OptiMalisation and efficiency of the provision process of Assistive Technology devices for the ARM hand function (OptiMalisatie en doelmatigheid van het verstrekkingsproces van hulpmiddelen voor ARM- en handfunctie in Dutch)

• Conditions: (Neuro)muscular disorders, ALS, MS, cervical spinal cord injury, plexus lesion, CVA

• Registration Number: NL-OMON25706
• Lead Sponsor: ot applicable

Brief Summary

Planned

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 96

Inclusion Criteria

The study population consists of adults (18 years and older) with limited arm-hand function who may benefit from an AT device for arm-hand function and consider the use of such a device. The latter is operationally defined as trying out a dynamic arm support or robotic arm.
The study population consists of a heterogeneous group of people with various conditions.

Exclusion Criteria

A potential participant may not participate in the study if one of the following exclusion criteria applies:
- limitations experienced in the hand function, but no limitations experienced in the arm function
- not being entitled in any way to a dynamic arm support or a robot arm in accordance with the Dutch laws and regulations in force
- unable to fill in a Dutch-language questionnaire or to answer the questions verbally.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Satisfaction with the AT device and the provision process (D-QUEST, KWAZO)

Secondary Outcome Measures

Name	Time	Method
Problems in daily life (IPPA), limitations in activities (DASH), quality of life (EQ-5D-5L)