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

Status: Recruiting
Location: See location...
Intervention Type: Device, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 25
Healthy Volunteers: t
View:

• 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).

Locations
Other Locations
Saudi Arabia
Jouf University
RECRUITING
Jouf
Contact Information
Primary
Rokaia Ali Toson Assistant Professor of Physical Therapy, Assistant Professor
Rokaiazain@yahoo.com
+2/01061259678
Backup
Nesma Morgan Allam, Assistant Professor
+2 1281968332
Time Frame
Start Date: 2026-01-24
Estimated Completion Date: 2026-02-24
Participants
Target number of participants: 26
Treatments
Experimental: Study Group (Whole body vibration group)
The study group (no = 13) underwent single session of whole-body vibration (WBV) of using the PowerPlate device.
Experimental: Control group (Sham whole body vibration group)
The sham WBV group (no=13) will stand on the same device with the vibtation shut off for single session.
Related Therapeutic Areas
Sponsors
Leads: Cairo University

This content was sourced from clinicaltrials.gov