Passive Mobilisation of Region of Shoulder Joints for Hemiplegic Patient

Measurement of the Analgesic Efficacy of Shoulder Mobilization in Hemiplegic Patients

Status

Withdrawn

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02904148

Acronym

ERIAMS

Enrollment

Registered

2016-09-16

Start date

2020-01-31

Completion date

2022-09-30

Last updated

2019-11-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemiplegia

Brief 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.

Interventions

PROCEDUREShoulder mobilisation

early shoulder mobilisation

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

SUPPORTIVE_CARE

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 70 Years

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

Design outcomes

Primary

Measure	Time frame	Description
Pain evaluation with visual analogic scale	Change of pain evaluation between Day 0 and Day 45	Proportion of patients reducing by at least 20 mm their score on the visual analogic scale (VAS) from baseline Day 45

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026