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Implementation of a gait center training to improve walking ability and vital parameters in inpatient neurological rehabilitation. A cohort study.

Implementation of a gait center training to improve walking ability and vital parameters in inpatient neurological rehabilitation. A cohort study.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00014090
Enrollment
500
Registered
2018-03-06
Start date
2015-07-02
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

neurological disorders

Interventions

Group 1: G-EO System Gait trainer therapy, 5 days / week, add-on therapy to the standard rehabilitation program during the entire rehabilitation process

Sponsors

Klinik Bavaria Bad Kissingen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients of neurological inpatient rehabilitation

Exclusion criteria

Exclusion criteria: Exclusion criteria for the persons were: 1) no training because of deterioration of the general condition, a referral to an primary care clinic, isolation due to multiresistant germs and impossible mobilization in the wheelchair and 2) Contraindications to treatment with gait trainers such as implantation of a cardiac pacemaker, artificial joint replacement in hip joints in general and knee joints up to two years after implantation, osteoporosis, manifested leg length difference or scoliosis or psychotic illnesses excluded the treatment. The maximum weight limit of the subjects was 150 kilograms.

Design outcomes

Primary

MeasureTime frame
As a primary outcome the development of walking ability was examined using the Functional Ambulation Categories. The measured values ??served to form the rehabilitation coefficient. Assessment testing of walking ability took place at the beginning and end of rehabilitation.

Secondary

MeasureTime frame
Secondary outcome measures included expiratory vital capacity and systolic and diastolic blood pressure. The vital capacity was determined by means of pocket spirometer and the blood pressure by means of blood pressure cuff and stethoscope. The cardiopulmonary vital signs were tested at the beginning and at the end of the rehabilitation.

Countries

Germany

Contacts

Public ContactStephanie Reichl

Klinik Bavaria Bad Kissingen

reichl.s@klinik-bavaria.com0971 8292501

Outcome results

None listed

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