the Effect of Virtual Reality Exercise on Selected Electrolytes Levels in Intradialytic Patients
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Virtual Reality Exercise, standard care.
- Who it may be relevant to
- Registry conditions: Chronic Kidney Diseases. Basic parameters: 20 years — 40 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
this study will be conducted to investigate the effect of Intra-Dialysis virtual reality exercise on selected electrolytes balance in patients with end stage renal disease.
Detailed description
Chronic Kidney Disease (CKD) is a progressive condition that often leads to end-stage renal disease, requiring dialysis. Patients undergoing hemodialysis frequently experience physical inactivity and electrolyte imbalances, which can adversely affect their health outcomes. Regular physical activity is crucial for maintaining muscle strength and physical function in CKD patients.Electrolytes play vital roles in various physiological functions, including muscle contraction, nerve transmission, and fluid balance. In end stage renal disease patients, imbalances can lead to serious complications, including: hyperkalemia, Hyponatremia, and hypocalcemia.VR has been employed in medicine to assist patients in recovering their motor and cognitive abilities. It has proven effective in enhancing physical functions such as posture, balance, and motor skills. When combined with physical exercise, VR has been shown to improve the functional abilities and quality of life of hemodialysis patients. For those with end stage renal disease patients, who experience discomfort during hemodialysis, VR offers a distraction that can reduce the perception of pain, fatigue, nausea, lightheadedness, and headaches, thereby facilitating smoother exercise continuity and enhancing overall adherence to rehabilitation activities. so this study will be conducted to assess the effect of Intra-Dialysis Virtual Reality Exercise on Selected Electrolytes Balance in Patients with End Stage Renal Disease
Interventions
- Other Virtual Reality Exercise
the patients will receive 30 minutes virtual reality exercise; (5 minutes warm Up stretching exercise - 20 minutes cycling exercise -5 minutes cool down stretching exercise) plus standard care - Other standard care
the patients will receive standard care in the form of medical care
Primary outcome measures
- Serum Electrolyte Levels [Time frame: up to three months]
Secondary outcome measures (4)
- blood pressure [Time frame: up to three months]
- oxygen saturation levels [Time frame: up to three months]
- functional exercise capacity [Time frame: up to three months]
- exercise intensity [Time frame: up to three months]
Eligibility criteria
Inclusion criteria
- Patients are diagnosed with end stage renal disease on regular dialysis.
- Their ages will be arranged from 20-40 years old.
- All patients are under medical control.
- Patients on regular dialysis more than 3 months.
Exclusion criteria
- Visual impairment.
- Severe cognitive impairment.
- Recent major surgery.
- Patients with sever musculoskeletal problems.
- Severe cardiovascular disease limiting exercise.
- Patients with Hemoglobin drop less than 9 g/dl
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07316725 · P.T.REC/012/005982