Actively Recruiting

Phase Not Applicable
Age: 60Years - 80Years
FEMALE
Healthy Volunteers
NCT06839040

Effects of a Multidisciplinary Intervention on Fall Risk and Urinary Incontinence in Older Women

Led by Fundación Universidad Católica de Valencia San Vicente Mártir · Updated on 2025-02-21

120

Participants Needed

1

Research Sites

46 weeks

Total Duration

On this page

Sponsors

F

Fundación Universidad Católica de Valencia San Vicente Mártir

Lead Sponsor

U

University of Valencia

Collaborating Sponsor

AI-Summary

What this Trial Is About

This will be a quantitative, quasi-experimental, and longitudinal study spanning 18 weeks of intervention, followed by a 24-week follow-up, scheduled to begin in January 2025. The primary objective of this study is to evaluate the effects of a multidisciplinary intervention comprising physiotherapy, physical exercise, and psychoeducation on fall risk and urinary incontinence in non-institutionalized older adult women aged 60 to 80 years. Participants will be randomly assigned to one of four groups: 1. A multicomponent exercise group with verbal instructions for pelvic floor exercises. 2. A multicomponent exercise group with verbal instructions for pelvic floor exercises and psychoeducation. 3. A multicomponent exercise group without verbal instructions for pelvic floor exercises. 4. A control group. Multicomponent exercise sessions will be conducted twice a week, while the psychoeducation group will participate in five group therapy sessions throughout the program. The variables to be analyzed include balance, strength, power, pelvic floor function, quality of life, and self-esteem.

CONDITIONS

Official Title

Effects of a Multidisciplinary Intervention on Fall Risk and Urinary Incontinence in Older Women

Who Can Participate

Age: 60Years - 80Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Woman, aged between 60 and 80 years.
  • Not having done physical exercise in the last 3 months.
  • Present urinary incontinence (stress, urge, or mixed) after clinical diagnosis.
  • Score greater than 90 on the Barthel Scale.
  • No pathologies or functional alterations limiting physical exercise.
  • No severe cognitive alterations or mild cognitive deficit (Global Deterioration Scale  2 or Mini Mental State Examination  25).
  • Able to walk without support products.
  • Willing to attend at least 80% of the sessions.
Not Eligible

You will not qualify if you...

  • Taking medication that could affect exercise performance or study variables.
  • Presence of grade II-IV uterine prolapses.
  • Clinical disease or syndrome (chronic or acute cardiovascular, neurological, respiratory, or musculoskeletal disorders) interfering with intervention or evaluation.
  • Visual and/or auditory impairments that hinder intervention or evaluation.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Escuela de Doctorado. Universidad Católica de Valencia San Vicente Mártir. (Doctoral School. Catholic University of ValenciaSan Vicente Mártir)

Valencia, Valencia, Spain, 46001

Actively Recruiting

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Research Team

E

ESTHER RAMOS CASTELLANO

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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