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临床试验/NCT07844135
NCT07844135尚未招募不适用

Comparative Efficacy of Spencer's Technique Versus Mulligan's Technique on Pain, Range of Motion, and Quality of Life in Patients With Stage II Frozen Shoulder

Superior University2 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2026年10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
尚未招募
入组人数
72
试验地点
2
主要终点
Pain Intensity Assessed by Numeric Pain Rating Scale (NPRS)

研究概览

简要总结

Stage II frozen shoulder (adhesive capsulitis) is associated with pain, stiffness, restricted shoulder range of motion, and reduced quality of life. This randomized controlled trial will compare Spencer's Muscle Energy Technique with Mulligan's Mobilization with Movement in adults with Stage II idiopathic frozen shoulder. Seventy-two participants will be randomized to two groups of 36. Both groups will receive their allocated manual therapy together with conventional physiotherapy for four weeks, three sessions per week. Outcomes will be assessed at baseline and after the 4-week intervention using the Numeric Pain Rating Scale, goniometric shoulder range of motion, and the SF-36 questionnaire.

详细描述

The study is a two-arm, assessor-blinded randomized controlled trial. Eligible male and female participants aged 30 to 55 years with Stage II idiopathic frozen shoulder and pain for at least three months will be recruited from Ibn e Sina Hospital and Research Institute and City Hospital in Multan, Pakistan. Participants will be selected using non-probability convenience sampling and then randomized by chit-and-lottery method. Group A will receive Spencer's Muscle Energy Technique with conventional physiotherapy. Group B will receive Mulligan's Mobilization with Movement with conventional physiotherapy. The confirmed treatment schedule is three sessions per week for four weeks. Pain, shoulder range of motion, and health-related quality of life will be assessed at baseline and after the intervention.

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 (Outcomes Assessor)

盲法说明

Single-blind design: the outcome assessor will be blinded to participant group allocation.

入排标准

年龄范围
30 Years 至 55 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Male and female participants aged 30 to 55 years.
  • •History of idiopathic Stage II frozen shoulder.
  • •Experiencing shoulder pain for at least 3 months.

排除标准

  • •History of rotator cuff tears, rheumatoid arthritis, gouty arthritis, tumors of the shoulder region, or thoracic outlet syndrome.
  • •History of fracture of the upper limb involving the affected shoulder.

研究组 & 干预措施

Group A: Spencer's Technique

Experimental

Participants will receive Spencer's Muscle Energy Technique together with conventional physiotherapy three sessions per week for four weeks.

干预措施: Spencer's Muscle Energy Technique With Conventional Physiotherapy (Other)

Group B: Mulligan's Technique

Active Comparator

Participants will receive Mulligan's Mobilization with Movement together with conventional physiotherapy three sessions per week for four weeks.

干预措施: Mulligan's Mobilization With Movement With Conventional Physiotherapy (Other)

结局指标

主要结局

Pain Intensity Assessed by Numeric Pain Rating Scale (NPRS)

时间窗: Baseline and immediately after the 4-week intervention

Pain intensity will be assessed using the 11-point Numeric Pain Rating Scale from 0 (no pain) to 10 (worst imaginable pain).

Shoulder Range of Motion Assessed by Goniometer

时间窗: Baseline and immediately after the 4-week intervention

Shoulder flexion, abduction, and external rotation will be measured in degrees using a goniometer.

Health-Related Quality of Life Assessed by SF-36

时间窗: Baseline and immediately after the 4-week intervention

Health-related quality of life will be assessed using the 36-item Short Form Health Survey (SF-36). Domain scores are transformed to a 0 to 100 scale, with higher scores indicating better health status.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Muhammad Naveed Babur

Principal Investigator

Superior University

研究点 (2)

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