Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
153 participants
OBSERVATIONAL
2007-04-30
2007-11-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Telehealth in the Rehabilitation of Urinary Incontinence in Older Women
NCT06200922
Pelvic Floor Symptoms and Quality of Life in Elderly Women - a Population-based Pilot Study
NCT02338726
The Pelvic Floor Muscles Strength and Sexual Function in Primigravid and Non-pregnant Nulliparous
NCT02866292
Effectiveness of Pelvic Floor Muscles Training in Group for Women With Urinary Incontinence
NCT03500185
Intelligent Diagnosis and Treatment System for Pelvic Floor Dysfunction in Elderly Women
NCT06372340
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CROSSOVER
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
G2
G2 = control group (no incontinence)
No interventions assigned to this group
G1
G1 = urinary incontinence
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Urinary incontinence
Exclusion Criteria
58 Years
87 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Catholic University of BrasÃlia
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Catholic University of Brasilia
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Claudia EC Souza, Ms
Role: PRINCIPAL_INVESTIGATOR
Catholic University of brasilia
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
UC
BrasÃlia, Federal District, Brazil
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ucb123cestari
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.