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临床试验/NCT07322198
NCT07322198Enrolling By Invitation不适用

Effects of Gong's Mobilization With and Without Scapular High Lift on Shoulder Range of Motion and Functional Recovery in Adhesive Capsulitis; a Randomized Clinical Trial

University of Management and Technology Sialkot Pakistan3 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2026年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
发起方
入组人数
42
试验地点
3
主要终点
NUMERICAL PAIN RATING SCALE (NPRS)

研究概览

简要总结

This study aims to compare the effectiveness of Gongs Mobilization with and without scapular High-lift in the management of Adhesive Capsulitis, focusing on specific outcomes like pain, functional outcomes, and work productivity.

详细描述

This study will be a randomized controlled trial with a sample size of 42 participants, as calculated by the G power tool, with 5 % attrition rate, diagnosed with Adhesive Capsulitis. Subjects will be selected through non-probability convenient sampling based on inclusion and exclusion criteria, and randomly assigned into two groups, with 21 participants in each group. Group A will receive Gong mobilization with scapular high-lift, while Group B will receive Gong mobilization without scapular high-lift, both in conjunction with conventional therapy. Demographic Data will also be collected. Baseline and post-intervention data will be collected using SPADI, NPRS, and a goniometer. Data will be analyzed by using IBM SPSS 26.0. At the same time, the Shapiro-Wilk test will be applied to check normality.

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
否

入选标准

  • •Participants, including both males and females.
  • •aged 40 to 60 years.
  • •Diagnosed with unilateral Adhesive capsulitis at the 2nd or 3rd stage of the disease

排除标准

  • •History of any trauma, tumor, fracture, surgery, or infection in a shoulder joint.
  • •Patient with pregnancy and a history of abnormal neurological status (radiculopathy, stroke with hemiplegia, brachial plexus injury).
  • •Restricted shoulder due to burns or postoperative scars.
  • •Moderate or High levels of diabetes.

研究组 & 干预措施

GROUP B (GONG'S MOBILIZATION WITHOUT SCAPULAR HIGHLIFTS)

Experimental

GROUP B (GONG'S MOBILIZATION WITHOUT SCAPULAR HIGHLIFTS) containing 21 participants who were given Gong's mobilization without scapular high lifts for 30 minutes along with the conventional physiotherapy

干预措施: Experimental: GROUP B (GONG'S MOBILIZATION WITHOUT SCAPULAR HIGHLIFTS) (Other)

GROUP A (GONG'S MOBILIZATION WITH SCAPULAR HIGHLIFTS)

Experimental

GROUP A (GONG'S MOBILIZATION WITH SCAPULAR HIGHLIFTS) containing 21 participants who will be given Gong's mobilization with scapular high lifts for 30 minutes along with the conventional physiotherapy.

干预措施: Experimental: GROUP A (GONG'S MOBILIZATION WITH SCAPULAR HIGHLIFTS) (Other)

结局指标

主要结局

NUMERICAL PAIN RATING SCALE (NPRS)

时间窗: 4 Weeks

It is a fundamental tool used to evaluate pain intensity and pain tolerance. Subjects can rate their pain from 0 (no pain at all) to 10 (pain as bad as it could be) to check whether the pain is acute or chronic. 42. The test-retest reliability coefficient, the intra-class correlation coefficient (ICC) for NPRS, is 0.74, and the minimal clinically important difference (MCID) is 1.1 points

次要结局

  • SHOULDER PAIN AND DISABILITY INDEX (SPADI)(4 Weeks)
  • UNIVERSAL GONIOMETERY:(4 Weeks)

研究者

发起方
University of Management and Technology Sialkot Pakistan
申办方类型
Other
责任方
Principal Investigator
主要研究者

Danyal Ahmad

Head Of Department (HOD)

University of Management and Technology Sialkot Pakistan

研究点 (3)

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