CClinicalTrials.gg
Not yet recruitingNCT06662552Updated Oct 29, 2024

Pulsed Electromagnetic Therapy Versus Whole Body Vibration on Quadriceps Strength Post Burn

An interventional study of whole body vibration using crazy fit machine and Pulsed electromagnetic field therapy in Pulsed Electromagnetic Field, Whole Body Vibration and Burns, sponsored by Cairo University. Not yet recruiting at 1 site in Egypt. Open to participants aged 25 Years to 40 Years. Per ClinicalTrials.gov, last updated 2024-10-29.

Sponsored by Cairo University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Apr 2025, 1 year 6 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
25 Years to 40 Years
Sex
All
01

Study summary

The purpose of the study is to evaluate which is more effective pulsed electromagnetic field therapy or whole-body vibration on quadriceps strength after chronic burn

Read the detailed description

Severe burn is associated with excessive muscle wasting and atrophy. Muscle wasting is defined as unintentional weight loss of 5%- 10% of muscle mass, and severely burned patients are reported to lose up to 25% of total body mass acutely. (Dirks et al., 2016). These are worsened by deconditioning (eg, prolonged bed rest, immobilization, and inactivity). (Baker et al., 2007).

Furthermore, the need of this study is developed from the lack in the quantitative knowledge and information in the published studies about the effect of pulsed electromagnetic field therapy and whole-body vibration on quadriceps strength after chronic burn.

This study will be designed to provide a guideline about the effect of pulsed electromagnetic field therapy and whole-body vibration on quadriceps strength after chronic burn

02

Conditions studied

  • Pulsed Electromagnetic Field
  • Whole Body Vibration
  • Burns

Browse trials for

03

In context

Burns

719 studies on the registry are indexed under Burns; 145 are open to participants now.

This study's planned enrollment of 30 is below the median of 40 across 524 interventional studies indexed under Burns.

Browse Burns studies →

Lead sponsor

Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.

Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
25 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Both sex.
  2. Their ages will be ranged from 25 to 40 years.
  3. Have second degree burn of 10 % to 25 %.
  4. Their body mass index (BMI) will not exceed 34.9 Kg/m2.
  5. All patients will be clinically and medically stable when attending the study.

Exclusion criteria

Exclusion Criteria:

  1. Unstable cardiovascular problems like arrhythmia and heart failure.
  2. Diabetes mellitus.
  3. Chronic chest disease.
  4. Patients on medications affecting muscle power as steroids.
  5. Auditory and visual problems.
  6. Pregnancy \& lactation.
  7. Patients with history of epilepsy.
  8. Clinically significant peripheral vascular disease.
  9. Musculoskeletal or neurological limitation to physical exercise.
  10. Any cognitive impairment that interferes with prescribed exercise procedures.
  11. Amputation of lower limb.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    whole body vibration group

    Fifteen patients will receive whole body vibration and traditional physical therapy program (splinting, stretching exercises, strengthening exercises and range of motion (ROM) exercises) on quadriceps muscle (3 times per week, for 6 weeks), plus medical treatment

    Device: whole body vibration using crazy fit machine · Other: traditional physical therapy program

  • Active comparator
    pulsed electromagnetic field (PEMF) group

    Fifteen patients will receive pulsed electromagnetic field (PEMF) and traditional physical therapy program (splinting, stretching exercises, strengthening exercises and range of motion (ROM) exercises) on quadriceps muscle (3 times per week, for 6 weeks), plus medical treatment.

    Device: Pulsed electromagnetic field therapy · Other: traditional physical therapy program

Interventions

  • Devicewhole body vibration using crazy fit machine

    It will be applied on the whole body All subjects will be asked to stand in a squat position on the vibration platform with the knees bent 90 this position will be chosen because the vertical sinusoidal accelerations of the vibration platform had to be damped by the different muscles around the joints of the lower extremity) ,at a frequency of 30 Hz, 5 - 30 minutes per day, 3 times per week, for 6 weeks, and the physiotherapist will be standing beside the patient

  • DevicePulsed electromagnetic field therapy

    EMSCULPT device (BTL Industries Inc., Boston, MA) based on HIFEM technology. It consists of an appliance, motorized bed and solenoids. The appliance will be connected to electrical mains supplying230Vat frequency of 50 or 60 Hz with earth connection, Intensity 0-100. It will be used in the treatment of patient in group "B". Subjects will be positioned in a supine position, and the treatment will be performed by placing the applicator centered over their thigh region (quadriceps muscle's area), for 15 minutes per day, 3 times per week for 6 weeks, the physiotherapist will be sitting beside the patient

  • Othertraditional physical therapy program

    In the form of splinting, stretching exercises, strengthening exercises and range of motion (ROM) exercises on quadriceps muscle 15 minutes per day, 3 times per week for 6 weeks.

06

What researchers measure

Primary outcomes

  1. Assessment of change on quadriceps muscle strength using hand-held dynamometer

    The study involves a bolster positioning to ensure a 35° knee flexion angle, verified using a goniometer. Participants are instructed to maintain their knee in contact with the bolster, with the dominant leg flexed at the hip and knee to stabilize the pelvis. Hips and buttocks are kept flat on the couch, and knee contact is maintained to maintain the angle. Participants are asked to push maximally against the pad to straighten their leg from the knee.

    Time frame: at baseline and after 6 weeks

07

Study locations

1 site
  • out-patient clinic, faculty of physical therapy, Cairo university
    Giza, Egypt
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 29, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06662552
Lead sponsor
Cairo University
Responsible party
Aya Talaat Moustafa Moustafa (principal investigator, Cairo University) — Principal investigator
First posted
Oct 29, 2024
Start date
Nov 5, 2024 (estimated)
Primary completion
Apr 5, 2025 (estimated)
Completion
May 5, 2025 (estimated)
Last update
Oct 29, 2024

Study contacts

Aya Talaat Mustafa, physical therapist
Contact
drayatalaat7@gmail.com
01112269937

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion