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Completed

NCT Number: NCT02735460

Usability of Andago V2.0 in Gait Rehabilitation of Stroke Patients

Andago V2.0 is a recently developed overground gait and balance training device. Many patients in neurorehabilitation suffer from gait disorders, most typically after stroke. Since pharmacological therapies are basically not available, neurorehabilitation plays an important role in the treatment of such patients. The Andago V2.0 may represent a useful device in the rehabilitation of stroke and other neurological patients featuring a severe gait disorder. Therefore a study has been designed to investigate the usability of the Andago V2.0 in the setting of a neurorehabilitation clinic. The primary outcomes of this study are the usability and acceptance of the investigational medical device (IMD). Usability is mainly measured by the time spent for the set-up and release of the participant, achieved training times and distances, the number of stumbles, collisions and emergency stops and the error messages during the session. Besides patient and therapist satisfaction with the Andago V2.0 is recorded.

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Key information

Conditions

Brain Ischemia Brain Diseases Cardiovascular Diseases Central Nervous System Diseases Cerebrovascular Disorders Hemorrhage InTracranial Haemorrhage Intracranial Hemorrhages Nervous System Diseases Pathologic Processes Pathological Conditions, Signs and Symptoms Vascular Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Rehaklinik Zihlschlacht, Center for Neurological Rehabilitation

Zihlschlacht, Switzerland

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Informed consent as documented by signature
  • Primary diagnosis of cerebral infarction (ICD-10: I63.0-I63.9) or intracerebral haemorrhage (ICD-10: I61.0-I69.9) independent of its location, age or cause
  • Gait disorder defined by a category of 1 to 3 on the Functional Ambulation Classification (FAC) (17)
  • Age above 18 years
  • Admission to Rehaklinik Zihlschlacht for in-patient neurorehabilitation

Exclusion criteria

  • Inability of the participant to understand the informed consent or to follow the procedures of the study, e.g., due to language problems, psychiatric disorders, cognitive impairment or aphasia (item 9 of the National Institute of Health Stroke Scale (NIHSS) ≥2)
  • Weight >135 kg
  • Height >200 cm
  • Bone fragility (e.g., non-consolidated fractures or osteotomies including craniotomies, osteopenia, osteoporosis or symptoms or indices in the patient history that infer a higher risk of bone density reduction)
  • Unstable arthroplasty
  • Uncontrolled knee or ankle instability that would still pose a danger despite the Body Weight Support (BWS) (especially lateral instability)
  • Lack of head control
  • Joint contractures
  • Relevant differences in leg length
  • Skin lesions (including pressure sores or enteric stomata) in areas of contact with harness support or lower extremity loading (feet)
  • Relevant sensory impairment in the lower limbs and trunk, especially with reduced pain sensation
  • Recent history or significant risk of seizures
  • Relevant cardiovascular conditions, e.g., cardiac insufficiency and thoracotomy, uncontrolled orthostatic hypotension or other circulatory problems, vascular disorders of the lower limbs
  • Mechanical ventilation
  • Long-term infusions (e.g., baclofen pump, other intrathecal pumps)
  • Any medical condition preventing active rehabilitation and/or the use of the Andago V2.0 (e.g., respiratory disease, pregnancy, orthopedic conditions, infections or inflammatory disorders, osteomyelitis)
  • Participation in another interventional study within the 30 days preceding and during the present study

Treatment and study plan

Andago V2.0

Device

The Andago V2.0 is tested in 2 sessions, the first being a training session to define the probably optimal settings for the subsequent therapy session. In the therapy session the participant performs a specific parcours. Usually this parcours can be done within 10 minutes. However, the session is stopped as soon as the patient feels too exhausted or becomes too weary.

Primary outcomes

  1. Usability of the IMD according to the number of participants that are able to use the Andago V2.0

    Time frame: 3 weeks

  2. Acceptance of the IMD as measured by a therapist satisfaction questionnaire

    Time frame: 3 weeks

  3. Acceptance of the IMD as measured by a patient satisfaction questionnaire

    Time frame: 3 weeks

Sponsors and collaborators

Lead sponsor

Rehaklinik Zihlschlacht AG

Other

Registry information

Official study title

Single-center Usability Study of the Overground Gait and Balance Training Device Andago V2.0 in Patients With Gait Disorder After Stroke at a Center for Neurological Rehabilitation

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Apr 12, 2016
Registry last updated
Oct 1, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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