primary completion date: December 31, 2021
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 50 Years

Eligibility

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

Related Conditions & MeSH terms

• Recovery of Function

Intervention

Other:
• Questionnaire
Self-questionnaire reported before the first PPFR session and after the last session

Locations

Country	Name	City	State
France	Departmental Hospital Center of Vendee	La Roche sur Yon

Sponsors (1)

Lead Sponsor	Collaborator
Centre Hospitalier Departemental Vendee

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall experience of the PPFR according to information given by the health care providers	Self-evaluation of the overall experience of postpartum pelvic floor rehabilitation	through study completion, an average of 5 weeks