跳至主要内容
临床试验/NCT07834190
NCT07834190招募中不适用

Immediate Effects of Sustained Versus Oscillatory Mobilization in Patients With Thoracic Hypo-mobility

Foundation University Islamabad1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2026年2月13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
52
试验地点
1
主要终点
Thoracic Pain (T1-T12)

研究概览

简要总结

This randomized controlled trial compares two manual therapy interventions for adults with thoracic spine hypo mobility. Fifty-two participants are randomly allocated by coin toss to one of two equal groups (n = 26 each). Both groups first receive an identical preparatory protocol consisting of a combined session of TENS (transcutaneous electrical nerve stimulation) and hot pack application for 20 minutes, intended to reduce baseline pain and prepare the tissue for mobilization. Following this preparatory phase, Group A receives Maitland oscillatory mobilization, applied as small and large amplitude rhythmic passive movements directed at the spinous processes of the thoracic vertebrae (T1-T12). This is delivered as 3 sets of 15 repetitions, using Grades I-II to reduce pain and Grades III-IV to increase range of motion once pain has eased. Group B receives Kaltenborn sustained mobilization, which applies a slower, held stretch to the same thoracic spinous processes. This consists of 3 repetitions of a 30-60 second sustained hold, using Grades I-II for pain relief and Grade III (stretch beyond the point of restriction) to improve mobility once pain has decreased. Both interventions target the same spinal segments and are delivered in a single session by the same non-blinded protocol. Immediately after treatment, outcomes are reassessed: pain via the Numeric Pain Rating Scale (NPRS) and thoracic range of motion (flexion, extension, and right/left rotation in a lumbar-locked position) via a smartphone inclinometer application. The trial thus isolates the difference between a rhythmic, oscillatory mobilization technique and a slower, sustained-hold mobilization technique, allowing a direct immediate-effect comparison of the two manual therapy approaches for thoracic hypo mobility.

详细描述

Both intervention arms in this study address thoracic spine hypo mobility using manual mobilization techniques, but they differ fundamentally in the speed, rhythm, and mechanical strategy through which force is applied to the joint. Before either technique is applied, all participants in both groups receive an identical preparatory protocol: a combined 20 minute session of transcutaneous electrical nerve stimulation (TENS) and hot pack application. This preparatory phase serves to desensitize the local pain response and increase tissue extensibility, ensuring that any subsequent differences observed between groups can be attributed to the mobilization technique itself rather than to unequal baseline pain relief. Group A receives Maitland oscillatory mobilization, a passive accessory movement technique applied directly to the spinous processes of the thoracic vertebrae ranging from T1 through T12. The defining feature of this technique is its rhythmic, oscillatory character: the therapist applies small or large amplitude back and forth movements at a chosen point within or at the limit of the available range, rather than a single sustained push. Treatment is delivered as 3 sets of 15 repetitions per hypo mobile segment. The technique follows a graded progression. Grades I and II involve small amplitude oscillations performed well within the pain free range, and are used first, while pain remains elevated. These lower grades are believed to work primarily through neurophysiological pain modulation, stimulating mechanoreceptors that activate the spinal gating mechanism for pain, and through increasing the viscosity and circulation of synovial fluid within the facet joints, which may reduce joint stiffness. Once the participant's pain has decreased sufficiently, the therapist progresses to Grades III and IV, which are larger amplitude oscillations performed up to the end of the available range and into tissue resistance. These higher grades are intended primarily to produce mechanical effects, stretching peri-articular and capsular structures, thereby directly increasing thoracic range of motion rather than only modulating pain. Throughout the session, grade selection is adjusted according to the participant's real time pain response, so that pain relieving oscillations always precede range focused ones. Group B receives Kaltenborn sustained mobilization, applied to the hypo mobile T1-T12 spinous processes but using a fundamentally different mechanical approach: instead of rhythmic movement, the therapist applies a slow, sustained force and holds it at a chosen point in the range. This is delivered as 3 repetitions, each held for 30 to 60 seconds, with a brief rest between repetitions. As with Group A, treatment follows a graded, pain guided progression. Grades I and II involve a gentle sustained traction or glide that takes up the tissue slack without provoking pain, and are applied first. These lower grades are thought to act mainly through sustained stimulation of Type II mechanoreceptors, which are slow adapting joint receptors associated with reducing pain and muscle guarding, as well as through a general neurophysiological relaxation effect on the surrounding musculature. Once pain has eased, the therapist progresses to a Grade III sustained stretch, in which the joint is held beyond the point of tissue resistance for the full 30 to 60 second duration. This sustained end range hold is intended to produce a viscoelastic stretching effect on the joint capsule and surrounding connective tissue, gradually lengthening shortened structures and thereby increasing range of motion. Because the force is held rather than oscillated, this technique relies on sustained tissue creep over time rather than repeated movement to achieve its mechanical effect. In both groups, all mobilizations are performed manually by the treating therapist within a single treatment session, targeting identical spinal levels and using the same pain guided, low grade to high grade progression logic. The essential distinction lies in delivery: Group A's oscillatory technique relies on repeated rhythmic movement through the range, drawing primarily on neurophysiological gating and fluid dynamics, while Group B's sustained technique relies on a held end range stretch, drawing primarily on mechanoreceptor stimulation and viscoelastic tissue creep. This design allows the study to isolate whether the manner of force application i.e. oscillatory versus sustained, produces different immediate effects on pain and thoracic range of motion, even when the target tissue, dosage intensity, and preparatory protocol are held constant across groups.

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
None

入排标准

年龄范围
25 Years 至 44 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • adults (ages 25-44)
  • both male and female
  • localized thoracic pain (T1-T12)
  • Pain intensity of ≥ 3/10 on NPRS at baseline
  • reduced segmental mobility on PA spring test compared to adjacent segments
  • positive thoracic schober's test, indicating reduced thoracic mobility

排除标准

  • recent surgery (at least6 months ago) Diagnosed diseases
  • systemic diseases (e.g. RA, SLE etc)
  • spinal surgery
  • ankylosing spondylitis
  • recent history of fracture
  • scoliosis
  • spondylolisthesis and spondylosis
  • spinal TB
  • spinal stenosis
  • degenerative disc
  • fibromyalgia
  • malignancy

研究组 & 干预措施

Group B sustained mobilizations

Experimental

干预措施: Sustained Mobilizations (Procedure)

Group A oscillatory mobilizations

Experimental

干预措施: oscillatory mobilization (Procedure)

结局指标

主要结局

Thoracic Pain (T1-T12)

时间窗: Before and right after immediately the intervention.

Numeric Pain Rating Scale is an 11 point pain rating scale from 0-10 where 0 represents no pain and 10 represents the worst pain imaginable.

Thoracic Range of Motion

时间窗: Before and immediately after the intervention is applied.

Smartphone inclinometer will be used to assess the range of motion of the thoracic spine. The baseline assessment will establish each participant's pre-intervention ROM values, which will serve as the reference (baseline) values for subsequent comparison, changes in the thoracic ROM from baseline to post-intervention will be determined within each group.

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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