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Comparing Effects of Whole Body Vibration and Resisted Training on Quadriceps Strength After Lower Limb Burns

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

Lower Limb Burn
Muscle Weakness Condition

Treatments

Other: Resistance Exercise
Device: whole body vibration

Study type

Interventional

Funder types

Other

Identifiers

NCT06801301
P.T.REC/012/002762

Details and patient eligibility

About

Evaluate the therapeutic effect of Whole body vibration and Resistance training on strength of quadriceps post lower limb burn

Full description

Study Design:

This randomized controlled trial will include 60 patients suffering from partial thickness burns. The patients will be randomly divided into two equal groups, with each group consisting of 30 patients.

Study Explanation:

A verbal explanation about the importance of the study, its procedures, main aims, and conceptual approach will be provided to every patient.

Study Procedures:

The procedures of this study will be divided into two main categories: evaluation procedures and treatment procedures.

Evaluation Procedures:

Evaluation will be conducted using isokinetic dynamometry for all patients both before and after the study.

Treatment Procedures:

First Group: Patients in the first group will receive whole body vibration therapy.

Second Group: Patients in the second group will undergo resisted exercises.

Enrollment

60 patients

Sex

All

Ages

25 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

The subject selection will be according to the following criteria:

  • Age range between 25-40 years.
  • Male and female patients will participate in the study.
  • All patients have burn of 30% to 40%.
  • All patients have burn at lower limb
  • All patients have second degree burn
  • All patients have no chronic diseases.
  • All patients enrolled to the study will have their informed consent

Exclusion criteria

The potential participants will be excluded if they meet one of the following criteria:

  • Prosthesis;
  • Any neurological, musculoskeletal,or other chronic disease
  • Participation in an outside resistance training programs
  • Recent fracture or bone injury
  • Any medication that could affect strength adaptations and adversely affect the results of the study
  • Previous brain injury
  • Any disease affecting balance, vestibular or visual disorders
  • History of epilepsy.
  • Cardiac diseases.
  • Burn of sole of foot.
  • Exposed foot tendons.
  • Severe osteopathy.
  • Marked anemia (Ht<25%).
  • Serious peripheral vessel disease
  • Acute medical problem at study onset.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

group A
Experimental group
Description:
whole body vibration group
Treatment:
Device: whole body vibration
group B
Active Comparator group
Description:
resistance exercises
Treatment:
Other: Resistance Exercise

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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