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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02846480
Other study ID # UAlcala_POP
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 2010
Est. completion date June 2017

Study information

Verified date February 2016
Source University of Alcala
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To find out the effectiveness of physical therapy associated with the surgical treatment over the simptoms and quality of life in III and IV grades of pelvic organ prolapse, patients will be randomly assigned to one of these groups: experimental group: pre-surgical and post-surgical physical therapy + behavioral education + surgical therapy. Control group: surgical treatment + behavioral education.

In both groups several physical therapy assessments will be undertaken: 1st before surgery; 2nd immediately after surgery; and after 6 weeks, 3th, 6th, 12th and 24th months post-surgery.


Description:

Intervention in the experimental group, patients assigned to this group will receive:

- Pre-surgical physical therapy: 9 sessions of physical therapy aimed at correcting posture, to the awareness and the strengthening of the pelvic floor muscles. They will be also informed and instructed on hygienic and behavioral education to prevent pelvic organ prolapse and urinary incontinence. Each session will be about 45 minutes and 3 sessions will be held a week for 3 weeks.

- Post-surgical Physical Therapy:

2. Hospital discharge patients will receive the same fact sheet on sanitary and behavioral measures recommended for the prevention of pelvic organ prolapse and urinary incontinence.

3. 6th weeks after surgery: 8 physical therapy sessions (2 per week for 4 weeks) about 30 minutes to review hypopressive exercises and contractions of the pelvic floor.

Intervention in the control group, patients assigned to this group will receive:

After surgical correction of pelvic organ prolapse, at hospital discharge, patients will receive a fact sheet on the sanitary and behavioral measures recommended for the prevention of pelvic organ prolapse and urinary incontinence (proper weight, prevent constipation, avoid weight bearing and cough and high impact exercise). No physical therapy intervention will be performed.


Recruitment information / eligibility

Status Completed
Enrollment 65
Est. completion date June 2017
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Consecutive women diagnosed with grade III and IV pelvic organ prolapse, which would be operated for this reason at the Asturias Prince Hospital (Madrid-Spain).

Exclusion Criteria:

- Women diagnosed with different III / IV grade of POP or a history of conservative treatment not from the subproject "Physiotherapy in the POP grades I and II", or a history of POP surgery, or concurrent conditions that would be affect the treatment (neurological, gynecological or urological), or recurrent urinary infection or hematuria, or those III / IV grades in POP which is contraindicated or not possible to perform surgery.

- Pregnant women or women with a vaginal birth in the last six months.

- Women with cognitive limitations to understand the information, answer questionnaires, consent and / or participate in the study.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
physical therapy
Pre-surgical Physical Therapy: physical therapy aimed to correct the posture, to the awareness and the strengthening of the pelvic floor muscles. Post-surgical Physical Therapy: checking the correct contraction of the pelvic floor muscles and hypopressive exercises.
surgical treatment
Surgical correction of POP.
behavior therapy
At hospital discharge, patients will receive a fact sheet on the sanitary and behavioral measures recommended for the prevention of POP and urinary incontinence (proper weight, prevent constipation, avoid weight bearing and cough and high impact exercise).

Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
BEATRIZ SANCHEZ SANCHEZ Hospital Universitario Principe de Asturias, Instituto de Salud Carlos III

Outcome

Type Measure Description Time frame Safety issue
Primary The SF-12 Health Survey (SF-12) Spanish version up to 24th months post-surgery.
Primary Assessment of pelvic floor muscles strength with Modified Oxford Scale and vaginal perineometry, vaginal dynamometry up to 24th months post-surgery.
Primary International Consultation on Incontinences Short Form (ICIQ-SF) Spanish version. up to 24th months post-surgery.
Secondary Urinary symptoms (urinary frequency, nocturia, urgency, incontinence, coital incontinence, nocturnal enuresis, frequency of urinary tract infections, dysuria and urinary difficulty). up to 24th months post-surgery.
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