- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07316725
the Effect of Virtual Reality Exercise on Selected Electrolytes Levels in Intradialytic Patients (VRE)
December 19, 2025 updated by: sarah mostafa mohamed, Cairo University
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.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
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
Study Type
Interventional
Enrollment (Estimated)
40
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: sarah mohamed, master
- Phone Number: 01149967455
- Email: sarahalsyed88@gmail.com
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Virtual Reality Exercise
Twenty patients will receive virtual reality exercise during dialysis sessions three times per weeks for 3 months (30 minutes of guided VR 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
the patients will receive standard care in the form of medical care
|
|
Active Comparator: standard care
Twenty patients will receive standard care during dialysis sessions three times per weeks for 3 months.
|
the patients will receive standard care in the form of medical care
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Serum Electrolyte Levels
Time Frame: up to three months
|
Measurements the level of sodium, potassium, calcium and phosphorus by venous blood sample. the normal value for Sodium: 135-145 mEq/L ,Potassium: 3.5-5.0 mEq/L, Calcium: 8.5-10.2 mg/dL, and Phosphorus: 2.5-4.5 mg/dL |
up to three months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
blood pressure
Time Frame: up to three months
|
A sphygmomanometer will be used to assess blood pressure with normal range 120/80
|
up to three months
|
|
oxygen saturation levels
Time Frame: up to three months
|
A pulse oximeter will be used to assess oxygen saturation level.
95-100% considered normal for healthy individuals
|
up to three months
|
|
functional exercise capacity
Time Frame: up to three months
|
6-Minute Walk Test will be used to assess functional exercises capacity
|
up to three months
|
|
exercise intensity
Time Frame: up to three months
|
The Rated Perceived Exertion (RPE) Scale will be used to assess exercise intensity.
it is a subjective 6-20 scale measuring exercise intensity, where 6 is no effort (rest) and 20 is maximum effort.
|
up to three months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
January 1, 2026
Primary Completion (Estimated)
June 1, 2026
Study Completion (Estimated)
June 1, 2026
Study Registration Dates
First Submitted
December 19, 2025
First Submitted That Met QC Criteria
December 19, 2025
First Posted (Actual)
January 5, 2026
Study Record Updates
Last Update Posted (Actual)
January 5, 2026
Last Update Submitted That Met QC Criteria
December 19, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Urogenital Diseases
- Pathologic Processes
- Male Urogenital Diseases
- Kidney Diseases
- Urologic Diseases
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Chronic Disease
- Disease Attributes
- Renal Insufficiency
- Pathological Conditions, Signs and Symptoms
- Renal Insufficiency, Chronic
- Health Services Administration
- Health Care Quality, Access, and Evaluation
- Motor Activity
- Movement
- Musculoskeletal Physiological Phenomena
- Musculoskeletal and Neural Physiological Phenomena
- Quality of Health Care
- Quality Indicators, Health Care
- Exercise
- Standard of Care
- Exergaming
Other Study ID Numbers
- P.T.REC/012/005982
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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