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CompletedNCT07896135Updated Oct 26, 2026

Effects of Hop-Stabilization Training on Postural and Functional Rehabilitation in Children With Lower-Limb Burns

An interventional study of Progressive Hop-Stabilization Training and Traditional physical therapy in Burn Injury, Postural Balance Disorders and Gait Impairment, sponsored by Qassim University. Completed at 1 site in Saudi Arabia. Open to participants aged 10 Years to 17 Years. Per ClinicalTrials.gov, last updated 2026-10-26.

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

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Apr 2026, registered Oct 2026).
Updated Oct 26, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
54
Allocation
Randomized
Ages
10 Years to 17 Years
Sex
All
01

Study summary

Children with severe burns affecting both lower limbs may experience persistent difficulties with balance, walking, and physical function. This randomized controlled trial investigated whether adding progressive hop-stabilization training to standard physical rehabilitation improves postural control, dynamic balance, gait, and lower-limb function.

Fifty-four children aged 10-17 years with healed bilateral lower-limb burns were randomly assigned to two groups. Both groups received standard rehabilitation three times weekly for eight weeks, while the experimental group additionally performed supervised hop-stabilization exercises. Postural stability, dynamic balance, walking ability, and lower-limb functional performance were assessed before and immediately after treatment.

Read the detailed description

Children with lower-limb burns may experience persistent limitations in balance, gait, and lower-limb function. Hop-stabilization training provides repeated multidirectional loading, controlled landing, and rapid postural adjustment and may therefore represent a task-specific rehabilitation strategy; however, its effects in pediatric burn rehabilitation remain unclear. This two-arm, parallel-group randomized controlled trial will include 54 children aged 10-17 years with healed bilateral lower-limb burns and total body surface area involvement >30%. Participants will be randomly allocated in a 1:1 ratio to either a hop-stabilization group receiving progressive hop-stabilization training in addition to traditional physical therapy or a control group receiving traditional physical therapy alone. Both groups will receive treatment three times weekly for 8 weeks. The experimental program will include progressive multidirectional hopping and landing-stabilization exercises. Outcomes will be assessed at baseline and after treatment by a blinded examiner.

02

Conditions studied

  • Burn Injury
  • Postural Balance Disorders
  • Gait Impairment

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Keywords

  • Burns
  • Children
  • Hop-stabilization training
  • Balance
  • Gait
  • Lower-limb function
  • Rehabilitation
03

In context

Burns

731 studies on the registry are indexed under Burns; 146 are open to participants now.

This study's enrollment of 54 is above the median of 40 across 534 interventional studies indexed under Burns.

Browse Burns studies →

Lead sponsor

Qassim University is the lead sponsor of 50 studies on the registry; 7 are open to participants now.

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

04

Who can participate

Ages eligible
10 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Children aged 10-17 years.
  2. Healed deep partial-thickness, full-thickness, or mixed-depth burns involving both lower limbs.
  3. Total body surface area (TBSA) affected by burns greater than 30%.
  4. At least six months elapsed since hospital discharge.
  5. Medically stable and capable of participating in structured exercise rehabilitation.
  6. Able to walk independently without assistive devices.
  7. Able to understand and safely perform the required exercise and assessment procedures.

Exclusion criteria

Exclusion Criteria:

  1. Pre-existing neurological or musculoskeletal disorders that could affect balance, gait, or lower-limb performance.
  2. Metabolic diseases or peripheral neuropathy that could interfere with functional assessments.
  3. Visual or vestibular impairments affecting postural stability.
  4. Severe lower-limb contractures or restricted joint mobility that could compromise safe hopping or functional testing.
  5. Cognitive or behavioral difficulties that substantially limit understanding of instructions or adherence to study procedures.
  6. Concurrent participation in another structured rehabilitation or exercise program that could influence the study outcomes.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
54 participants (actual)

Study arms

  • Experimental
    Hop-Stabilization Training (HS-TR)

    Participants received an eight-week progressive hop-stabilization training program in addition to standard physical rehabilitation. Training was supervised by a physiotherapist and conducted three times weekly.

    Other: Progressive Hop-Stabilization Training · Other: Traditional physical therapy

  • Active comparator
    Standard Physical Rehabilitation

    Participants underwent supervised standard physical rehabilitation three times weekly for eight weeks.

    Other: Traditional physical therapy

Interventions

  • OtherProgressive Hop-Stabilization Training

    In addition to traditional physical therapy, participants in the experimental group received a progressive hop-stabilization training program three times per week for eight consecutive weeks. The program included side-to-side hopping, forward-and-backward hopping, forward hop-and-stabilization, figure-8 hopping, zigzag hopping, and 4-square hopping. All exercises were performed under the direct supervision of a physiotherapist. Difficulty throughout the program was progressively, verbal feedback was provided throughout the hop-stabilization program to promote appropriate landing biomechanics.

  • OtherTraditional physical therapy

    Participants in both groups received a supervised traditional rehabilitative exercise program three times per week for eight consecutive weeks. The program was individualized according to each child's functional status, burn characteristics, and exercise tolerance. Each 50-60-minute session included warm-up, aerobic conditioning, progressive strengthening, functional training, scar management as indicated, and cool-down.

06

What researchers measure

Primary outcomes

  1. Postural Stability

    Postural stability and dynamic Limits of Stability (LOS) were assessed using the ProKin System. Across three maximum-effort trials with 60-second rest intervals, the software calculated: Mediolateral Excursion Limit (%), Anteroposterior Excursion Limit (%), Overall Excursion Area (mm2), Directional Control Index, and Trunk Displacement Angle (o), with the mean of three successful trials retained for statistical analysis.

    Time frame: Baseline (Pre-Intervention)

  2. Postural Stability

    Postural stability and dynamic Limits of Stability (LOS) were assessed using the ProKin System. Across three maximum-effort trials with 60-second rest intervals, the software calculated: Mediolateral Excursion Limit (%), Anteroposterior Excursion Limit (%), Overall Excursion Area (mm2), Directional Control Index, and Trunk Displacement Angle (o), with the mean of three successful trials retained for statistical analysis.

    Time frame: Week 8 (Post-Intervention)

  3. Lower Quarter Y-Balance Test (YBT-LQ)

    Dynamic balance was assessed using the Lower Quarter Y-Balance Test (YBT-LQ). Participants stood on one leg on the central platform and reached as far as possible with the contralateral leg in the anterior (AT), posteromedial (PM), and posterolateral (PL) directions while maintaining balance. The composite score for was calculated as: composite score (%) = \[AT + PM + PL maximal reach distances (cm)\] / \[3 × lower-limb length (cm)\] × 100.

    Time frame: Baseline (Pre-Intervention)

  4. Lower Quarter Y-Balance Test (YBT-LQ)

    Dynamic balance was assessed using the Lower Quarter Y-Balance Test (YBT-LQ). Participants stood on one leg on the central platform and reached as far as possible with the contralateral leg in the anterior (AT), posteromedial (PM), and posterolateral (PL) directions while maintaining balance. The composite score for was calculated as: composite score (%) = \[AT + PM + PL maximal reach distances (cm)\] / \[3 × lower-limb length (cm)\] × 100.

    Time frame: Week 8 (Post-Intervention)

Secondary outcomes

  1. Functional Gait Assessment Modified for Children

    Functional gait performance was assessed using the Functional Gait Assessment modified for Children (FGA-mC). The FGA-mC consists of 10-item assessment designed to evaluate higher-level gait performance under progressively challenging conditions. Higher scores indicate better functional gait performance.

    Time frame: Baseline (Pre-Intervention)

  2. Functional Gait Assessment Modified for Children

    Functional gait performance was assessed using the Functional Gait Assessment modified for Children (FGA-mC). The FGA-mC consists of 10-item assessment designed to evaluate higher-level gait performance under progressively challenging conditions. Higher scores indicate better functional gait performance.

    Time frame: Week 8 (Post-Intervention)

  3. Single Hop for Distance Test

    The Single Hop for Distance Test used to assess unilateral lower-limb functional performance, including forward propulsion and landing control. Hop distance was measured to the nearest 0.5 cm from the starting line to the posterior aspect of the heel at landing. To allow standardized comparisons, absolute hop distance (cm) was normalized to leg length and demonstrated as a percentage.

    Time frame: Baseline (Pre-Intervention)

  4. Single Hop for Distance Test

    The Single Hop for Distance Test used to assess unilateral lower-limb functional performance, including forward propulsion and landing control. Hop distance was measured to the nearest 0.5 cm from the starting line to the posterior aspect of the heel at landing. To allow standardized comparisons, absolute hop distance (cm) was normalized to leg length and demonstrated as a percentage.

    Time frame: Week 8 (Post-Intervention)

  5. Timed Up and Down Stairs Test

    Timed Up and Down Stairs Test was used to assess functional mobility. the subject was asked to stand 30 cm from the bottom of a 14-step flight of stairs (19.5-cm step height). The test score was the time in seconds from the "go" cue until the second foot returned to the bottom land

    Time frame: Baseline (Pre-Intervention)

  6. Timed Up and Down Stairs Test

    Timed Up and Down Stairs Test was used to assess functional mobility. the subject was asked to stand 30 cm from the bottom of a 14-step flight of stairs (19.5-cm step height). The test score was the time in seconds from the "go" cue until the second foot returned to the bottom land

    Time frame: Week 8 (Post-Intervention)

  7. Timed One-Legged Stance Test

    The Timed One-Legged Stance test was used to assess single-limb static balance and postural control. Timing began when the no stance foot left the floor and stopped if the participant removed the hands from the hips, looked down, touched the floor with the contralateral foot, or otherwise lost the test position. Performance was recorded in seconds, with longer times indicating better balance ability.

    Time frame: Baseline (Pre-Intervention)

  8. Timed One-Legged Stance Test

    The Timed One-Legged Stance test was used to assess single-limb static balance and postural control. Timing began when the no stance foot left the floor and stopped if the participant removed the hands from the hips, looked down, touched the floor with the contralateral foot, or otherwise lost the test position. Performance was recorded in seconds, with longer times indicating better balance ability.

    Time frame: Week 8 (Post-Intervention)

07

Study locations

1 site
  • Physical Therapy Outpatient Clinic, Prince Sattam bin Abdulaziz University
    Al Kharj, Riyadh Region, Saudi Arabia
08

References and documents

Publications

  • Patel KF, Rodriguez-Mercedes SL, Grant GG, Rencken CA, Kinney EM, Austen A, Hou C, Brady KJS, Schneider JC, Kazis LE, Ryan CM. Physical, Psychological, and Social Outcomes in Pediatric Burn Survivors Ages 5 to 18 Years: A Systematic Review. J Burn Care Res. 2022 Mar 23;43(2):343-352. doi: 10.1093/jbcr/irab225. PubMed 34922361 ↗
  • Jeschke MG, Herndon DN. Burns in children: standard and new treatments. Lancet. 2014 Mar 29;383(9923):1168-78. doi: 10.1016/S0140-6736(13)61093-4. Epub 2013 Sep 11. PubMed 24034453 ↗
  • Koljonen V, Laitila M, Rissanen AM, Sintonen H, Roine RP. Treatment of patients with severe burns-costs and health-related quality of life outcome. J Burn Care Res. 2013 Nov-Dec;34(6):e318-25. doi: 10.1097/BCR.0b013e3182779c90. PubMed 23702860 ↗
  • Santos E, Chacon KL, Shepler LJ, McMullen KA, Slavin MD, van de Rijn M, Kowalske KJ, Ryan CM, Schneider JC. Balance Impairment in the Burn Population: A Burn Model System National Database Study. Eur Burn J. 2024;5(3):238-248. doi: 10.3390/ebj5030023. PubMed 39309318 ↗
  • Basha MA, Elnaggar RK, Aloraini SM, Alsultan F, Alharbi A, Alqahtani A, El-Keblawy MM, Azab AR, Kamel FH. Trajectories of physical fitness following paediatric burn injury: A two-year longitudinal and predictive analysis. Clin Rehabil. 2026 Jun 16:2692155261459618. doi: 10.1177/02692155261459618. Online ahead of print. PubMed 42299688 ↗

Individual participant data

Plan to share: No

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 26, 2026
Show all 1 update
  1. Oct 26, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07896135
Lead sponsor
Qassim University
Collaborators
Prince Sattam Bin Abdulaziz University, Cairo University
Responsible party
Maged Basha (Associate Professor of Physical Therapy, Qassim University) — Principal investigator
First posted
Oct 26, 2026
Start date
Apr 6, 2026
Primary completion
Oct 15, 2026
Completion
Oct 17, 2026
Last update
Oct 26, 2026

Study contacts

Maged A. Basha, PhD
study chair · Maged A. Basha

Oversight

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

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