Therapeutic Exercise Programme to Improve the Functional Capacities, Depression and Anxiety of Patients with Chronic Kidney Disease During Haemodialysis Sessions.
NCT ID: NCT06883968
Last Updated: 2025-03-19
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
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ACTIVE_NOT_RECRUITING
NA
67 participants
INTERVENTIONAL
2024-06-10
2025-06-27
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Therapeutic exercise intervention
This group recibe one intervention demonstrated by a physiotherapist about therapeutic exercise to apply during hemodialysis session
Therapeutic exercise during hemodialysis session
Participants in the intervention group will receive a therapeutic exercise program during hemodialysis sessions at the hospital. The physiotherapist, after assessing the participant, will plan a program with the sets and number of repetitions for the prescribed exercises based on the participant's condition.
In this exercise program, the lower and upper extremities will be worked on with the aim of improving strength, balance, as well as contributing to the improvement of the participant's quality of life and mood.
Control group
No interventions assigned to this group
Interventions
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Therapeutic exercise during hemodialysis session
Participants in the intervention group will receive a therapeutic exercise program during hemodialysis sessions at the hospital. The physiotherapist, after assessing the participant, will plan a program with the sets and number of repetitions for the prescribed exercises based on the participant's condition.
In this exercise program, the lower and upper extremities will be worked on with the aim of improving strength, balance, as well as contributing to the improvement of the participant's quality of life and mood.
Eligibility Criteria
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Inclusion Criteria
* Treated for a minimum of 3 months with HD
* With clinical stability (good tolerance to sessions expressed as stable vital signs during the session)
* Voluntarily and with prior signed informed consent, have agreed to participate in the study
Exclusion Criteria
* Cardiovascular problems (unstable angina, uncontrolled arrhythmia, decompensated heart failure, pericarditis or myocarditis, severe untreated mitral or aortic stenosis)
* Uncontrolled arterial hypertension (SBP \> 200 mmHg and DBP \> 120 mmHg)
* Uncontrolled diabetes
* Severe neuropathies
* Acute systemic infection
* Severe renal osteodystrophy
* Stroke (cerebrovascular accident, transient ischemic attack)
ALL
No
Sponsors
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University of Vic - Central University of Catalonia
OTHER
Responsible Party
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Cristina Font
PhD in Comprehensive care and health services
Locations
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Department of Social Sciences and Community Health. Research Group on Methodology, Methods, Models and Outcomes of Health and Social Sciences . Faculty of Health Sciences and Welfare. University of Vic-Central of Catalonia, Vic 08500, Spain
Vic, Barcelona, Spain
Countries
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Other Identifiers
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ACTYREN-01
Identifier Type: -
Identifier Source: org_study_id
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