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临床试验/NCT07590557
NCT07590557已完成不适用

Rebuilding Capacity With Plyometrics: A Novel and Potent Stimulus for Strength and Power, and Functional Performance in Pediatric Post-Burn Population

Qassim University1 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2024年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
62
试验地点
1
主要终点
Lower-Limb Muscle Strength

研究概览

简要总结

Pediatric burn survivors may experience persistent deficits in lower-limb strength, explosive power, and functional performance after hospital discharge. This randomized controlled trial evaluated whether a 12-week supervised plyometric training program improves lower-extremity muscle strength, power, and functional capacity compared with a standard exercise program in children and adolescents with severe burn injuries.

详细描述

This two-arm, parallel-group, single-blind randomized controlled trial included 62 pediatric burn survivors aged 10-18 years with severe burns involving ≥30% total body surface area and lower-limb involvement. Participants were recruited 6-12 months after hospital discharge and randomly allocated in a 1:1 ratio to either plyometric training or standard exercise.

Both groups received supervised exercise twice weekly for 12 weeks. The experimental group completed progressive plyometric exercises designed to enhance lower-extremity explosive power and dynamic functional mobility. The control group received standard post-discharge rehabilitation focused on flexibility, aerobic conditioning, mobility, and basic strengthening. Outcomes were assessed at baseline and immediately after the 12-week intervention by blinded assessors.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
10 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Children and adolescents aged 10-18 years at the time of enrolment.
  • History of severe burn injury involving ≥30% total body surface area (TBSA), with lower-extremity involvement.
  • Between 6 and 12 months post-hospital discharge.
  • Ability to understand study instructions and safely perform the prescribed exercise program.

排除标准

  • Pre-existing neurological or musculoskeletal disorders that may affect lower-limb function or study outcomes.
  • Severe lower-limb joint contracture limiting functional movement.
  • Cognitive impairment preventing understanding of instructions or reliable participation.
  • Participation in another structured exercise, rehabilitation, or physical therapy program outside the study protocol during the trial period.

研究组 & 干预措施

Plyometric Training Group

Experimental

Participants received a 12-week supervised plyometric training program, twice weekly, with each session lasting 45 minutes. Sessions included dynamic warm-up, progressive plyometric exercises targeting vertical and horizontal force production, and cool-down.

干预措施: Plyometric Training (Other)

Standard Exercise Group

Active Comparator

Participants received a 12-week supervised standard exercise program, twice weekly, with each session lasting 45 minutes. Sessions focused on flexibility, aerobic conditioning, mobility, and basic lower-limb strengthening.

干预措施: Standard Exercise Program (Other)

结局指标

主要结局

Lower-Limb Muscle Strength

时间窗: pre-intervention (Week 0)

Quadriceps and hamstring strength will be assessed using an isokinetic dynamometer. After standardized positioning, stabilization, warm-up, and familiarization, participants will perform five maximal reciprocal knee extension/flexion repetitions. The highest peak torque value (Nm) for hamstrings and quadriceps will be recorded.

Lower-Limb Muscle Strength

时间窗: immediately post-intervention (Week 12)

Quadriceps and hamstring strength will be assessed using an isokinetic dynamometer. After standardized positioning, stabilization, warm-up, and familiarization, participants will perform five maximal reciprocal knee extension/flexion repetitions. The highest peak torque value (Nm) for hamstrings and quadriceps will be recorded.

次要结局

  • Vertical Jump Height(pre-intervention (Week 0))
  • Vertical Jump Height(immediately post-intervention (Week 12))
  • Broad Jump Distance(pre-intervention (Week 0))
  • Broad Jump Distance(immediately post-intervention (Week 12))
  • Reactive Strength Index(pre-intervention (Week 0))
  • Reactive Strength Index(immediately post-intervention (Week 12))
  • Lower Extremity Functional Scale Score(pre-intervention (Week 0))
  • Lower Extremity Functional Scale Score(immediately post-intervention (Week 12))
  • Six-Minute Walk Test Distance(pre-intervention (Week 0))
  • Six-Minute Walk Test Distance(immediately post-intervention (Week 12))
  • Timed Up and Down Stairs Performance(pre-intervention (Week 0))
  • Timed Up and Down Stairs Performance(immediately post-intervention (Week 12))
  • 4×10-Meter Shuttle Run Time(pre-intervention (Week 0))
  • 4×10-Meter Shuttle Run Time(immediately post-intervention (Week 12))
  • Figure-of-8 Walk/Run Test Time(pre-intervention (Week 0))
  • Figure-of-8 Walk/Run Test Time(immediately post-intervention (Week 12))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Maged Basha

Associate Professor of Physical Therapy

Qassim University

研究点 (1)

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