Ireland
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Recruiting Observational

The Effects of a Dynamic Arm Support in Daily Life

NCT07121075 · tracked via the Priya Life Science Netherlands tracker
Phase
Observational
Started
2024-12-02
Last updated
2025-08-13

Condition(s) studied

Neuromuscular DiseaseNeuromuscular DisabilityAssistive TechnologyActivities of Daily LivingOccupational TherapyUpper Limb

Investigational drug(s) / intervention(s)

Dynamic arm support

Dynamic arm support: The participant will receive a new dynamic arm support.

Study summary

The goal of this mixed method study is to learn about how a dynamic arm support device (DAS) helps people with everyday activities. The study focuses on people with neuro(-muscular) conditions, age 16 and older. The research questions that are formulated, are:

* How does a person experience their daily activities, with and without a DAS?
* What are the contextual (external and personal) factors that influence the use of a DAS?

Participants will take part in three testing sessions. In each session, they must complete a few questionnaires and participate in an interview. The first time, without DAS. In the second and third session, they will be using their DAS (resp. 3 to 4 weeks and 3 months). The data collection will be executed by phone, digital questionnaires and/or paper.

Eligibility

Sex
ALL
Min age
16 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age: 16 and oler * Being able to understand and comprehend test instructions * Using a DAS from Focal Meditech (Balancer, Flowing, Dowing, Gowing 2 or Top Help) Exclusion Criteria: /

Primary outcome measure(s)

  • Canadian Occupational Performance Measure (COPM) — Test moment 0: Assessment before delivery of dynamic arm support (DAS), Test moment 1: assessment 3 weeks after delivery, Test moment 2: assessment 3 months after delivery
    The COPM is a semi-structured interview, where the participants give at least 5 activities of daily life. They give a score of satisfaction and performance (between 1 and 10) on these 5 activities.
  • Psychosocial impact of assistive devices scale (PIADS) — Test moment 1: assessment 3 weeks after delivery, Test moment 2: assessment 3 months after delivery
    The psychosocial impact of assistive devices scale is a 26-item, self-report questionnaire designed to assess the effects of an assistive device (the DAS) on functional independence, well-being, and quality of life. Scores on competence (between -3 and +3), adaptability (between -3 and +3) and self-esteem (between -3 and +3).

Trial sites (1)

FacilityCityRegionStatus
Focal Meditech BV (their clients in their home situation) Tilburg Netherlands Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07121075 on ClinicalTrials.gov ↗ ← All trials in the Netherlands