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Recruiting NCT07263243

Immediate Effect of Whole-Body Vibration on Cardiovascular Response and Functional Capacity in Overweight/Obese Young Women

No phase Interventional Overweight , Obesity

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: Whole-body vibration device, Sham whole body vibration.
Who it may be relevant to
Registry conditions: Overweight , Obesity. Basic parameters: 18 years — 25 years · Female.
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
Saudi Arabia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Obesity has become a major global public health issue, defined by an excessive accumulation of body fat that presents substantial health risks. Over 650 million adults worldwide suffer from obesity, which is defined as having a Body Mass Index (BMI) of 30 or higher. Obesity is becoming more common in both developed and developing countries. Sedentary lifestyles, unhealthy eating habits that include processed foods and sugars, and genetic factors are the main causes of the rising prevalence of obesity. Obesity is a multifactorial condition that affects physical appearance and self-esteem, while also having significant implications for long-term health, leading to decreased life expectancy and lower quality of life.

Interventions

  • Device Whole-body vibration device
    Whole-body vibration (WBV) training using the Power Plate Pro 7HC (Northbrook, USA). The vibration frequency was set at 30 Hz, with an amplitude of 2 mm.
  • Other Sham whole body vibration
    A sham Whole body vibration will be used . participants will stand on the device without actual vibrations.This control condition will be used to isolate the effects of WBV from other potential influences such as standing posture and time spent on the the platform.

Primary outcome measures

  • Brachial blood pressure [Time frame: 1 day]
  • Heart rate [Time frame: 1 day]
  • Arterial O2 saturation [Time frame: 1 day]
Secondary outcome measures (2)
  • 6-Minute walk test [Time frame: 1 day]
  • The Borg scale [Time frame: 1 day]

Eligibility criteria

Inclusion criteria

  • Females aged 18 to 25.
  • normotensive (<140/90 mmHg).
  • Their BMI was from 25 to 40 kg/m2.
  • Sedentary (≤ 90min of regular exercise per week).

Exclusion criteria

  • Having previously diagnosed with any chronic disease.
  • Cardiorespiratory or neuromuscular conditions.
  • Participating in any exercise program.
  • Patients with a pacemaker.
  • Pregnancy.
  • Smoking.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Other

Study locations

Saudi Arabia · 1 center
  • Jouf University — Jouf

Identifiers

NCT: NCT07263243 · 7699

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗