NCT06578221

Brief Summary

This study was planned as a randomized controlled trial to investigate the effects of Kegel pelvic floor muscle exercises on urinary retention and comfort levels of patients after lumbar disc herniation surgery.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
58

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Aug 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 14, 2024

Completed
Same day until next milestone

Study Start

First participant enrolled

August 14, 2024

Completed
15 days until next milestone

First Posted

Study publicly available on registry

August 29, 2024

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 22, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 22, 2026

Completed
Last Updated

April 28, 2026

Status Verified

April 1, 2026

Enrollment Period

1.7 years

First QC Date

August 14, 2024

Last Update Submit

April 22, 2026

Conditions

Keywords

Nursesİntervertebral DiscComfortPatient Urinary RetentionSurgery

Outcome Measures

Primary Outcomes (1)

  • Effect of Kegel pelvic floor muscle exercises on urinary retention of patients after lumbar disc herniation surgery.

    Kegel pelvic floor muscle exercises will affect the urinary retention of patients after lumbar disc herniation surgery. Urinary retention will be evaluated using the Postoperative Data Collection Form developed by the researchers based on the literature. This form includes items assessing signs and symptoms of urinary retention within the first 8 hours postoperatively, such as pressure in the lower abdomen, pain in the lower abdomen, feeling of restlessness, and desire to urinate within 8 hours. Each symptom is assessed separately using the Visual Analog Scale (VAS).

    After completing Kegel pelvic floor muscle exercises in the first 8 hours after surgery.

Secondary Outcomes (1)

  • Effect of Kegel pelvic floor muscle exercises on comfort level after lumbar disc herniation surgery

    After completing Kegel pelvic floor muscle exercises in the first 8 hours after surgery.

Study Arms (2)

Kegel Pelvic Floor Muscle Exercise Group

EXPERIMENTAL

Kegel exercises will be performed by the researcher within the first 8 hours after being taken to the clinic room to perform the Kegel pelvic floor muscle exercises while in the supine position. Urinary retention and comfort level of patients will be evaluated after surgery.

Other: Kegel Pelvic Floor Muscle Exercise Group

Control Group

NO INTERVENTION

Urinary retention and comfort level of patients will be evaluated after surgery.

Interventions

After the surgery, the patients will be taken to the clinic room in a supine position and the researcher will perform the Kegel pelvic floor muscle exercises three times at the 1st, 4th and 7th hours within the first 8 hours after the patients are taken to the clinic room.

Kegel Pelvic Floor Muscle Exercise Group

Eligibility Criteria

Age18 Years+
Sexall(Gender-based eligibility)
Gender Eligibility DetailsHaving had surgery for lumbar disc herniation
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Agreeing to participate in the study
  • Over 18 years of age
  • No communication barrier
  • Having undergone lumbar disc herniation surgery under general anesthesia
  • Being immobile for the first 8 hours postoperatively
  • Not having a urinary catheter inserted during the intraoperative period

You may not qualify if:

  • Refusal to participate in the study
  • Previous urinary disorders/symptoms (such as Benign Prostatic Hyperplasia)
  • Spinal trauma, preoperative neurological disorder
  • Patients with preoperative catheterization

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Büşra Demirci

Ankara, University of Health Sciences, Turkey (Türkiye)

Location

Related Publications (6)

  • Huang BY, Leslie SW. Postoperative Urinary Retention. 2026 Feb 15. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan-. Available from http://www.ncbi.nlm.nih.gov/books/NBK549844/

    PMID: 31751034BACKGROUND
  • Wang R, Tunitsky-Bitton E. Short-term catheter management options for urinary retention following pelvic surgery: a cost analysis. Am J Obstet Gynecol. 2022 Jan;226(1):102.e1-102.e9. doi: 10.1016/j.ajog.2021.07.025. Epub 2021 Aug 5.

    PMID: 34363780BACKGROUND
  • Altschul D, Kobets A, Nakhla J, Jada A, Nasser R, Kinon MD, Yassari R, Houten J. Postoperative urinary retention in patients undergoing elective spinal surgery. J Neurosurg Spine. 2017 Feb;26(2):229-234. doi: 10.3171/2016.8.SPINE151371. Epub 2016 Oct 21.

    PMID: 27767680BACKGROUND
  • Aiyer SN, Kumar A, Shetty AP, Kanna RM, Rajasekaran S. Factors Influencing Postoperative Urinary Retention Following Elective Posterior Lumbar Spine Surgery: A Prospective Study. Asian Spine J. 2018 Dec;12(6):1100-1105. doi: 10.31616/asj.2018.12.6.1100. Epub 2018 Oct 16.

    PMID: 30322244BACKGROUND
  • Boulis NM, Mian FS, Rodriguez D, Cho E, Hoff JT. Urinary retention following routine neurosurgical spine procedures. Surg Neurol. 2001 Jan;55(1):23-7; discussion 27-8. doi: 10.1016/s0090-3019(01)00331-7.

    PMID: 11248301BACKGROUND
  • Boonstra AM, Schiphorst Preuper HR, Reneman MF, Posthumus JB, Stewart RE. Reliability and validity of the visual analogue scale for disability in patients with chronic musculoskeletal pain. Int J Rehabil Res. 2008 Jun;31(2):165-9. doi: 10.1097/MRR.0b013e3282fc0f93.

    PMID: 18467932BACKGROUND

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal İnvestigator

Study Record Dates

First Submitted

August 14, 2024

First Posted

August 29, 2024

Study Start

August 14, 2024

Primary Completion

April 22, 2026

Study Completion

April 22, 2026

Last Updated

April 28, 2026

Record last verified: 2026-04

Locations