Comparison of Two Exercise Programmes in Patients Undergoing Hemodialysis
NCT ID: NCT02832440
Last Updated: 2017-04-05
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
60 participants
INTERVENTIONAL
2014-09-30
2017-01-31
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.
Home-based Exercise in Chronic Kidney Disease
NCT03621176
Effect of Intradialytic Resistance Versus Aerobic Exercise on Cardiovascular System in Patients on Regular Hemodialysis
NCT07054827
An Exercise Facilitator to Activate Simple Training Programs in the Dialysis Center
NCT04282616
Efficacy of an Intradialysis Combined Training Program on Disability Level and Physical Performance.
NCT02883309
Quantifying the Deterioration of Physical Function in Renal Patients
NCT02832466
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.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Intradialytic exercise
Exercise during hemodialysis
Exercise programmes
Home-based exercise
Exercise at home
Exercise programmes
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Exercise programmes
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* be medicable stable
* complete all the physical tests
Exclusion Criteria
* inferior limb amputation without artificial aids
* cerebral vascular disease (ictus, ischemic)
* disability to complete functional tests
18 Years
90 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Cardenal Herrera University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Eva Segura OrtÃ
Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Eva Segura OrtÃ
Role: PRINCIPAL_INVESTIGATOR
Lecturer in the Cardenal Herrera University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Universidad CEU Cardenal Herrera
Moncada, Valencia, Spain
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.
CEU Card Herrera
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.