跳至主要内容
临床试验/CTRI/2026/01/102096
CTRI/2026/01/102096尚未招募Phase 3 4

Effectiveness of Pulsed Muscle Energy Technique as compared with Scapular stabilization exercises on Functional Capacity, Pain and Quality of life in patients with Scapulocostal Syndrome – A Randomized Controlled Trial

P Aliver Justin1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年3月20日最近更新:

试验速览

阶段
Phase 3 4
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
1. Functional Performance: Measured by Shoulder Pain and Disability Index (SPADI)

研究概览

简要总结

This randomized controlled trial investigates the effectiveness of Pulsed Muscle Energy Technique (PMET) compared to Scapular Stabilization Exercises (SSE) on functional capacity, pain, and quality of life in patients with Scapulocostal Syndrome (SCS). Sixty participants aged 18 to 60 years, clinically diagnosed with SCS, will be recruited from the Physiotherapy Department at Dr. SMCSI Medical College. Participants will be randomly allocated into two groups: Group A (PMET) and Group B (SSE). The study aims to compare both interventions using validated outcome measures such as the Shoulder Pain and Disability Index (SPADI) for function, Numeric Pain Rating Scale (NPRS) for pain, and SF 36 for quality of life. Additional measures including Pain Pressure Threshold (PPT) and scapular range of motion will serve as secondary outcomes.

The PMET intervention involves rhythmic, submaximal isometric contractions of scapular stabilizer muscles, including the rhomboids and middle trapezius, applied in short pulses to release myofascial tension and improve scapular mobility. In contrast, the SSE program emphasizes motor control, muscle activation, and postural correction through progressive exercises targeting the serratus anterior and lower trapezius. Both interventions will be administered three times per week for six weeks, with evaluations conducted at baseline, two weeks, and six weeks. The study integrates artificial intelligence based tools such as Elicit, Scite AI, and Kinovea to support literature synthesis, data accuracy, and motion analysis, ensuring methodological precision and minimizing human error during data collection and analysis.

Data will be analyzed using SPSS version 29 with statistical significance set at p less than 0.05. Independent t tests and chi square tests will assess baseline comparability, while mixed model repeated measures ANOVA will examine within group and between group effects over time. AI assisted validation and double entry procedures will ensure data integrity, and blinding of assessors will minimize bias. This study aims to provide evidence based insights into the comparative efficacy of PMET and SSE in improving pain, functional performance, and overall quality of life in individuals with scapulocostal syndrome, guiding future physiotherapy interventions for scapulothoracic dysfunction.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Diagnosed with scapulocostal syndrome by using Scapular Compression Test: Stabilizing the scapula during movement can alleviate symptoms if scapular instability is contributing.
  • (Unilateral or Bilateral)
  • Presence of self-reported shoulder girdle dysfunction as indicated by a minimum score of 20% disability on the Shoulder Pain and Disability Index (SPADI).
  • Report a minimum pain intensity of 4 and maximum 8 on the Numeric Pain Rating Scale (NPRS) in the last 7 days.
  • willing to provide informed consent and adhere to the study protocol.
  • Participants with intact neuromuscular control and no evidence of upper motor neuron lesion.

排除标准

  • 1.Individuals with cervical radiculopathy, thoracic outlet syndrome, cervical spondylosis, or intervertebral disc pathology confirmed clinically.
  • 2.Patients presenting with rotator cuff injuries, adhesive capsulitis, subacromial impingement, or any post-traumatic shoulder pathology will be excluded, as these conditions may independently alter scapular mechanics.
  • 3.Patients who have received corticosteroid injections, or analgesic therapy within the past two weeks.
  • 4.Subjects with spinal deformities (e.g., scoliosis, kyphosis) or significant postural deviations that affect scapular alignment will not be included.
  • 5.Pregnant or lactating women, and individuals with systemic illnesses affecting musculoskeletal health (e.g., rheumatoid arthritis).

结局指标

主要结局

1. Functional Performance: Measured by Shoulder Pain and Disability Index (SPADI)

时间窗: Pre intervention, Post intervention, 2week follow up, 6 week follow up

2. Pain Intensity: Measured by Numeric Pain Rating Scale (NPRS, 0–10)

时间窗: Pre intervention, Post intervention, 2week follow up, 6 week follow up

次要结局

  • Secondary Outcomes:(1. Health-Related Quality of Life (QoL): Measured by Short Form-36 (SF-36))

研究者

发起方
P Aliver Justin
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Aliver Justin

Kerala University of Health Sciences

研究点 (1)

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