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Implementation of a technology-assisted programme to intensify upper limb rehabilitation in neurologically impaired participants: A prospective study.

Identifieur interne : 001814 ( Main/Exploration ); précédent : 001813; suivant : 001815

Implementation of a technology-assisted programme to intensify upper limb rehabilitation in neurologically impaired participants: A prospective study.

Auteurs : Mary P. Galea [Australie] ; Fary Khan ; Bhasker Amatya ; Alaeldin Elmalik ; Marlena Klaic ; Geoff Abbott

Source :

RBID : pubmed:27068229

Descripteurs français

English descriptors

Abstract

OBJECTIVE

To evaluate the implementation of a technology-assisted programme to intensify upper limb rehabilitation after stroke and other neurological conditions in an Australian community cohort.

METHODS

A "Hand Hub" was established in a tertiary hospital. Intervention was delivered via individual or group sessions for a period of up to 6 weeks, in addition to the patients' regular therapy. Patients were assessed before and after the programme using validated measures.

RESULTS

A total of 92 participants completed both assessments (mean age 57 years (standard deviation 17 years), 58% male and 88% with stroke). Post-intervention, participants showed significant improvement in arm function and strength (p < 0.001, effect sizes (r) = 0.5-0.7), streamlined Wolf Motor Function Test score (p < 0.05, r = 0.2-0.4), improved muscle tone on the Modified Ashworth Scale (p < 0.001, r = 0.4), Functional Independence Measure (locomotion, mobility and psychosocial subscales (p < 0.05, r = 0.2-0.3). Quality of life (EQ-5D) and overall health also improved significantly (p < 0.01 for all, r = 0.3-0.6).

CONCLUSION

The "Hand Hub" programme is feasible and showed promising results for upper limb function in persons with neurological disorders. The findings need to be further confirmed in a larger study sample, with a longer follow-up.


DOI: 10.2340/16501977-2087
PubMed: 27068229


Affiliations:


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<b>OBJECTIVE</b>
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<p>A "Hand Hub" was established in a tertiary hospital. Intervention was delivered via individual or group sessions for a period of up to 6 weeks, in addition to the patients' regular therapy. Patients were assessed before and after the programme using validated measures.</p>
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