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临床试验/NCT06795932
NCT06795932招募中不适用

Prise En Charge Des Atteintes Proprioceptives Chez Une Population Avec Capsulite Rétractile

Université du Québec à Chicoutimi1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年10月17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
30
试验地点
1
主要终点
Shoulder Pain And Disability Index

研究概览

简要总结

The goal of this randomized controlled trial is to compare the integrity of somatosensory processing with transcranial magnetique stimulation (TMS) and corticospinal excitability of the affected shoulder in individuals with adhesive capsulitis versus healthy controls.

The secondary objective is to compare the clinical and neurophysiological effects of an intervention using tendon vibration (VIB) to induced kinesthetic illusions. This will involve comparing two groups: one receiving a real intervention versus a placebo intervention protocol, both coupled with standardized exercises in individuals with capsulitis. The hypotheses are that the proprioceptive processing and corticospinal excitability are impaired in the presence of capsulitis, and that the VIB + exercises intervention will result in greater improvements than the placebo VIB + exercises.

To goal is to establish the first empirical foundations for understanding adhesive capsulitis, using cutting-edge neurophysiological investigation technologies.

TMS will be used to explore the presence of maladaptive plasticity in motor networks by assessing the excitability and integrity of the primary motor cortex (M1) and the corticospinal tract.

Recruitement:

30 healthy participants and 30 participants with a diagnosis of adhesive capsulitis will undergo 2 baselines assesments, 6 interventions with tendon vibration and 2 follow-up evaluation. Participants will be age- and sex-matched.

Baseline and follw-up include:

  • Questionnaires : SPADI, QuickDASH, French version of the Mcgill Pain Questionnaire;
  • Active and passive range of motion;
  • Ultrasound for diagnosing capsulitis.

Comparison parameters:

  • active motor threshold (aMT)
  • Motor evoked potential (MEP) latency and amplitude
  • Standardized kinesthetic illusion procedure (SKIP) : direction of illusion, clearness, amplitude/speed.

Interventions :

  • 2 baselines including all questionnaires, ultrasound, active and passive range of motion, TMS procedure and SKIP;

  • 2 VIB interventions per week, for 3 weeks

  • Real VIB : 80Hz of vibration to induce kinesthetic illusions,

  • Placebo VIB : 40Hz of vibration that does not induce kinesthetic illusions

  • 2 follow-up including all questionnaires, ultrasound, active and passive range of motion, TMS procedure and SKIP.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •18 years old and over
  • •Good general health
  • •Adhesive capsulitis (experimental group) or
  • •No shoulder pain (placebo group)

排除标准

  • •Cognitive disorders;
  • •Any neurological disease/injury affecting the upper limbs;
  • •History or diagnosis of muscle, tendon, or capsular tear;
  • •Shoulder surgery/prosthesis;
  • •Pregnant woman;
  • •Presence of metal in the skull or jaw;
  • •History of epilepsy.

研究组 & 干预措施

Tendon vibration and standardized exercise protocol

Experimental

Six interventions inducing kinesthetic illusions (20 minutes, 1 illusion/minute).

Two interventions per week, for three weeks. Accompanied by a daily exercise protocol.

干预措施: Tendon Vibration (Device)

Tendon vibration and standardized exercise protocol

Experimental

Six interventions inducing kinesthetic illusions (20 minutes, 1 illusion/minute).

Two interventions per week, for three weeks. Accompanied by a daily exercise protocol.

干预措施: Exercices (Other)

Tendon vibration without kinesthetic illusion and standardized exercise protocol

Sham Comparator

Six interventions not inducing kinesthetic illusions (20 minutes) Two interventions per week, for three weeks. Accompanied by a daily exercise protocol.

干预措施: Exercices (Other)

Tendon vibration without kinesthetic illusion and standardized exercise protocol

Sham Comparator

Six interventions not inducing kinesthetic illusions (20 minutes) Two interventions per week, for three weeks. Accompanied by a daily exercise protocol.

干预措施: Tendon vibration (Device)

结局指标

主要结局

Shoulder Pain And Disability Index

时间窗: at baseline 1 and follow-up 1 : 2 months

SPADI : Shoulder Pain And Disability Index Thirteen questions to quantify the level of difficulty, ranging from 0 to 10, based on pain and disability. Five questions assess pain (0 = no pain, 10= worst pain imaginable) and eight questions assess the level of difficulty in performing different tasks (0= no difficulty, 10=too difficult, need help).

Quick Disability of the Hand, Arm and Shoulder

时间窗: at baseline 1 and follow-up 1: 2 months

QuickDASH : Quick Disability of the Hand, Arm and Shoulder Allowing the calculation of a percentage ratio from 14 questions, using a visual analogue scale from 1 (no difficulty) to 5 (incapacity), on the effects of pain on daily life activities, work, and sports, in addition to associated symptoms such as paresthesia and sleep disturbances.

Questionnaire St-Antoine

时间窗: at baseline 1 and follow-up 1: 2 months

French version of McGill Pain Questionnaire. Subjectively assess the pain level with 16 questions on a scale from 0 (none) to 4 (extremely severe).

Range of motion

时间窗: at baseline 1 and follow-up 1: 2 months

Measuring the active and passive range of motion with a goniometer.

Standardized Kinesthetic Illusion Procedure

时间窗: at baseline 1/2 and follow-up 1/2 : 2 months (+/- 2 weeks)

Using the SKIP to evaluate: * Clarity: 0 = no illusion, 1 = vague, 2 = moderately clear, 3 = perfectly clear * Direction: using words * Speed/amplitude of illusion: using a visual analogue scale where participants mark a point on the line to represent the speed/amplitude (ranging between very slow/small to very fast/high)

Active motor threshold

时间窗: at baseline 1-2 and follow-up 1-2: 2 months (+/- 2 weeks)

The active motor threshold represents the intensity of stimulation (%) required to elicit measurable motor evoked potentials.

Amplitude of motor evoked potential

时间窗: at baseline 1-2 and follow-up 1-2: 2 months (+/- 2 weeks)

The measurement of the motor evoked potential amplitude (peak-to-peak) It corresponds to the amount of neurons stimulated at the central et peripheral levels, expressed in microvolts.

Latency of motor evoked potential

时间窗: at baseline 1-2 and follow-up 1-2: 2 months (+/- 2 weeks)

The measurement of the motor evoked potential latency in miliseconds. It represent the conduction time from the application of the stimuli over the cortex to the target muscle.

次要结局

  • Sociodemographic - age(at baseline 1 : 1 day)
  • Sociodemographic - Sex(at baseline 1: 1 day)
  • Sociodemographic - Weight(at baseline 1: 1 day)
  • Sociodemographic - Height(at baseline 1: 1 day)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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