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

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

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.

Study Overview

• Status: Recruiting
• Conditions: Recovery of Function
• Intervention / Treatment: Other: Questionnaire

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 Type: Observational
• Enrollment (Anticipated): 50

Contacts and Locations

• Study Contact: Name: Agnès Dorion; Phone Number: +33 251446380; Email: agnes.dorion@chd-vendee.fr

Study Locations

• France
  • La Roche sur Yon, France, 85000
    • Recruiting
    • Departmental Hospital Center of Vendee
    • Contact: Guillaume DUCARME; Email: guillaume.ducarme@chd-vendee.fr
    • Principal Investigator: Guillaume Ducarme, Dr

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 50 years (Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: Female

• Sampling Method: Non-Probability Sample

Study Population

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

Description

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 Plan

How is the study designed?

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
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

Collaborators and Investigators

• Sponsor: Centre Hospitalier Departemental Vendee
• Investigators: Principal Investigator: Guillaume DUCARME, Dr, Departmental Hospital Center of Vendee

Study record dates

Study Major Dates

• Study Start (Actual): May 25, 2021
• Primary Completion (Anticipated): December 31, 2021
• Study Completion (Anticipated): February 1, 2022

Study Registration Dates

• First Submitted: April 28, 2021
• First Submitted That Met QC Criteria: May 6, 2021
• First Posted (Actual): May 12, 2021

Study Record Updates

• Last Update Posted (Actual): July 30, 2021
• Last Update Submitted That Met QC Criteria: July 29, 2021
• Last Verified: April 1, 2021

More Information

Terms related to this study

• Other Study ID Numbers: CHD21_0027

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No