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Use of Auriculotherapy for Urinary Incontinence in adults or elderly people who have undergone genital or urinary surgery

Efficacy of Auriculotherapy for Urinary Incontinence in adults or elderly people undergoing genitourinary surgical procedures: mixed methods study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-8p38sh3
Enrollment
Unknown
Registered
2024-06-12
Start date
2024-09-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Urinary incontinence stress

Interventions

This is a study with mixed methods, with a concomitant incorporated strategy, in which the quantitative stage will be developed through a quasi-experimental study, and the qualitative stage will be ex
have a manifestation of moderate, severe or very severe urinary incontinence, as classified using the urinary incontinence severity assessment questionnaire – Incontinence Severity Index
and, have preserved cognitive capacity, assessed through the Mini Mental State Examination. Those who meet the selection criteria will be invited to participate in the auriculotherapy sessions: eight
E02.190.044.133

Sponsors

Universidade Federal do Rio Grande
Lead Sponsor
Universidade Federal do Rio Grande
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adults or elderly people will be included; who undergo genitourinary surgery at a university hospital in southern Brazil; who are in the immediate post-operative period (between 24 hours and seven days) or late post-operative period (from the seventh post-operative day); have moderate, severe or very severe urinary incontinence, as classified using the urinary incontinence severity assessment questionnaire – Incontinence Severity Index; and, have preserved cognitive capacity, assessed through the Mini Mental State Examination

Exclusion criteria

Exclusion criteria: People who underwent treatment for urinary tract infections within 30 days of data collection; patients who require the use of an indwelling bladder catheter postoperatively

Design outcomes

Primary

MeasureTime frame
It is expected to find a reduction in moderate (3 to 6 points), severe (7 to 9 points) or very severe (10 to 12 points) levels of urinary incontinence, as assessed by the questionnaire to assess the severity of urinary incontinence (Incontinence Severity Index)

Secondary

MeasureTime frame
No secondary outcomes are expected

Countries

Brazil

Contacts

Public ContactOclaris Munhoz

Universidade Federal do Rio Grande

oclaris_munhoz@hotmail.com+55(55)996799013

Outcome results

None listed

Source: REBEC (via WHO ICTRP)