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Exploratory Study About the Implementation of Technology in the Rehabilitation

NCT04833088 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 27

Last updated 2022-07-07

No results posted yet for this study

Summary

This qualitative study aims to identify the needs and recommendations of both patients and healthcare professionals in terms of rehabilitation technology, more specific three pre-defined user scenarios. These scenario were developed based on brainstorm sessions with healthcare professionals from the rehabilitation ward of UZ Brussel and AZ Sint-Maria Halle. The purpose of this study is to create an overview of recommendations that will be used to develop the smart devices in a later stage of the SAIRE project.

Conditions

  • Stroke
  • Parkinson Disease
  • Covid19
  • Neglect, Hemispatial

Interventions

OTHER

Focus group discussions

Focus group discussions will be organized to investigate the needs and requirements of the participants in terms of three pre-defined user scenarios.

Sponsors & Collaborators

  • Universitair Ziekenhuis Brussel

    collaborator OTHER

  • AZ Sint Maria Halle

    collaborator UNKNOWN

  • Odisee University college for applied sciences

    collaborator OTHER

  • Erasmus University Rotterdam

    collaborator OTHER

  • Jessa Hospital

    collaborator OTHER

  • Rehabilitation hospital Inkendaal

    collaborator UNKNOWN

  • Rehabilitation hopsital Revarte

    collaborator UNKNOWN

  • Vrije Universiteit Brussel

    lead OTHER

Principal Investigators

  • Eva Swinnen, Prof. Ph.D · Vrije Universiteit Brussel

Study Design

Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-06-10
Primary Completion
2022-04-01
Completion
2022-04-01

Countries

  • Belgium

Study Locations

More Related Trials

Entities

Diseases

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 NCT04833088 on ClinicalTrials.gov