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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05682157
Other study ID # RCT-PAULA-LARS-HMO-CTIL
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 21, 2023
Est. completion date October 1, 2025

Study information

Verified date February 2024
Source Hadassah Medical Organization
Contact Noam Shussman, MD
Phone +972 2 6779758
Email noams@hadassah.org.il
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Sphincter sparing rectal resection surgery, either total mesorectal excision (TME) with a temporary loop ileostomy or partial mesorectal excision (PME), is the mainstay of rectal cancer treatment , however, these treatments are associated with the development of Low anterior resection syndrome (LARS). This syndrome is characterized by a constellation of symptoms such as fecal frequency, urgency and clustering of bowel movements and can lead to fecal and flatus incontinence. There is no gold standard therapy designed to treat the root cause of the problems associated with LARS. Paula Method of exercises, based on the theory that the body has the natural ability to self-heal and that all sphincter muscles in the body affect one another other and thus, exercising one healthy region can positively impact another. The purpose of this study is to evaluate the usefulness of the Paula Method of exercises in patients post sphincter sparing rectal resection surgery with LARS Syndrome.


Recruitment information / eligibility

Status Recruiting
Enrollment 62
Est. completion date October 1, 2025
Est. primary completion date February 1, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients 6-18 months post restorative surgery (either resection with a primary functional anastomosis or after the closure of a temporary ileostomy following curative surgery for rectal cancer) and, if applicable, at least one month post last adjuvant chemotherapy treatment - LARS score of 21 or greater - age 18 or older - able to read and write in Hebrew or English - able and willing to comply with the study requirements. Exclusion Criteria: - Chronic anal incontinence prior to surgery - inability to perform exercises due to cognitive or physical limitations - actively engaged in pelvic floor muscle exercises - pregnancy.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Paula Method of muscle exercises
12 weekly sessions of Paula Method of exercise

Locations

Country Name City State
Israel Hadassah Medical Organization Jerusalem
Israel Rabin Medical Center Petach Tikva

Sponsors (1)

Lead Sponsor Collaborator
Hadassah Medical Organization

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in LARS score Comparison of the change in LARS score from baseline to the completion of 12 weeks of the intervention (within and between groups). 12 weeks
See also
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