跳至主要内容
临床试验/CTRI/2025/07/089927
CTRI/2025/07/089927Not Applicable不适用

Effectiveness of Abdominal Hollowing and Piriformis Stretching Exercises in Spondylolisthesis Patients

Ganesh Dey1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年7月1日最近更新:

试验速览

阶段
不适用
状态
Not Applicable
发起方
入组人数
60
试验地点
1
主要终点
Pain Intensity: Measured using the Dallas Pain Questionnaire (DPQ) at baseline and post-intervention (6 weeks).

研究概览

简要总结

This study aims to evaluate the effectiveness of abdominal hollowing and piriformis stretching exercises in managing symptoms of spondylolisthesis. The randomized controlled trial will involve 60 participants, who will be randomly assigned to either an experimental group receiving the exercises or a control group receiving standard physiotherapy treatment. The primary outcomes of the study include pain intensity, functional disability, and kinesiophobia. Data will be collected at baseline and after 6 weeks of intervention. The goal is to assess whether these exercises can significantly reduce pain, improve mobility, and decrease fear of movement in patients with spondylolisthesis.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Participants eligible for the study must meet the following criteria: Both male and female patients, regardless of age, diagnosed with spondylolisthesis through radiological examination of the lumbar spine (L1 to L5 segment).
  • Patients experiencing low back pain with or without leg pain, regardless of whether the condition is acute or chronic.
  • Participants willing to provide informed consent and participate in the full course of the study.

排除标准

  • Participants will be excluded from the study if they meet any of the following criteria: History of spinal surgery, especially those with spinal fixation, as they may not respond to physiotherapy.
  • Any prior exercise therapy for back pain in the last 2 months, as this may affect the response to the interventions.
  • Presence of any neurological disorders that could interfere with participation or the treatment outcomes.
  • Patients with conditions other than spondylolisthesis causing back pain.
  • Pregnant women, as certain exercises may be contraindicated during pregnancy.
  • Diagnosed with spinal tumors, tuberculosis, or other systemic diseases contraindicated for physiotherapy.
  • Severe psychological disorders that may hinder the patient’s ability to comply with the exercise regimen.
  • Lack of cooperation, motivation, or dissatisfaction with the treatment protocol.

结局指标

主要结局

Pain Intensity: Measured using the Dallas Pain Questionnaire (DPQ) at baseline and post-intervention (6 weeks).

时间窗: 6 weeks of treatment (18 sessions).

Functional Disability: Assessed with the Oswestry Disability Index (ODI) at baseline and post-intervention (6 weeks).

时间窗: 6 weeks of treatment (18 sessions).

Kinesiophobia (Fear of Movement): Measured using the Tampa Scale for Kinesiophobia (TSK) at baseline and post-intervention (6 weeks).

时间窗: 6 weeks of treatment (18 sessions).

次要结局

  • Improvement in Spinal Mobility: Measured by range of motion tests (not detailed in the thesis, but typically assessed during the intervention period).

研究者

发起方
Ganesh Dey
申办方类型
Other [self-funded]
责任方
Principal Investigator
主要研究者

Ganesh Dey

Bangladesh Health Professions Institute (BHPI)

研究点 (1)

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