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Multi-center observational study and present status survey for the establishment of the standard method for the long-term use of HAL.

Multi-center observational study and present status survey for the establishment of the standard method for the long-term use of HAL. - NCY extended03

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1092220433
Enrollment
200
Registered
2019-08-02
Start date
2019-08-12
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

SMA, SBMA,ALS,CMT, distal myopathy, inclusion body myositis (IBM), congenital myopathy, muscular dystrophy and other diseases including hereditary spastic paraplegia and HAM, and SMON.

Interventions

Intervention type: Name of intervention: Dose form / Japanese Medical Device Nomenclature: Route of administration / Site of application: Dose per administration: Dosing frequency / Frequency of use:

Sponsors

None
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients for whom at least one course of treatment using HAL was performed, and the conditions before and after the course were evaluated, or such a course and evaluation are planned (2) Patients who can opt out using consent written by themselves or using a prescribed method.Patients who can provide his/her own written consent. For patients aged 16 or older and under 20, informed consent by legal guardian is required in addition to him/her consent. For patients under 16, obtaining informed assent by him/her is encouraged after explaining the study in readily comprehensible language. If the patient has sufficient ability to consent but has difficulty writing due to primary disease progression, written consent is to be obtained from the patient's legally acceptable representative after confirming that the subject himself/herself consents to participate in the study;

Exclusion criteria

Exclusion criteria: (1)In the case that patient's length and shape are not fit to "HAL(Lower Limb Type)". (2)In the case that patient is not allowed to stand and/or walk with "HAL(Lower Limb Type)". (3)In the case that electrodes are not allowed to be put on the patient's skin because of the patient's skin disease. (4)Ineligibility for participating in this study according to the investigator or subinvestigator. The above (1)-(3) correspond to contraindications/prohibitions for HAL for medical use (lower limb-type).

Design outcomes

Primary

MeasureTime frame
Status of cybernetic walk treatment using HAL 2-min walk test;the distance (m) walked at the fastest speed for 2 minutes

Secondary

MeasureTime frame
10-m walk test (speed);the maximum walk speed (m/s), mean stride length (m/sep), and cadence (step/sec) Manual muscle test (MMT);hip flexion and extension, knee flexion and extension, and right and left ankle dorsiflexion, and plantar flexion Barthel index Japanese version of the DRS Body weight Blood creatine kinase level

Countries

Japan

Contacts

Public ContactTakashi Nakajima

National Hospital Organization Niigata National Hospital

225-kenkyuu@mail.hosp.go.jp+81-257-22-2126

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026