Status:
RECRUITING
Assessment of the Benefit of the Mobility Assistance System (SAM) on Transfer Independence for a Reimbursement Request
Lead Sponsor:
WINNCARE
Collaborating Sponsors:
Pôle Saint Hélier
Conditions:
no Specific Condition Targeted
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This is a randomized, cross-over, multi-center, intention-to-treat, open-label study to assess the impact of the SAM Ergonom light (SAM) device on independence when transferring from the supine to the...
Eligibility Criteria
Inclusion Criteria:
- Aged 18 and over
- Unable to transfer from lying to sitting independently
- Requiring technical assistance or the help or supervision of a third party
- Using a medical bed
- In-patient care for a minimum of 3 weeks in a medical or rehabilitation facility
- Having freely consented to participate
- Affiliated with a social security scheme or entitled to benefits
Exclusion Criteria:
- Non-consolidated spinal or pelvic fracture
- Degenerative shoulder
- Cardiovascular disorders caused by physical exertion
- Joint pain localized to dorsolumbar spine
- Behavioural disorders (opposition, agitation, dementia)
- Invalid patient (disability, low tonicity), agitated, not lucid (confused, disoriented) at risk of falling, requiring physical restraint with bed rails on medical prescription
- Functional inability to move independently
- Cognitive impairment affecting reliability of response to questionnaires
- Motor or algic incapacity of the 2 upper limbs not allowing the use of a technical aid (lifting frame or SAM) to ensure transfer from lying to sitting position in bed
- Patient less than 146 cm tall
- Patient weighing less than 30 kg or more than 200 kg
- Patient with a mattress incompatible with the OS'CARE device
- Mattress length less than 190 cm or greater than 200 cm, and width less than 85 cm or greater than 120 cm
In addition, vulnerable persons covered by articles L. 1121-5 to 8 and L. 1122-1-2 of the French Public Health Code are excluded from the study:
- Pregnant, parturient or breast-feeding women
- Persons deprived of their liberty by judicial decision (including guardianship, curatorship and safeguard of justice) or administrative decision
- Persons under psychiatric care or admitted to a health or social institution for purposes other than research.
- Person in an emergency situation unable to give prior consent
Key Trial Info
Start Date :
February 11 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
February 1 2026
Estimated Enrollment :
54 Patients enrolled
Trial Details
Trial ID
NCT06698653
Start Date
February 11 2025
End Date
February 1 2026
Last Update
August 1 2025
Active Locations (3)
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1
Centre Mutualiste de Rééducation et de Réadaptation Fonctionnelles (CMRRF) de Kerpape
Ploemeur, France, 56270
2
Fondation Ildys
Ploemeur, France, 56270
3
Pôle Saint Hélier
Rennes, France, 35000