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临床试验/NCT06985836
NCT06985836招募中不适用

Effect of Mulligan Mobilization With or Without Niel Asher Technique on Pain, Range of Motion and Disability in Patients With Adhesive Capsulitis

Riphah International University1 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2024年12月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
42
试验地点
1
主要终点
Numerical Pain Rating Scale (NPRS)

研究概览

简要总结

Adhesive capsulitis is a prevalent condition characterized by pain and stiffness in shoulder joint and surrounding muscles shows decrease range and strength in patients with adhesive capsulitis. This study aims to determine the effect of mulligan mobilization with or without Niel Asher technique on pain, range of motion and disability in patients with adhesive capsulitis. This study will be a randomized controlled trial and will be conducted in Ibne-siena Hospital Multan and Multicare physiotherapy clinic. Non-probability convenience sampling will be used to collect the data. Sample size of subjects with age group between 40 to 60 years will be taken. Data will be collected from the patients having present complaint of adhesive capsulitis. Outcome measures used will be Numeric pain rating scale (NPRS) for shoulder pain and SPADI for shoulder disability and Universal Goniometer (GU) for Range of motion. An informed consent will be taken. Subjects will be selected on the basis of inclusion and exclusion criteria. Subjects will be divided into two groups by random number generator table. Both the Groups will receive heating pad, TENS. Group A will receive Mulligan Mobilizations and Neil Asher technique, and Group B will receive Mulligan mobilization and Conventional Treatment. Outcome measures will be measured at baseline and after 4 weeks. Data analysis will be done by SPSS version 26.

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
Single (Participant)

入排标准

年龄范围
40 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Age group 40-60 year
  • •Both gender male and female
  • •Stage 2 primary adhesive capsulitis with capsular pattern of restriction (rotation>abduction>flexion)
  • •Pain in shoulder should be ≤7 on NPRS
  • •Patient is willing to perform.

排除标准

  • •• Diabetes
  • •Malignancy
  • •Infection
  • •Arthoplasty
  • •Pregnancy
  • •Neurological disorders
  • •Thyroid diseases

研究组 & 干预措施

Mulligan Mobilization and Niel Asher technique

Experimental

Shoulder mobilization that includes:

  • Mulligan mobilization technique for shoulder external rotation and abduction as described by Mulligan. 3 sets of 10 repetitions with 1 minute rest between sets, 3 times a week for 4 weeks are performed
  • Niel Asher technique provided for 3 sessions a week for 4 weeks

干预措施: Mulligan Mobilization and Niel Asher technique (Other)

Mulligan Mobilization and Niel Asher technique

Experimental

Shoulder mobilization that includes:

  • Mulligan mobilization technique for shoulder external rotation and abduction as described by Mulligan. 3 sets of 10 repetitions with 1 minute rest between sets, 3 times a week for 4 weeks are performed
  • Niel Asher technique provided for 3 sessions a week for 4 weeks

干预措施: Mulligan Mobilization and Conventional physiotherapy. (Other)

Mulligan Mobilization and Conventional physiotherapy.

Active Comparator

Group B Will receive Baseline Physical therapy treatment and mulligan mobilization.

Standardized Physiotherapy treatment will be:

  • Modalities i.e. heating pad and TENS for ten Minutes
  • Postural correction exercises / Scapular retraction
  • Therapeutic Exercise : Codman' s, finger ladder, wand exercises
  • End Range Gleno-humeral joint stretching Both groups will come four times per week for a total of 4 weeks. Pre and post treatment values of both groups will be analyzed

干预措施: Mulligan Mobilization and Conventional physiotherapy. (Other)

结局指标

主要结局

Numerical Pain Rating Scale (NPRS)

时间窗: baseline and fourth week

Patient level of pain will be assessed using this scale. This scale ranges from 0 to 10. 0 indicates " no pain" and 10 indicates " worst pain" . NPRS have shown high test- retest reliability (r = 0.96 and 0.95, respectively)

Universal Goniometer (UG)

时间窗: baseline and fourth week

The range of motion will be measured using universal goniometer that has an inter-rater reliability (ICC2, 2 = 0.79 to 0.92) for shoulder.

Shoulder disability and shoulder Index SPADI

时间窗: baseline and fourthweek

The Shoulder Pain and Disability Index (SPADI) is a self-administered questionnaire that consists of two dimensions, one for pain and the other for functional activities. The pain dimension consists of five questions regarding the severity of an individual's pain. Functional activities are assessed with eight questions designed to measure the degree of difficulty an individual has with various activities of daily living that require upper- extremity use. The SPADI takes 5 to 10 minutes for a patient to complete and is the only reliable and valid region-specific measure for the shoulder. The reliability coefficient is ICC \>0.89 for Shoulder.

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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