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

Sponsor
Centre Hospitalier Departemental Vendee (Other)
Overall Status
Recruiting
CT.gov ID
NCT04882722
Collaborator
(none)
50
Enrollment
1
Location
8.3
Anticipated Duration (Months)
6
Patients Per Site Per Month

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • 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 Design

Study Type:
Observational
Anticipated Enrollment :
50 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Opinion Survey on Postpartum Pelvic Floor Rehabilitation According to the Quality of Information Provided by the Health Care Providers
Actual Study Start Date :
May 25, 2021
Anticipated Primary Completion Date :
Dec 31, 2021
Anticipated Study Completion Date :
Feb 1, 2022

Outcome Measures

Primary Outcome Measures

  1. 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

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 50 Years
Sexes Eligible for Study:
Female
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Departmental Hospital Center of Vendee La Roche sur Yon France 85000

Sponsors and Collaborators

  • Centre Hospitalier Departemental Vendee

Investigators

  • Principal Investigator: Guillaume DUCARME, Dr, Departmental Hospital Center of Vendee

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Departemental Vendee
ClinicalTrials.gov Identifier:
NCT04882722
Other Study ID Numbers:
  • CHD21_0027
First Posted:
May 12, 2021
Last Update Posted:
Jul 30, 2021
Last Verified:
Apr 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jul 30, 2021