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Passive Mobilisation of Region of Shoulder Joints for Hemiplegic Patient (ERIAMS)

C

Centre Hospitalier Universitaire de la Réunion

Status

Withdrawn

Conditions

Hemiplegia

Treatments

Procedure: Shoulder mobilisation

Study type

Interventional

Funder types

Other

Identifiers

NCT02904148
2015/CHU/09

Details and patient eligibility

About

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.

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

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

  • 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

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

Shoulder mobilisation
Experimental group
Description:
The shoulder mobilisation is performed daily by a physiotherapist for 45 days.
Treatment:
Procedure: Shoulder mobilisation

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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