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A Pilot Study of Neuro Hand Orthosis Program In Stroke Upper Limb Rehabilitation

A Pilot Study of Neuro Hand Orthosis Program: A Promising Restorative Therapy Treatment for the Severe Paralytic Arm in Subacute Stroke Rehabilitation

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00646347
Acronym
NHOP
Enrollment
30
Registered
2008-03-28
Start date
2008-03-31
Completion date
2010-07-31
Last updated
2009-02-05

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

Conditions

Paralytic Stroke

Keywords

stroke, upper limb rehabilitation, treatment, movement recovery from sever paralytic upper limb, neuro hand orthosis, self practice program, subacute

Brief summary

The implementation of Neuro Hand Orthosis Upper Limb Program can significantly improve the severe stroke paralytic arm in subacute rehabilitation as compared with the use of conventional therapy.

Detailed description

The neuro hand orthosis is based on a design of dynamic hand orthosis for orthopaedic patients. We attempt to apply such an orthosis on stroke patients to aid in regaining movement from severe paralytic arm by helping the patients to support their wrist and finger in a functional position for grasping. The patient is then encouraged to produce voluntary movement from the severe paralytic arm to transport an object (ball) from place to place either in sitting or standing position. Since intensive arm usage is associated with neuro reorganisation, we propose designing a program with the neuro hand to encourage usage of the paralysed hand and help overcome the barriers of poor motivation and lack of arm usage through self practice program.

Interventions

OTHERConventional upper limb stroke rehabilitation

Patient will be given a ten weeks conventional upper limb therapy. 3 sessions will be provided weekly in the first 4 weeks and 2 therapy sessions will be provided weekly in the subsequent 6 weeks. Patients will receive half an hour of conventional therapy in each session. Patient will be taught to carry out two and half hours conventional self practice exercise daily for a period of ten weeks.

DEVICENeuro Hand Orthosis Program (NHOP)

The NHO is based on a design of dynamic hand orthosis for orthopaedic patients after hand surgery. We use it to support CVA patient's wrist and finger to perform grasping to transport an object (ball) from place to place to achieve the follows; 1. NHO can assist stroke patients to experience successful hand grasping with an object and produce voluntary movement from their paralytic arm. This successful experience will positively reinforce the patient to continue to use their paralytic arm and change the patient's behavior and perception in the arm usage. 2. The NHO Program is able to engage patients to perform their exercises and activities by themselves independently with the effect of intensive therapy. The intervention (NHOP) group will receive same treatment intensity as the control group but with a Neuro Hand Orthosis.

Sponsors

National Council Of Social Service, Singapore
CollaboratorOTHER
St Luke's Hospital, Singapore
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
50 Years to 89 Years
Healthy volunteers
No

Inclusion criteria

* Post stroke between one week to three months and medically stable * Right Hemiplegia with right hand dominant * Able to stand with minimum assistance * AMT score not lesser then 7/10 * Motricity Index Arm Score \<36/100

Exclusion criteria

* Unable to commit to the Neuro Hand Orthosis Program (either as in or out patients) for 10 weeks according to the program regime or unable to follow the control group regime for 10 weeks * Pre-existence shoulder or upper limb pain * Pre-existence moderate or severe hand oedema * Patients with terminal disease * Resident of Institution (eg, Nursing home etc prior to admission) * Pre-existing upper limb disability on affected arm * Psychiatric problem

Design outcomes

Primary

MeasureTime frame
Action Research Arm Test (ARAT)week 4 , week 10 , 6 months and 12 months
Motricity Indexweek 4 , week 10 , 6 months and 12 months

Secondary

MeasureTime frame
Motor Activity Log (MAL)At admission, week 4 , week 10 , 6 months and 12 months
Modified Ashworth Scale for grading SpasticityAt admission, week 4 , week 10 , 6 months and 12 months
Shoulder pain at admissionAt admission, week 4 , week 10 , 6 months and 12 months

Countries

Singapore

Contacts

Primary ContactGribson Yu Chun Chan, Master
gribsonchan@slh.org.sg65632281

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026