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临床试验/NCT03136250
NCT03136250已完成不适用

Effects of Autogenic and Reciprocal Inhibition, Muscle Energy Techniques in the Management of Mechanical Neck Pain

Foundation University Islamabad1 个研究点 分布在 1 个国家目标入组 78 人开始时间: 2017年4月11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
78
试验地点
1
主要终点
Neck Disability Index (NDI) - Change is being assessed

研究概览

简要总结

Neck pain is among the most common musculoskeletal disorders worldwide and is an important public health issue in terms of personal wellbeing. Prevalence of neck pain show excessive variations, with a point prevalence varying between 6% and 22%, and one year prevalence ranging between 1.5-75%. Neck pain like all other mechanical disorders leads to pain, disability and decreased range of motion (ROM). Stretching is a very common exercise performed by sportsmen, elderly, in physical therapy and rehabilitation patients, thus practiced in all sorts of fitness programs. The major types of stretching included in the literature are static, dynamic and pre-contraction stretching; of which static stretching is the conventional type of stretching. The different types of pre-contraction stretching include Proprioceptive Neuromuscular Facilitation (PNF) stretching, Post Isometric Relaxation (PIR), Post Facilitation stretch (PFS) and Active Isolated Stretch (AIS). Pre-contraction stretching is also considered a part of Muscle Energy Technique (MET). Recently MET and pre-contraction stretching have been shown to have significant superiority over conventional stretching in management of mechanical neck pain, but the evidence is currently lacking regarding which of the two pre-contraction stretching protocols, namely autogenic and reciprocal inhibition is more effective than the other. A RCT will be conducted in order to find and compare the effectiveness of conventional stretching and pre-contraction stretching (autogenic inhibition and reciprocal inhibition). One Control group (conventional group) and two Experimental groups (Experimental Group A - Autogenic Inhibition & Experimental Group B - Reciprocal Inhibition) will be formed. The participants will be recruited in the study if they meet the inclusion criteria using consecutive sampling from Fauji Foundation Hospital and randomized into the three respective groups. All the groups will receive the gold standard treatment for chronic neck pain including mobilization and modalities. In addition to the gold standard treatment the participants will receive specific stretching protocol based on their interventional group

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
Triple (Participant, Investigator, Outcomes Assessor)

盲法说明

The participant, investigator and outcome assessor are not aware of which treatment group the participant/patient is placed in.

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 to 70 years;
  • Neck pain on NPRS 4 to 8 (moderate cases);
  • Subacute or chronic cases (4 to 12 weeks).
  • Decreased or painful Cervical range of motion (CROM)

排除标准

  • Signs of serious pathology (e.g., malignancy, inflammatory disorder, infection);
  • History of cervical spine surgery in previous 12 months;
  • History of trauma or fractures in cervical spine;
  • Signs of cervical radiculopathy or myelopathy; and
  • Vascular syndromes such as VBI

研究组 & 干预措施

Group A (Control Group - Static Stretching)

Active Comparator

(Control Group - Static Stretching + Standard Treatment)

干预措施: Group A (Control Group - Static Stretching + Standard Treatment) (Other)

Group B (Autogenic Inhibition MET)

Experimental

(Autogenic Inhibition - PIR + Standard treatment)

干预措施: Group B (Autogenic Inhibition - PIR + Standard treatment) (Other)

Group C (Reciprocal Inhibition MET)

Experimental

(Reciprocal Inhibition - RI + Standard treatment)

干预措施: Group C (Reciprocal Inhibition - RI + Standard treatment) (Other)

结局指标

主要结局

Neck Disability Index (NDI) - Change is being assessed

时间窗: Pre-treatment (First day before treatment), Immediate Follow Up (After 1st treatment session) & Follow Up (After 5 days of Treatment)

to measure patient's pre and post functional disability

Cervical Range of Motion (CROM) - Change is being assessed

时间窗: Pre-treatment (First day before treatment), Immediate Follow Up (After 1st treatment session) & Follow Up (After 5 days of Treatment)

To measure patient's improvement in cervical range of motion

Cervical Isometric Muscle Strength (Modified Sphygmomanometer dynamometry) - Change is being assessed

时间窗: Pre-treatment (First day before treatment), Immediate Follow Up (After 1st treatment session) & Follow Up (After 5 days of Treatment)

To measure patient's improvement in Isometric Muscle Strength

Pain (Numeric Pain Rating Scale) - Change is being assessed

时间窗: Pre-treatment (First day before treatment), Immediate Follow Up (After 1st treatment session) & Follow Up (After 5 days of Treatment)

To measure the pre and post patient's perception of pain

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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