Retrospective analysis of patients’ records using the certified and approved Innowalk® to evaluate indication, usage, medical benefit and safety

• Conditions: G80; G73; G12; Cerebral palsy; Disorders of myoneural junction and muscle in diseases classified elsewhere; Spinal muscular atrophy and related syndromes

• Registration Number: DRKS00014980
• Lead Sponsor: Made for Movement GmbH

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2018-07-19
• Study Completion: 2019-02-01
• Results First Posted: 2022-02-23
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

1. Active use of the Innowalk® device at the time of data analysis
2. Signed informed consent forms after patient /care-giver information
3. patients from the period 09/2014 to 08/2017 are evaluated

Exclusion Criteria

1. Inability of patient/caregiver to understand the nature and purpose of this retrospective analysis
2. Information by patient/caregiver that the Innowalk® has not been used at all
3. Missing key variables (age / gender / indication / date of documentation) and/or poor quality of data (more than 20% of data missing or illegible) on questionnaire

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The aim of this analysis is to learn more about the prescription patterns, indications, desirable goals and clinical results of dynamic standing with the Innowalk® in patients with severe physical disabilities in daily clinical practice.<br>