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WithdrawnNCT02904148ERIAMSUpdated Nov 26, 2019

Passive Mobilisation of Region of Shoulder Joints for Hemiplegic Patient

An interventional study of Shoulder mobilisation in Hemiplegia, sponsored by Centre Hospitalier Universitaire de la Réunion. Withdrawn. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2019-11-26.

Sponsored by Centre Hospitalier Universitaire de la Réunion · Not applicable, Interventional, and Supportive care

Why this study was withdrawn
No participants enrolled
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Not applicable
Ages
18 Years to 70 Years
Sex
All
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Study summary

Hemiplegia is a high prevalence pathology with 1 per 1000 habitants in France. One of these complications is shoulder pain which affects about 35 to 70% of cases. The medical care of this complication is critical because it affects the patient's quality of life and also hinders participation in rehabilitation sessions slowing the recovery of independence in activities of daily living.

Literature confirmed the involvement of the scapula in the hemiplegic shoulder pain with his attitude pronounced lateral rotation. But no data to confirm that passive mobilization reduce shoulder pain.

Because no data available to permit us to determine the sample size we set-up this preliminary study to check if efficiency found in these preliminary data are consistent with an estimable real efficacy in a randomized trial feasible.

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Conditions studied

  • Hemiplegia

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03

In context

Hemiplegia

374 studies on the registry are indexed under Hemiplegia; 83 are open to participants now.

Browse Hemiplegia studies →

Lead sponsor

Centre Hospitalier Universitaire de la Réunion is the lead sponsor of 137 studies on the registry; 35 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Hospitalized in Physical Medicine and Rehabilitation at Centre Hospitalier Universitaire Réunion (Site of Le Tampon)
  • Having made a cerebrovascular accident between 30 and 3 days before inclusion
  • with pain in the upper limb whose score with visual analogue scale is greater than or equal to 20 mm
  • able to understand the question: "Do you have arm pain?"

Exclusion criteria

Exclusion Criteria:

  • with visual analogue scale score lower than 20 mm at the inclusion
  • with aphasia of comprehension
  • with medical contraindication for passive shoulder mobilisation (Shoulder fracture, dislocation,...)
  • opposing to any mobilization
  • with shoulder pathology previously known
  • history of cerebrovascular accident prior 30 days before inclusion
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Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Shoulder mobilisation

    The shoulder mobilisation is performed daily by a physiotherapist for 45 days.

    Procedure: Shoulder mobilisation

Interventions

  • ProcedureShoulder mobilisation

    early shoulder mobilisation

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What researchers measure

Primary outcomes

  1. Pain evaluation with visual analogic scale

    Proportion of patients reducing by at least 20 mm their score on the visual analogic scale (VAS) from baseline Day 45

    Time frame: Change of pain evaluation between Day 0 and Day 45

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 26, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02904148
Lead sponsor
Centre Hospitalier Universitaire de la Réunion
Responsible party
Sponsor
First posted
Sep 16, 2016
Start date
Jan 2020 (estimated)
Primary completion
Apr 2022 (estimated)
Completion
Sep 2022 (estimated)
Last update
Nov 26, 2019

Study contacts

Andre Muller, MD
principal investigator · CHU de La Réunion

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Jul 2019. You cannot join it, but the record below documents what was studied.

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