A Comparison Study of the Maxi Move 5 (MM5) Device

Arjo

Status: Completed

Conditions: Healthy Volunteers

Treatments: Device: Maxi Move 5

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT06173635

MaxiMove5-MACC-001-2023

Details and patient eligibility

About

This trial aims to evaluate the added improvements from a caregiver and patient benefit perspective.

The trial should identify the forces involved for the caregiver when manoeuvring the lift.

Enrollment: 21 patients

Sex: All

Ages: 18 to 85 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

For expert patient:

• ≥18 years

• Healthy male or female

• 80-100 kg

  24 healthy volunteers (caregivers) will be recruited. They will require a strong working knowledge of passive floor lifts and patient positioning with the use of loop and clip slings.

Exclusion criteria

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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21 participants in 1 patient group

Maxi Move 5

Other group

Description:

24 healthy volunteers will evaluate all 5 devices

Treatment:

Device: Maxi Move 5