Evaluation and Treatment of Adhesive Capsulitis Using Non-invasive Neurostimulation Devices

Last updated: January 27, 2025
Sponsor: Université du Québec à Chicoutimi
Overall Status: Active - Recruiting

Phase

N/A

Condition

Bursitis

Treatment

Tendon vibration

Exercices

Tendon Vibration

Clinical Study ID

NCT06795932
CER-UQAC : 2025-1773
  • Ages > 18
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • 18 years old and over

  • Good general health

  • Adhesive capsulitis (experimental group) or

  • No shoulder pain (placebo group)

Exclusion

Exclusion Criteria:

  • 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.

Study Design

Total Participants: 30
Treatment Group(s): 3
Primary Treatment: Tendon vibration
Phase:
Study Start date:
October 17, 2024
Estimated Completion Date:
April 30, 2027

Connect with a study center

  • Lab BioNR - UQAC

    Saguenay, Quebec G7H 2B1
    Canada

    Active - Recruiting

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