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Participation-related attainment through therapies and assistive devices in patients with mobility-restricting paralytic syndromes

Participation-related attainment through therapies and assistive devices in patients with mobility-restricting paralytic syndromes - NeuroMoves

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00020487
Enrollment
250
Registered
2020-02-18
Start date
2020-05-12
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

Paraplegia, Hemiplegia, Parkinson disease

Interventions

Group 1: Assessments are conducted at three visit points (baseline, interim and final visits) within the 8-month observation period. The baseline visit takes place in the clinic at the end of the init

Sponsors

Universitätsklinikum Heidelberg Klinik für Paraplegiologie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1) Patients with paraplegia, stroke or Parkinson disease at the end of inpatient rehabilitation 2) Age between 18-85 3) Limitation of walking ability/mobility (Score = 4 at item 8 of mRMI) 4) At least mobile, at study start, with wheelchair (also an electric wheelchair) 5) Able to understand and follow the study procedures (use of tablet, WLAN access at least once a week guaranteed) 6) Patient is able to consent 7) Signed informed consent form

Exclusion criteria

Exclusion criteria: 1) Severe psychiatric diseases (e.g. Schizophrenia, ongoing suicidal tendencies) 2) Depending on a respirator 3) For repeated stroke pre-existing limitation of the ability to walk/mobility 4) No capability to move independently at study start (bedridden: mRS = 5) 5) All physical and mental limitations which prevent the implementation of the study procedure significantly 6) Severe cognitive deficits (where applicable: minimental state examination = 23, e.g. 3x lack of orientation)

Design outcomes

Primary

MeasureTime frame
1) Structural recording of the quality of therapy and wheelchair supply and care results depending on patient factors, especially with regard to participation orientation 2) Objective measurement of mobility parameters (walking distance and/ or wheelchair distance) in daily life by using activity tracking.

Secondary

MeasureTime frame
1) Recording of mobility-related therapies and assistive devices 2) The individual supply network of patients with a focus on the ambulatory physiotherapy 3) Identification of effective therapy and assistive devices 4) Identification of the need for coordination of measures

Countries

Germany

Contacts

Public ContactTamara Spingler

Universitätsklinikum Heidelberg Klinik für Paraplegiologie

tamara.spingler@med.uni-heidelberg.de06221 56 39997

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 23, 2026