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Core Stability as a Prognostic Factor of Urinary Incontinence in Patients Undergoing Robot-assisted Laparoscopic Prostatectomy

Core Stability as a Prognostic Factor of Urinary Incontinence in Patients Undergoing Robot-assisted Laparoscopic Prostatectomy

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05893394
Enrollment
62
Registered
2023-06-07
Start date
2023-03-01
Completion date
2023-11-30
Last updated
2023-06-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer

Brief summary

The study aims at investigating the possible correlation between core stability muscles and urinary incontinence following Robot-Assisted Laparoscopic Prostatectomy. Sixty-two patients who are candidates for Robot-Assisted Laparoscopic Prostatectomy will be enrolled. All participants will be asked to be evaluated in their core stability functionality 30-40 days before Robot-Assisted Laparoscopic Prostatectomy intervention. The core stability functionality result will be correlated with the urinary incontinence 45-50 days after intervention.

Detailed description

The study aims at investigating the correlation between core stability muscles and urinary incontinence following Robot-Assisted Laparoscopic Prostatectomy. All sixty-two participants will be asked to be evaluated in their core stability functionality 30-40 days before Robot-Assisted Laparoscopic Prostatectomy intervention. Core stability functionality will be evaluated through the Loumajoki Battery of tests, composed of 10 simple items in which the patients have to maintain core stability. In addition a Quality of Life questionnaire (WHO Quality of Life-BREF) will be administered. The core stability functionality result will be correlated with urinary incontinence measured by the 24h PAD test 45-50 days after intervention. At this point core stability will be evaluated again as done before.

Interventions

None listed

Sponsors

Istituto Clinico Humanitas
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Healthy volunteers
No

Inclusion criteria

* Patient who are candidates for Robot-Assisted Laparoscopic Prostatectomy * Objectivity of core muscles recruitment through the Loumajoki Battery

Exclusion criteria

* Pre-surgery incontinence * Pre-intervention radiotherapy treatment * Previous urogenital surgery * Concomitant presence of neurological, internal medicine or musculoskeletal system pathologies that may affect functional or motor recovery * Subjects with cognitive deficits and/or psychiatric disorders * Lumbar stabilization or abdominal interventions * Acute low back pain

Design outcomes

Primary

MeasureTime frameDescription
Correlation between Core stability functionality and Urinary Incontinence.Core stability evaluated 30-40 days before surgery. Urinary incontinence evaluated 45-50 days after surgeryTo evaluate any correlation between Core stability functionality measured with Loumajoki Battery and Urinary Incontinence measured with 24h PAD test.

Secondary

MeasureTime frameDescription
Correlation between Core stability functionality and Quality of Life.Core stability evaluated 30-40 days before surgery. Quality of Life evaluated 30-40 days before surgeryTo evaluate any correlation between Core stability functionality measured with Loumajoki Battery and Quality of Life measured with WHO Quality of Life-BREF.
Variation between Core stability functionality at base line and at follow-up.Core stability evaluated 30-40 days before surgery and 45-50 days after surgeryTo evaluate any variation between Core stability functionality at base line and at follow-up measured with Loumajoki Battery.

Countries

Italy

Contacts

Primary Contactroberto gatti
roberto.gatti@hunimed.eu0282245610

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026