跳至主要内容
临床试验/CTRI/2024/11/077340
CTRI/2024/11/077340尚未招募3 期

Spencer’s Muscle Energy Technique (SMET) versus Mulligan’s Mobilization With Movement (MWM) for persons with Adhesive Capsulitis of Shoulder joint.

Internal - fluid research grant1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年12月9日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
Shoulder Active and Passive ROM by Goniometer and Inertial Measurement Unit

研究概览

简要总结

Persons with shoulder adhesive capsulitis will be assessed for eligibility and will be included after a written consent. Following this baseline assessment will be done by the physical therapist (outcome assessor), who will be blinded to the group allocation. Baseline assessment will include health history and outcomes; measurement of shoulder range using universal goniometer and inertial measurement unit (IMU), pain using Numerical pain rating scale (NPRS), muscle power using modified Medical Research Council (mMRC), shoulder function by using Shoulder Pain and Disability Index (SPADI). After this the patients will be randomized using sequentially numbered, opaque, sealed envelopes (SNOSE) into two groups. The intervention for the two groups will be given by principal investigator (PI). One group will receive Spencer’s muscle energy technique (MET) and the control group will receive Mulligan’s mobilization with movement (MWM) for 5 days. Both the groups will receive conventional therapy in addition. Conventional therapy includes isometric shoulder exercises, capsular stretches, finger-ladder exercise, pulley-rope and wand exercise. At the end of 5 days the outcomes will be reassessed by the physical therapist (Outcome assessor). The data will be analyzed to compare the outcomes following Spencer’s MET and Mulligan’s MWM in persons with shoulder adhesive capsulitis. In addition, we are providing a home exercise program to the patients and the outcomes will be assessed at 3-month follow-up, to evaluate the effect of therapy at 3 months.

研究设计

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

入排标准

年龄范围
30.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Persons diagnosed as primary or secondary AC
  • Pain -NPRS (more than 4 out of 10), Intermittent night or resting pain
  • Pain occurring at end range of active and passive movements
  • Active and passive range restriction.

排除标准

  • Ligament or rotator cuff injuries or tears in shoulder joint
  • Fusion, Ankylosis, Osteoarthritis of shoulder joint
  • Metabolic Bone Disease
  • Neoplastic Disease
  • Malignancies affecting the shoulder region.

结局指标

主要结局

Shoulder Active and Passive ROM by Goniometer and Inertial Measurement Unit

时间窗: baseline | 5th day | 3rd month

次要结局

  • Pain, Numerical Pain Rating Scale (NPRS)(baseline)
  • Function, Shoulder Pain & Disability Index (SPADI)(baseline)
  • Muscle power, Modified medical research council grade (mMRC)(baseline)

研究者

发起方
Internal - fluid research grant
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Saheba Safique

Christian Medical College, Vellore

研究点 (1)

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