Completed

Effects of Physical Therapy on Pelvic Floor Symptoms and Quality of Life in Postpartum Women Following Severe Perineal Trauma: a Randomized Controlled Trial

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What is being tested

Physical Therapy (PT) and Behavioral Therapy (BT)

Behavioral
Who is being recruted

Behavior+5

+ Mental Disorders

+ Behavioral Symptoms

Over 18 Years
+10 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Prevention Study

Interventional
Study Start: September 2012
See protocol details

Summary

Principal SponsorTriHealth Inc.
Last updated: January 17, 2019
Sourced from a government-validated database.Claim as a partner

Study start date: September 12, 2012

Actual date on which the first participant was enrolled.

This is a prospective trial involving 65 woman who sustained a severe laceration or episiotomy during their first vaginal delivery to determine if postpartum intervention with physical/behavioral therapy improves their quality of life in regard to anal incontinence. The primary outcome measure is functional and based on a change in score of the Fecal Incontinence Quality of Life (FIQOL) validated questionnaire from baseline (2-weeks after delivery date) to study completion (12-weeks after delivery date). The secondary outcome measure is physiologic and reflects a change in anal sphincter resting tone from baseline to study completion. After the screening questionnaires to determine eligibility in the study, each study subject will be consented for participation then undergo a baseline physical exam (including pelvic exam and rectal exam) at a range of 2- to 4- weeks after delivery date. In addition, after this initial exam, all women will be randomized immediately to receive (1) no further treatments, or (2) physical and behavioral therapy. The investigators will study these two groups of women for 24 total weeks after the date of delivery. The intervention group will include patients randomized to receiving PT/BT for 4 weekly sessions after their vaginal delivery and laceration (episiotomy) repair. The control group (no intervention) will include patients randomized to receiving the standard of care (no physical or behavioral therapy) after their vaginal delivery and laceration (episiotomy) repair. Each group will undergo the baseline testing: a pelvic exam (to measure the strength of your muscles) and anal-rectal manometry (i.e. rectal exam with insertion of a small sensor to measure the strength of your sphincter); and be asked to complete a series of brief questionnaires. These questionnaires will be administered again to both groups at 6-weeks, 12-weeks, and 24-weeks after their delivery date. Study completion physical exams including a repeat pelvic exam and repeat anal-rectal manometry will be conducted at 12-weeks after delivery date.

Principal SponsorTriHealth Inc.
Last updated: January 17, 2019
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

54 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Prevention Study

Prevention studies aim to stop a disease from developing. They often involve people at risk and test things like vaccines, lifestyle changes, or preventive medications.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Female

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

BehaviorMental DisordersBehavioral SymptomsSigns and SymptomsSigns and Symptoms, DigestivePathological Conditions, Signs and SymptomsElimination DisordersEncopresis

Criteria

5 inclusion criteria required to participate
27 completed weeks

Able to read and speak the English language

Primiparous women aged 18 years of older

Singleton or vaginal delivery of multiple gestation

Show More Criteria

5 exclusion criteria prevent from participating
Cesarean delivery

History of prior surgery for anorectal incontinence (i.e. sphincteroplasty

Preexisting neurologic, musculoskeletal or neuromuscular disorder rendering them unable to perform physical therapy requirements

Unable to comply with physical therapy or office visits

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Intervention Group: Randomized to Physical Therapy (PT) 2-week visit which includes: Demographic Data, Physical Exam, ehavioral Therapy (BT) handouts Functional questionnaires administered Physiologic measurements obtained Follow-up Evaluation-6-week visit PT session #1 Functional questionnaires administered Follow-up Evaluation-8-week visit PT session #2 Follow-up Evaluation-10-week visit PT session #3 Study Completion Visit-12-week visit Functional questionnaires administered PT session #4 Physiologic measurements Physical Exam Long-term Follow-up-24-weeks Functional questionnaires administered by mail

Group II

No Intervention
Control Group: Baseline Data obtained at 2-week visit Demographic Data General Physical Exam findings Functional questionnaires administered in person (FIQOL, FISI, SF-12, FSFI, UDI-6, IIQ-7) Physiologic measurements obtained (Vaginal EMG, Anal-rectal manometry) Follow-up Evaluation at 6-week visit Functional questionnaires administered in person at patient's previously scheduled postpartum office visit with primary Ob/Gyn or by mail Study Completion Visit at 12-week visit Functional questionnaires administered Physiologic measurements obtained Physical Exam findings Long-term Follow-up at 24-weeks - Functional questionnaires administered by mail

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

TriHealth

Cincinnati, United StatesOpen TriHealth in Google Maps
CompletedOne Study Center