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Effect of Whole-body Vibration Training in Patients With Renal Dialysis

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

Renal Dialysis

Treatments

Device: whole body vibration

Study type

Interventional

Funder types

Other

Identifiers

NCT07049718
whole body vibration training

Details and patient eligibility

About

To show the effect of whole-body vibration in physical performance in patients with renal dialysis.

Full description

By now, safety and efficacy of WBV has not been investigated in patients with ESRD. Therefore, we performed this exploratory study in hemodialysis patients in order to elucidate potential effects of whole-body vibration exercise on physical performance and various biochemical markers in this condition. WBV is extensively studied as a means to prevent microgravity and immobility associated muscle wasting and bone loss in space flight and it is getting increasingly popular even among elderly.

Whole-body vibration exercise (WBVE) is a novel exercise protocol designed to prevent the loss of muscle strength and bone mineralization during the immobility and weightlessness of space flight.

A situation similar to HD. Vibration exercise uses high-frequency vibration of muscle groups causing positive feedback of the spinal reflex arc and resulting in high levels of muscle contraction to motor unit recruitment. There can be multiple physiological benefits from vibration exercise, including cardiovascular effects, bone health and muscle strength.

The advantages of WBV result from the combination of hardly any physical stress for the participants, short duration of intervention and a comparatively high effectiveness. means of exercise that can also be offered to those patients unable or unwilling to perform conventional training.

Enrollment

60 patients

Sex

Male

Ages

60 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

All patients that will be included in this study will meet the following criteria:

  1. Body mass index (BMI) from 25.0 to 29.9 kg/m2.

  2. Quitting smoking for more than 3 months.

  3. Their age will be ranged from 60-70 years old.

  4. Clinically and medically stable.

  5. Hemodialysis treatment over at least 6 months before enrollment.

  6. Patients with CKD (systolic blood pressure < 140 mmHg diastolic blood pressure < 90 mmHg and heart rate < 80 bpm).

  7. The presence of kidney damage (i.e., albuminuria) or decreased kidney function (i.e. glomerular filtration rate (GFR) < 60 ml/min per 1-73 m2) for 3 months or more irrespective of clinical diagnosis.

Exclusion criteria

Patients will be excluded if they have:

  1. Patients with uncontrolled pulmonary disease.

  2. Patients with vascular severe complication as critical limb ischemia.

  3. Patients with unstable angina, uncontrolled cardiac arrhythmia, decompensated heart failure.

  4. Patients with severe musculoskeletal problems (e.g., severe knee osteoarthritis or post knee replacement surgeries).

  5. Any patients who missed more than two weeks of the program or want to terminate the program.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

whole body vibration group
Experimental group
Description:
Thirty male patients will receive whole body vibration twice / week for 12 weeks with duration from 30 to 60secound until reach 20 minutes and intensity begin from initially 5 HZ until reach 28 HZ gradually increase each 4 weeks in addition to medication (Red Blood Cell Stimulating Agents, Iron, Blood Pressure Medications, Phosphate Binders, Vitamins B and C, Calcitriol, Cinacalcet and Antibiotics).
Treatment:
Device: whole body vibration
control group
No Intervention group
Description:
Thirty male patients will receive their own medication only (Red Blood Cell Stimulating Agents, Iron, Blood Pressure Medications, Phosphate Binders, Vitamins B and C, Calcitriol, Cinacalcet and Antibiotics).

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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