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
NA
50 participants
INTERVENTIONAL
2023-01-01
2023-12-30
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.
Pelvic Floor Muscle Training on the Quality of Life in Women With Urinary Incontinence
NCT03514147
Pelvic Floor Muscle Contraction in Response to Different Verbal Instructions in Women With Urinary Incontinence
NCT03940794
Pelvic Floor Muscle Training in Treating Urinary Incontinence in Gynecologic Cancer Survivors
NCT01806350
The Relationship Between Pelvic Floor Muscle Function and Hip Pain Among Women
NCT06470620
Pelvic Floor Muscle Contraction Among Physiotherapy Students Before and After "Women Health" Course
NCT03917615
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Women who do not run at all, will begin running training protocol, and second evaluation will be performed following 2 months of training.
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.
NON_RANDOMIZED
PARALLEL
SCREENING
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
running group
women who run on a regular basis
runnin training program
gradual training program
control
women who do not run
runnin training program
gradual training program
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
runnin training program
gradual training program
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
The control group will recruit healthy women who do not physical active on a daily basis
Exclusion Criteria
* grade 3 or higher of pelvic organ prolapse.
18 Years
50 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Haifa
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Gali Dar
PHD, senior lecturer
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Gali Dar, Prof.
Role: PRINCIPAL_INVESTIGATOR
University of Haifa
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Haifa University, Department of PHysical Therapy
Haifa, , Israel
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.
170/22
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.