Clinical Trials Directory

Trials / Completed

CompletedNCT03287258

Perineal Preparation for Pregnant Ladies.

Digital Perineal Massage and Pelvic Floor Muscle Exercise as an Antenatal Program for Prevention of Perineal Trauma in Elderly Women, a Randomized Controlled Trial.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
400 (actual)
Sponsor
Kasr El Aini Hospital · Academic / Other
Sex
Female
Age
35 Years – 45 Years
Healthy volunteers
Accepted

Summary

Pregnant participants will be recruited at the obstetrics outpatient clinic during their visits 4 weeks before the due date. They are randomized into two groups. The first group will be educated to do digital perineal massage. They will be also educated to do pelvic floor muscle exercises and will receive the usual education program for strengthening the pelvic floor. The second group will receive the usual education program for strengthening the pelvic floor. Occurrence of perineal laceration will be reported at time of delivery.

Detailed description

Pregnant participants will be recruited at the obstetrics outpatient clinic during their visits 4 weeks before the due date. They are randomized into two groups. The first group will be educated to do digital perineal massage. They will be also educated to do pelvic floor muscle exercises and will receive the usual educational pelvic floor dysfunction prevention program for strengthening the pelvic floor. The second group will receive the usual education program for strengthening the pelvic floor. Occurrence of perineal laceration will be reported at time of delivery.

Conditions

Interventions

TypeNameDescription
OTHER3 programThe participants will receive 3 programs.The educational pelvic floor dysfunction prevention program, pelvic floor muscle exercise program and perineal massage program will be educated by an investigator during the participant visit 4 weeks before her due date
OTHERone programThe participants will receive one program. That is the educational pelvic floor dysfunction prevention program.The instructions of the program will be given by an investigator once during the participant visit 4 weeks before her due date.

Timeline

Start date
2017-04-25
Primary completion
2017-07-20
Completion
2017-12-31
First posted
2017-09-19
Last updated
2018-11-02

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03287258. Inclusion in this directory is not an endorsement.