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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04824287
Other study ID # 2018/61
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 10, 2018
Est. completion date May 5, 2020

Study information

Verified date March 2021
Source Ankara Yildirim Beyazit University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study was conducted to evaluate the effect of pelvic floor muscle exercises on bowel evacuation problems and quality of life in individuals after stoma closure.


Description:

Sample of study was calculated as 32 using G*Power Software (ver. 3.1.9.2) for 80% power and medium effect size (f=0.25) at 95% confidence level in line with the data of Lin et al. Participants were assigned to the experimental and control groups by the stratified block randomization method. The locks were assigned to layers using Microsoft Excel. The individuals in the experimental group received pelvic floor muscle exercises training from the researcher using the Roy Adaptation Model in addition to routine discharge training. The patients received a PFME training booklet prepared by the researcher. Face-to-face training was given to the individuals in the experimental group on the day before the operation, on the second and third postoperative days, and on the day of discharge. The training continued with phone calls at the first, second and third weeks and the first, second, third, and sixth months after the surgery. Data was collected a day before discharge, first, second, third, and sixth months after the surgery.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date May 5, 2020
Est. primary completion date May 5, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Being between the ages of 18 and 75, - Being literate, - Having a stoma due to colorectal cancer, - Having no previous anal trauma, - Having no anal surgery other than colorectal cancer surgery, - Having no congenital anorectal anomaly, - Having no neurological problem, - Having no physical disability, - Having no previous experience of PFMEs before the surgery, - Being cognitively able to answer questions Exclusion Criteria: - Wanting to leave the study, - Having had previous biofeedback and electrical stimulation therapy applications, - Having another stoma, - Not being reachable by phone.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
pelvic floor muscle exercise
pelvic floor muscle exercises training from the researcher using the Roy Adaptation Model in addition to routine discharge training Face-to-face training was given to the individuals in the experimental group on the day before the operation, on the second and third postoperative days, and on the day of discharge. The training continued with phone calls at the first, second and third weeks and the first, second, third, and sixth months after the surgery Patients practiced exercises 6 month after surgery

Locations

Country Name City State
Turkey Ankara Yildirim Beyazit University, Faculty of Health Sciences, Department of Nursing Ankara

Sponsors (1)

Lead Sponsor Collaborator
Dilek Aktas

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bowel Evacuation Habits evaluated with "Assessment Form for Bowel Evacuation Habits and Psychosocial Problems". This form was developed by the researcher. Patients answer the question yes or no 6 month
Primary Wexner Scale Score Wexner Scale used to evaluate fecal incontinence. Minimum point is "0" an maximum point is "20". A score of 1 or above indicates a fecal incontinence problem 6 month
Primary Psychosocial Problems evaluated with "Assessment Form for Bowel Evacuation Habits and Psychosocial Problems". This form was developed by the researcher. The form include questions about psychosocial problems related bowel evacuation problems Patient answer the questions yes or no 6 month
Primary Health-related Quality of Life evaluated with Short Form 36 (SF-36) Health-related Quality of Life Scale. This scale include 8 subdimensions. scale does not have a single total score: the score for each dimension is calculated separately. For each subdimension minimum point is 0 and maximum point is 100. Higher score indicate best quality of life 6 month
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