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ERTUN STUDY

The Effectiveness of Rehabilitation Treatment Using the 'Nigirukun' Glove for Patients with Hand Function Disorders

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs052250112
Enrollment
44
Registered
2025-09-17
Start date
2026-02-25
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

Hand dysfunction

Interventions

Participants are allocated to two groups: the "Nigirukun(R)" group, who wear the "Nigirukun(R)" glove, and the non-use group, who do not wear any device. Each group performs finger grip exercises twic

Sponsors

Kobayashi Yasuyo
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients who are currently hospitalized at Nara Medical University Hospital for rehabilitation of decreased physical function 2) Patients with disability of hand and finger (physical disability certificate level 7, 4, or 3 as a guideline) 3) Patients who cannot undergo finger function rehabilitation using conventional training equipment 4) Patients aged 18 years or older 5) Patients who have given written consent (In cases where the patient is unable to sign due to hand dysfunction, etc., it is acceptable for a witness to sign and date the consent form on behalf of the patient

Exclusion criteria

Exclusion criteria: 1) Patients with joint deformities or amputated fingers above the wrist 2) Patients diagnosed with dementia 3) Patients with fragile skin who may suffer skin damage from wearing gloves 4) Patients who cannot be assessed for hand function 5) Patients undergoing acute treatment for central nervous system disorders and neuromuscular disorders ( e.g.,Guillain-Barre syndrome,myositis) 6) Patients with severe contracture or spasticity 7) Patients with severe peripheral arterial disease, congestive heart failure or phlegmasia cerulea dolens 8) Patients with suppurative phlebitis 9) Patients whom the physician deems unsuitable for treatment

Design outcomes

Primary

MeasureTime frame
Change in fingertip pinch strength from enrollment to 2 weeks after starting protocol treatment

Secondary

MeasureTime frame
Changes in fingertip pinch stength over time Changes in lateral finger pinch strength and three-finger pinch strength over time Changes in five-finger crush strength over time Changes in forearm circumference over time Changes in Purdue Pegboard Test (manual dexterity test) over time Changes in Quick DASH over time Changes in Functional Independence Measure(FIM) over time

Contacts

Public ContactTetsurou Kitamura

Nara Medical University Hospital

rehaka@naramed-u.ac.jp+81-744-22-3051

Outcome results

None listed

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