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Treatment studiy with locomotor training vs conventional physiotherapy in patients with pusher behvaviour

Treatment studiy with locomotor training vs conventional physiotherapy in patients with pusher behvaviour - IFB Project2

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00003444
Enrollment
30
Registered
2013-11-28
Start date
2011-12-09
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

R29.5 R29.3 R27 I69.3

Interventions

Group 1: 15 patients receive conventional physiotherapy (8 to 10 hours over 2 weeks). Measurement points: before and immediate after the intervention phase, 2 weeks after the end of the intervention p

Sponsors

Klinikum der Universität München, Campus Großhadern
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: - Patients after hemispheric ischemic or heamorrhage stroke - Age 18 to 90 years - Right or left hemiparesis - Patients are classified with pusher behaviour according to the SCP (cut-off > 0 per component) - 30 min in a vertical body position ('standing')

Exclusion criteria

Exclusion criteria: Exclusion criteria for the therapy with the Lokomat: - orthostatic hypotension - bone fractures - sever osteoporosis - Problems with the skin at the lower extremities (because of the cuffs) - known orthopaedic disorder (e.g. arthrosis) - significant asymmetries (e.g. length of legs) - body height 190 cm or body weight >150 kg Exclusion criteria for the Spacecurl (SPV): - severe cardiovascular disease - known thrombosis - known aneurism - instable spine - neurosis/ psychosis - pregnancy - body height 195 cm or body weigth >130 kg

Design outcomes

Primary

MeasureTime frame
Immediately before and after the intervention phase, two weeks after the end of the intervention and at discharge of the patient 2 clinical scales to assess pusher behaviour will be conducted: - Scale for Contraversive Pushing (SCP) - Burke Lateropulsion Scale (BLS)

Secondary

MeasureTime frame
The following outcome measures will be assessed immediately before and after the intervention phase, two weeks after the intervention phase and at discharge of the patient: - head, trunk and leg orientation documented by photographs - subjective visual vertical (using the bucket test) - subjective postural vertical (using the Spacecurl) - Performance Oriented Mobility Assessment (POMA) - Walking ability (FAC)

Countries

Germany

Contacts

Public ContactJeannine Bergmann

Schoen Klinik Bad Aibling

jbergmann@schoen-kliniken.de+49 (0) 8061-903-0

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 5, 2026