Implementation of Supportive Sling Device in Adults Post-stroke for Prevention of Shoulder Compliā¦ (NCT04028999) | Clinical Trial Compass
CompletedNot Applicable
Implementation of Supportive Sling Device in Adults Post-stroke for Prevention of Shoulder Complications
France25 participantsStarted 2019-07-03
Plain-language summary
Upper limb (UL) impairment is a common deficit following stroke with only an estimated 20 per cent of patients recovering function.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Having suffered in the last 6 months maximum a first stroke responsible for hemiplegia.
* Finding a clinical 5mm appendix, or with shoulder pain requiring prescription a scarf.
* Boston Diagnostic Aphasia Examination (BDAE) \> 3.
* Consent of the patient
* Patient affiliated or benefiting from a social security scheme
Exclusion Criteria:
* Stroke recurrence, or stroke more than 6 months-old
* Patient already wearing a coaptation scarf
* Presence of lymphoedema, venous thrombosis of the upper limb
* Neoprene allergy
* Severe cognitive impairment: Mini-Mental State (MMS) \<15
* Patient being part of another care protocol
* Adult under the protection of justice, tutors or curators
* Pregnant or lactating woman.
What they're measuring
1
Evaluate the effects of the EO31 shoulder with Goal Attainment Scale (GAS) scale