Effectiveness of 3D-MFR on Proprioception, Pain, ROM and Function in Cervical Spondylosis: A Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 36
- 试验地点
- 1
- 主要终点
- Neck proprioception using Joint repositioning error test, Pain using Visual analogue scale , Range of motion with Goniometer and Function using Neck disability index
研究概览
简要总结
Effectiveness of 3D-MFR on Proprioception, Pain, ROM and Function in Cervical Spondylosis : A Randomized Controlled trial
Aim of the study – To determine and compare the effect of 3D- MFR and sham release along with conventional physical therapy in Cervical Spondylosis.
Null hypothesis H0– There will be no difference in the effect of 3D- MFR and Sham release along with conventional physical therapy on neck proprioception, pain, ROM and function in Cervical Spondylosis.
Alternate Hypothesis H1- There will be difference in the effect of 3D- MFR and Sham release along with conventional physical therapy on neck proprioception, pain, ROM and function in Cervical Spondylosis.
Inclusion criteria- •Participants:1. of all gender aged between 25-65 years diagnosed radiologically with cervical spondylosis, 2. who report a pain intensity more than 3 on visual analogue scale, 3. willing to participate in the study
Exclusion criteria: •Participants with history of:1. psychological deficits hindering co-operation with treatment 2. neurological deficits (loss of sensations, paralysis) 3. active inflammatory conditions (rheumatic arthritis, ankylosing spondylitis) 4. contraindications to 3D-MFR like, Open wounds, previous neck surgery, cervical spine fracture, recent trauma, severe skin diseases like dermatitis.
A written informed consent will be obtained from the participants. A brief demographic data will be obtained from the subjects prior to the assessment. Baseline assessment of the participants will be done before the intervention. Then the participants will be divided into two groups i.e. Group A (n= 18) and Group B(n=18). Group A will be given 3D-MFR with conventional physical therapy and group B will be given Sham treatment and conventional physical therapy. Post- intervention data will be collected and analysed.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- None
入排标准
- 年龄范围
- 25.00 Year(s) 至 65.00 Year(s)（—）
- 性别
- All
入选标准
- •Participants:
- •of all gender aged between 25-65 years diagnosed radiologically with cervical spondylosis
- •who report a pain intensity more than 3cm on visual analogue scale
- •Â willing to participate in the study.
排除标准
- •Participants with history of:
- •psychological deficits hindering co-operation with treatment
- •neurological deficits (loss of sensations, paralysis)
- •active inflammatory conditions (rheumatic arthritis, ankylosing   spondylitis) 4.Contraindications to 3D-MFR like, Open wounds, previous neck surgery, cervical spine fracture, recent trauma, severe skin diseases like dermatitis.
结局指标
主要结局
Neck proprioception using Joint repositioning error test, Pain using Visual analogue scale , Range of motion with Goniometer and Function using Neck disability index
时间窗: At baseline after 2 weeks of treatment
次要结局
未报告次要终点
研究者
Bhakti Gauns
KAHER Institute of Physiotherapy