CClinicalTrials.gg
Status unknownNCT04882722PPFRUpdated Jul 30, 2021

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

An observational study in Recovery of Function, sponsored by Centre Hospitalier Departemental Vendee. Status unknown at 1 site in France. Open to female participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2021-07-30.

Sponsored by Centre Hospitalier Departemental Vendee · Observational

The sponsor has not verified this record recently (last verified Apr 2021), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
50
Ages
18 Years to 50 Years
Sex
Female
01

Study 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.

Read the 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

02

Conditions studied

  • Recovery of Function
03

In context

Lead sponsor

Centre Hospitalier Departemental Vendee is the lead sponsor of 81 studies on the registry; 12 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

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

Inclusion criteria

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

Exclusion criteria

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
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
50 participants (estimated)
Patient registry
No

Interventions

  • OtherQuestionnaire

    Self-questionnaire reported before the first PPFR session and after the last session

06

What researchers measure

Primary outcomes

  1. 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

    Time frame: through study completion, an average of 5 weeks

07

Study locations

1 of 1 sites recruiting
  • Departmental Hospital Center of Vendee
    La Roche sur Yon, 85000, France
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 30, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04882722
Lead sponsor
Centre Hospitalier Departemental Vendee
Responsible party
Sponsor
First posted
May 12, 2021
Start date
May 25, 2021
Primary completion
Dec 31, 2021 (estimated)
Completion
Feb 1, 2022 (estimated)
Last update
Jul 30, 2021

Study contacts

Agnès Dorion
Contact
agnes.dorion@chd-vendee.fr
251446380 ext. +33
Guillaume DUCARME, Dr
principal investigator · Departmental Hospital Center of Vendee

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2021. You cannot join it, but the record below documents what was studied.

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