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Combined Effect of Core Stability and Theraband Resisted Exercises on Gait Parameters in Lower Limb Burn

NCT07017764 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-06-11
Last updated
2025-06-12

Condition(s) studied

Burns

Investigational drug(s) / intervention(s)

Core stability exercisesTheraband resisted exercisesTraditional physical therapy program

Core stability exercises: Core stability exercises will be performed for 8 weeks, 3 times per week, 30 minutes per session. The program includes bed, wedge, and Swiss ball exercises. Bed exercises involve bridges, curl-ups, bird dog, and side bridges. Wedge exercises include curl-ups in various arm positions. Ball exercises involve bridges, curl-ups, bird dog, and push-ups. Each position is held for 7 seconds with 10 seconds of rest, repeated 10 times per set, for 2 sets per session with 60 seconds rest between sets.

Theraband resisted exercises: TheraBand resisted exercises will be performed for 8 weeks, 3 times per week, 30 minutes per session. Each session includes a 5-minute warm-up (stretching and joint mobilization), 30 minutes of resistance training for lower limbs (ankle, knee, hip), and a 5-minute cool-down with deep breathing and self-massage. Exercises include ankle flexion/extension, knee flexion/extension, and hip flexion/extension, abduction/adduction using elastic bands. Movements are done alternately on both sides, 10 reps each, 3 sets per session, with 1-2 min rest between sets. Yellow bands are used in weeks 1-4; green bands in weeks 5-8.

Traditional physical therapy program: All patients will receive a traditional physical therapy program consisting of ambulation training, stretching exercises for lower limb muscles, and range of motion exercises.

Study summary

The purpose of the study is designed to evaluate the combined effect of core stability and theraband resisted exercises on gait parameters in lower limb burn.

Eligibility

Sex
ALL
Min age
20 Years
Max age
40 Years
Healthy volunteers
No
Inclusion Criteria: * Patients will suffer from second degree lower limb burn (Partial thickness of thermal injury). * Total body surface area (TBSA) for the burns will be ranged from 20% to 25% . * Patients will begin the training program after complete skin closure from (1-2) weeks. * All patients enrolled to the study will have their informed consent. Exclusion Criteria: * Patients who had an open wound at or near treatment site. * Patients who had chemical or electrical burn. * Neurological and renal disorders. * Malignant conditions. * Psychiatric illness, severe behavior or cognitive disorders. * Use of neurological drugs that influence gait parameters. * History of lower extremity injuries with in the last 6 months. * History of muscular/ neural aliments (myopathy, myositis, peripheral neuropathy, muscular dystrophy). * Postural abnormality in the upper or lower extremities (such as kyphosis, lordosis, forward head, knee valgus and knee varus). * Surgery or fracture within a year before the study. * Insulin-dependent diabetes. * Joint rheumatoid arthritis. * Diagnosed cerebrovascular disease or any other disease that interferes with sensory input. * Lower extremity rotational deformities (increased anteversion, tibial torsion or pes planovalgus). * Hormonal changes.

Primary outcome measure(s)

  • Step length — 8 weeks
    Using two-dimentional (2D) videobased gait assessment system, the distance between the ipsilateral and contralateral heel strikes will be measured in meters before and after treatment for all participants in the three groups.
  • Stride length — 8 weeks
    Using two-dimentional (2D) videobased gait assessment system, the distance between two consecutive heel strikes of the same foot will be measured in meters before and after treatment for all participants in the three groups.
  • Step width — 8 weeks
    Using two-dimentional (2D) videobased gait assessment system, the distance between the centre lines of the two feet, perpendicular to the plane of walking will be measured in centimeters before and after treatment for all participants in the three groups.
  • Step time — 8 weeks
    Using two-dimentional (2D) videobased gait assessment system, the time between ipsilateral and contralateral heel strikes will be measured in seconds before and after treatment for all participants in the three groups.
  • Stride time — 8 weeks
    Using two-dimentional (2D) videobased gait assessment system, the time elapsed between the first contact of two consecutive footsteps of the same foot will be measured in seconds before and after treatment for all participants in the three groups.
  • Cadence — 8 weeks
    Using two-dimentional (2D) videobased gait assessment system, the number of steps in a minute, \[steps/ minute\]. It will be measured in seconds before and after treatment for all participants in the three groups.
  • Velocity — 8 weeks
    Using two-dimentional (2D) videobased gait assessment system, the distance covered by the body in unit time, (meter/minute) = Step length × Cadence. It will be measured in seconds before and after treatment for all participants in the three groups.

Trial sites (1)

FacilityCityRegionStatus
El Mahalla General Hospital and Burn Center in Mansoura University Hospital Al Mansurah Egypt
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07017764 on ClinicalTrials.gov ↗ ← All trials in Egypt