- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03727945
Posture in Abdominopelvic Training in Women SUI (QoL SUI)
Posture Correction in Abdominopelvic Training in Women With Stress Urinary Incontinence
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.
Study Overview
Status
Conditions
Intervention / Treatment
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).
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: abdominopelvic exercise and posture
N=21 received supervised physiotherapy abdominopelvic exercise previous postural correction.
|
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.
|
|
EXPERIMENTAL: abdominopelvic exercise
N=21 received supervised physiotherapy abdominopelvic exercise.
|
n=21 women received supervised abdominopelvic exercise.
During 12 sessions a specialized physiotherapist supervised to realization of progressive abdominopelvic exercises.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes from Quality of life. KHQ
Time Frame: baseline,3 months,6 months
|
The 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)
|
baseline,3 months,6 months
|
|
Changes from Quality of life. ICIQ-IU-SF
Time Frame: baseline,3 months, 6 months
|
t 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.
|
baseline,3 months, 6 months
|
|
Treatment satisfaction
Time Frame: 3 months
|
Visual analogic scale (VAS, 0-10, 0=minimum score, 10=maximum score).
Higher values represent a better outcome (less treatment satisfaction)
|
3 months
|
|
Changes from IU impact. KHQ
Time Frame: baseline,3 months, 6 months
|
Question nº2 of KHQ measured IU impact in patient's life.
Is a Likert scale 0-4 punctuation ( 0= no proceed, 4= A lot)
|
baseline,3 months, 6 months
|
|
Changes from IU impact.ICIQ-IU-SF
Time Frame: Initial,3 months, 6 months
|
Question nº3 of ICIQ-IU-SF, measured IU impact in patient's life.Is a numeric scale (1-10),(1= none and 10= a lot )
|
Initial,3 months, 6 months
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- 1. Salinas Casado J, Díaz Rodríguez A, Brenes Bermúdez F, Cancelo Hidalgo MJ, Cuenllas Díaz A, Verdejo Bravo C. Prevalencia de la incontinencia urinaria en España. UROD A. 2010; 23 (1): 52-66. 2. Aguilar-Navarro SG, Incontinencia urinaria en el adulto mayor. Rev Enferm Inst Mex Seguro Soc. 2007; 15 (1): 51-56. 3. Zunzunegui Pastor MV, Rodríguez Laso A, García de Yébenes MJ, Aguilar Conesa M.D, Lázaro y de Mercado P y Otero Puime A. Prevalencia de la incontinencia urinaria y factores asociados en varones y mujeres de más de 65 años. Aten Primaria. 2003; 32 (6): 337-342. 4. Grosse D, Sengler J. Reeducación del periné fisioterapia en las incontinencias urinarias. Ed Masson. 2001. 5. Robles JE (editor). I Curso de formación en incontinencia urinaria. Pamplona: Newbook ediciones. 2001. 6. Guía clínica sobre la incontinencia urinaria. Schroder A, Abrams P. Andersson KE, Artibani W, Chapple CR, Drake MJ, Hampel C, Neisius A, Tubaro A, Thuroff JW. European Association of Urology. 2010. 7. Lacima G, Espuña M. Patología del suelo pélvico. Gastroenterol Hepatol. 2008; 31 (9): 587-595. 8. Sapsford R. The pelvic floor. A clinical model for function and rehabilitation. Physiotherapy. 2001; 87 (12): 620-630.
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- H1410616852782,
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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