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临床试验/CTRI/2026/02/103229
CTRI/2026/02/103229尚未招募不适用

Effect of Calisthenic versus Aerobic Exercises on Pain, Muscle Endurance, Lumbar Lordosis and Quality of Life in Chronic Non-Specific Low Back Pain: A Randomized Clinical Trial

Analiz Da Costa Campos1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2026年2月17日

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
36
试验地点
1

研究概览

简要总结

This randomized clinical trial aims to compare the effects of calisthenic exercises and aerobic exercises on pain, trunk muscle endurance, lumbar lordosis, and quality of life in individuals aged 18–35 years with chronic non-specific low back pain. Low back pain is a major cause of disability among young adults, often associated with reduced physical activity, poor posture, and muscle deconditioning. Exercise therapy is recommended as a first-line conservative treatment; however, the relative effectiveness of different exercise modalities remains unclear. In this study, participants will be randomly allocated into two groups. Both groups will receive conventional physiotherapy including Hot Moist Pack and Interferential Therapy. Group A will additionally perform a progressive calisthenic exercise program focusing on core stability and bodyweight strengthening, while Group B will undergo a progressive stationary bicycle aerobic exercise program. Treatment will be provided three times per week for four weeks under supervision. Outcomes will be assessed at baseline and at the end of the intervention using the Numeric Pain Rating Scale, trunk endurance tests, pelvic inclinometer for lumbar lordosis, and the Modified Oswestry Disability Questionnaire. The findings of this trial are expected to help determine the more effective exercise-based rehabilitation approach for managing chronic non-specific low back pain in young adults.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 35.00 Year(s)(—)
性别
All

入选标准

  • Individuals of all genders aged 18–35 years.
  • Individuals diagnosed with chronic non-specific low back pain lasting for at least 3 months.
  • Pain intensity between 3 and 7 on the Numeric Pain Rating Scale (NPRS) at baseline.
  • Able to perform basic physical activity and follow exercise instructions.
  • Willing to participate and provide written informed consent.

排除标准

  • Specific spinal pathology (fracture, infection, tumor, inflammatory spondyloarthropathy).
  • Clinical spinal instability or significant segmental hypermobility on examination.
  • Neurological compromise or radiculopathy consistent with nerve-root compression.
  • Prior spinal surgery or recent major spinal trauma.
  • Severe cardiorespiratory disease or other medical contraindications to aerobic or exercise therapy.
  • Pregnancy or within six months postpartum.

研究者

发起方
Analiz Da Costa Campos
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Analiz Olinda Da Costa Campos

KAHER Institute of Physiotherapy, Belagavi

研究点 (1)

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