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

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00014980

Enrollment

Registered

2018-07-19

Start date

2018-07-11

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

G80 G73 G12

Interventions

Group 1: The analysis will enable insight into indications, age and gender distribution, disability levels, mental/sensoric and vital functions, motoric functions and mobility skills, intestinal funct

Eligibility

Sex/Gender

All

Inclusion criteria

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

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

Design outcomes

Primary

Measure	Time frame
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.	—

Countries

Germany

Contacts

Public ContactJens Kleine

Made for Movement GmbH

info.de@madeformovement.com+49(0)511-2348160

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026