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

NCT06173635 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 21

Last updated 2024-08-14

No results posted yet for this study

Summary

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.

Conditions

  • Healthy Volunteers

Interventions

DEVICE

Maxi Move 5

4 comparative devices will be used to evaluate the MM5 device

Sponsors & Collaborators

  • Loughborough University

    collaborator OTHER

  • Arjo AB

    lead INDUSTRY

Principal Investigators

  • Karin Hannander · Arjo AB

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-12-20
Primary Completion
2024-02-28
Completion
2024-05-31

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06173635 on ClinicalTrials.gov