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临床试验/CTRI/2025/02/080470
CTRI/2025/02/080470尚未招募不适用

Effect Of Spiral Line Soft Tissue Release On Clinical Outcomes Among Subjects With Degenerative Disease Of Knee: A Quasi Experimental Study.

Ms Batul1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年2月24日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
1. Knee Range of Motion

研究概览

简要总结

INTRODUCTION: Knee osteoarthritis is identified among the common causes of disability worldwide.

Therapist are more focused on strengthening the muscles around the knee rather than stretching it.

An increased number of empirical studies are being conducted on myofascial release in knee OA patients, and they state the equal importance of myofascial release.

Anatomical spiral line release is a type of effective hands on interactive method that provides stretching, compression and sustained pressure into the restricted areas of the fascia

The anatomic line release is based on the tensegrity principle, and hence, the entire line of fascia needs to be released instead of the single muscle to bring about complete and long-lasting relief of symptoms.

AIM: To Evaluate the effects of spiral line release on knee osteoarthritis subjects.

METHADOLOGY:

STUDY DESIGN: A Quasi experimental study

STUDY DURATION: 4 weeks

RANDOMISATION: Block randomization.

Method of generating random sequence: computer generated randomization.

Method of concealment: Sequentially numbered, sealed, opaque envelopes

Method of block randomization: block size is 4 and total blocks needed is 15.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant, Investigator, Outcome Assessor and Date-entry Operator Blinded

入排标准

年龄范围
45.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Diagnosed with knee osteoarthritis.
  • Pain score of more than 4 on visual analogue scale (VAS).
  • Sit to reach test restriction (1-15cm for men and 5-16cm for women).
  • Willingness to participate and provide informed consent.

排除标准

  • Severe Comorbidities affecting mobility (eg.
  • Severe cardiovascular disease, neurological disorders)
  • Recent knee surgery or trauma
  • Contraindications to manual therapy (eg severe Osteoporosis, active infections, recent fracture, open wounds, hypermobility, rheumatoid arthritis, malignancy)
  • Pregnant women.

结局指标

主要结局

1. Knee Range of Motion

时间窗: Baseline, at the end of 4th week, 6th week, 8th week, 12th week

2. Visual Analogue Scale

时间窗: Baseline, at the end of 4th week, 6th week, 8th week, 12th week

3. Knee Injury And Osteoarthritis Outcome Score (KOOS)

时间窗: Baseline, at the end of 4th week, 6th week, 8th week, 12th week

4. Sit to reach test

时间窗: Baseline, at the end of 4th week, 6th week, 8th week, 12th week

5. Pain pressure Algometer

时间窗: Baseline, at the end of 4th week, 6th week, 8th week, 12th week

次要结局

  • Physical Performance Test, Muscle Strength(Baseline, at the end of 4th week, 6th week, 8th week, 12th week)

研究者

发起方
Ms Batul
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Batul Patanwala

Sri Ramachandra Institute Of higher Education And Research (Deemed to be university)

研究点 (1)

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