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

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04882722
Acronym
PPFR
Enrollment
50
Registered
2021-05-12
Start date
2021-05-25
Completion date
2022-02-01
Last updated
2021-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Recovery of Function

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

Interventions

OTHERQuestionnaire

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

Sponsors

Centre Hospitalier Departemental Vendee
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Overall experience of the PPFR according to information given by the health care providersthrough study completion, an average of 5 weeksSelf-evaluation of the overall experience of postpartum pelvic floor rehabilitation

Countries

France

Contacts

Primary ContactAgnès Dorion
agnes.dorion@chd-vendee.fr251446380

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026