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

NCT ID: NCT07263243

Last Updated: 2025-12-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

26 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-01-24

Study Completion Date

2026-02-24

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Overweight , Obesity

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Study Group (Whole body vibration group)

The study group (no = 13) underwent single session of whole-body vibration (WBV) of using the PowerPlate device.

Group Type EXPERIMENTAL

Whole-body vibration device

Intervention Type 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.

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.

Group Type EXPERIMENTAL

Sham whole body vibration

Intervention Type OTHER

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.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

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.

Intervention Type DEVICE

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.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

25 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Cairo University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Rokaia Ali Zainelabedeen Mohamed Toson

Assistant Professor of Physical Therapy

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Jouf University

Jouf, , Saudi Arabia

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Saudi Arabia

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Rokaia Ali Toson Assistant Professor of Physical Therapy, Assistant Professor

Role: CONTACT

+2/01061259678

Nesma Morgan Allam, Assistant Professor

Role: CONTACT

+2 1281968332

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Rokaia Ali Toson, phD

Role: primary

+201061259678

Nesma Morgan Allam, PhD

Role: backup

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

7699

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Cavitaion vs W-BEMS on Central Obesity
NCT07307898 ACTIVE_NOT_RECRUITING NA
Shockwave Therapy (SWT)
NCT03986983 COMPLETED NA