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Posture in Abdominopelvic Training in Women SUI

Posture Correction in Abdominopelvic Training in Women With Stress Urinary Incontinence

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03727945
Acronym
QoL SUI
Enrollment
49
Registered
2018-11-01
Start date
2014-09-30
Completion date
2016-09-30
Last updated
2018-11-01

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

Conditions

Female Stress Incontinence

Keywords

stress urinary incontinence, abdominopelvic exercise, quality of life

Brief summary

Measure effect of postural correction in abdominopelvic exercises on the improvement of the quality of life in patients with SUI. 42 women aged between 46-75 with SUI and stress-predominant mixed urinary incontinence. There were randomly assigned two groups of different treatment. Quality of life was measured by questionnaires: Incontinence Questionnaire Short Form (ICIQ-IU-SF) and King's Health Questionnaire (KHQ) global punctuation and incontinence impact. Treatment satisfaction was measured by VAS scale.

Detailed description

The aim of this study was compare the effect of postural correction in abdominopelvic exercises on the improvement of the quality of life in patients with stress urinary incontinence (SUI). Was a randomized 2-treatment parallel design study. The sample consist in 42 women aged between 46-75 with stress urinary incontinence (SUI) and stress-predominant mixed urinary incontinence (IUM). They were randomly assigned to two groups: Group 1 (n=21) who received abdomino-pelvic training, and Group 2(n=21) who received the above treatment, guidelines about postural correction. Both groups received 12 treatment sessions in first session information regarding clinical and demographical aspects will be collected. To evaluate results of postural correction combined with abdominopelvic exercise women was assessed:at initial session, post- intervention and 3 months post-intervention treatment.Quality of life was measured by spanish validation questionnaires: International Continence Questionnaire Short Form (ICIQ-IU-SF) and King's Health Questionnaire (KHQ) global punctuation and incontinence impact. Treatment satisfaction was measured by Visual analogic scale (VAS).

Interventions

OTHERabdominopelvic exercise and posture

n=21 women received supervised abdominopelvic exercise with previous postural correction. During 12 sessions a specialized physiotherapist supervised to realization of progressive abdominopelvic exercises, previous explain postural correction pelvis, cervical and dorsal zone.

OTHERabdominopelvic exercise

n=21 women received supervised abdominopelvic exercise. During 12 sessions a specialized physiotherapist supervised to realization of progressive abdominopelvic exercises.

Sponsors

University of Valencia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Urolog was not involved in physiotherapy treatment, randomised patients previous of treatment.

Intervention model description

2 aleatorized groups; control group (n=21) and intervention group

Eligibility

Sex/Gender
FEMALE
Age
45 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* SUI or stress-predominant mixed UI * diagnosed via clinical assessment and urodynamic study * Estrogenic deficit.: perimenopause, menopause, postmenopause

Exclusion criteria

* grade 3-4 prolapse, * functional alterations (Barthel Scale \> 85 points), * neurological or cognitive alterations (mini mental examination \> 24 points) * other predominant type of urinary incontinence.

Design outcomes

Primary

MeasureTime frameDescription
Changes from Quality of life. KHQbaseline,3 months,6 monthsThe questionnaire KHQ consists of 30 items distributed in 9 dimensions that we expose below, the scores of this questionnaire vary from 0 to 100, each item presents a scale type Likert with four options of response. The score of the KHQ questionnaire can be globally with a range of 0 (which indicates better health-related quality of life) at 100 points (indicating a worse quality of life)
Changes from Quality of life. ICIQ-IU-SFbaseline,3 months, 6 monthst consists of four questions that assess the presence of urge urinary incontinence, the amount of fluid evacuated and the involvement of the quality of life. The final score oscillates from 0-21, indicating higher scores to greater severity of the IU.
Treatment satisfaction3 monthsVisual analogic scale (VAS, 0-10, 0=minimum score, 10=maximum score). Higher values represent a better outcome (less treatment satisfaction)
Changes from IU impact. KHQbaseline,3 months, 6 monthsQuestion nº2 of KHQ measured IU impact in patient's life. Is a Likert scale 0-4 punctuation ( 0= no proceed, 4= A lot)
Changes from IU impact.ICIQ-IU-SFInitial,3 months, 6 monthsQuestion nº3 of ICIQ-IU-SF, measured IU impact in patient's life.Is a numeric scale (1-10),(1= none and 10= a lot )

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026