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- Klinische proef NCT01886183
Effects of Training in a Virtual Environment in Chronic Stroke Patients
1 november 2018 bijgewerkt door: University of Sao Paulo General Hospital
Effects of Training in a Virtual Environment on the Motor Function,Postural Control and Quality of Life in Chronic Stroke Patients: A Randomized Controlled Trial
The objective of this work will be compare the effects of two balance training programs, one Nintendo Wii Fit-based and the other traditionally-based without the use of a gaming system, on the (1) motor function, (2) cognition, (3) balance and (4) gait in chronic stroke patients.
It is a prospective, single blinded, randomized clinical trial performed at Center of Research of the courses of Speech Therapy, Physical Therapy and Occupational Therapy of São Paulo University.
Forty patients will be randomly assigned in control and experimental group, 20 each one.
Studie Overzicht
Toestand
Voltooid
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
The objective of this work is to compare the effects of two balance training programs, one Nintendo Wii Fit-based and the other traditionally-based without the use of a gaming system, motor function, balance and quality of life in chronic stroke patients.
It is a prospective, single-blinded, randomized clinical trial performed at Center of Research of the courses of Speech Therapy, Physical Therapy and Occupational Therapy of São Paulo University.
Forty chronic stroke patients are randomly in control and experimental group, 20 each one.
Both groups conduct 14 training sessions, twice a week, for seven weeks.
Each session will consist a 30 minute-global-exercise series including stretching, muscle strength and axial mobility exercises.
After this, both groups will performed more 30 minutes of balance training: the control group will performed balance exercises without external cues, visual or auditory feedbacks or cognitive stimulations; the experimental group will performed the balance training with 8 Wii Fit games which stimulate motor and cognitive functions.
The main outcome measures will be: (1) the lower limb subscale of the Fugl-Meyer Assessment (FMA-LE); (2); Balance Evaluation Systems Test (BESTest);(3) the Stroke-Specific Quality of Life (SS-QOL); (4) 6- minute walk test (6MWT) and (5) The limits of stability (LOS).
Studietype
Ingrijpend
Inschrijving (Werkelijk)
40
Fase
- Niet toepasbaar
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
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São Paulo, Brazilië, 05360-160
- Department of Physiotherapy, Communication Science & Disorders, Occupational Therapy, School of Medicine, University of São Paulo
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
18 jaar tot 65 jaar (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
Inclusion Criteria:
- hemiparetic status resulting from a single stroke at least 6 months earlier;
- the ability to walk 10 m independently with or without an assistive device;
- the absence of a musculoskeletal condition that could potentially affect the ability to walk safely;
- the absence of serious visual impairment or a hearing disorder;
- power of at least grade 3 in the hemiplegic lower extremity;
- able to understand and follow simple instructions.
Exclusion Criteria:
- a Montreal Cognitive Assessment (MoCA) score of < 20;
- severe dementia or aphasia;
- hemispatial neglect, ataxia or any other cerebellar symptom;
- inability to stand without minimal assist;
- Impaired vision
- Uncontrollable medical complications
- participation in other studies or rehabilitation programs
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: Virtual Reality Training
The virtual reality training will be done by experimental group with ten games of Nintendo Wii Fit.
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The participants of the study will be trained 8 balance games during 14 sessions
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Actieve vergelijker: Control group: Physical Therapy
The Control Group will be trained by conventional Physical Therapy exercises.
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Patients of the control group will be trained with balance exercises.
Andere namen:
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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The lower limb subscale of the Fugl-Meyer Assessment (FMA-LE)
Tijdsspanne: up to 2 months
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FMA-LE is a subscale measuring lower limb motor recovery.
It examines movement and coordination of the hip, knee, and ankle in the supine, sitting, and standing positions.
Each item is scored on a 3-point scale (0, cannot perform; 1, partially performs; 2, performs fully).
The score range is 0 to 34, with higher scores indicating better lower limb motor performance
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up to 2 months
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Balance Evaluation Systems Test (BESTest)
Tijdsspanne: Up 2 months
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Balance Evaluation Systems Test (BESTest) measures balance.
It includes 36 items that evaluate performance of 6 balance systems: biomechanical constraints, stability limits/verticality, anticipatory postural adjustments, postural responses, sensory orientation, and stability in gait.
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Up 2 months
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6-minute walk test
Tijdsspanne: Up to 2 months
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The 6MWT is a practical simple test.
This test measures the distance that a patient can quickly walk on a flat, hard surface in a period of 6 minutes (the 6MWD).
The 6MWT has been used as a measure of functional status of patients.
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Up to 2 months
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Stroke specific quality of life scale
Tijdsspanne: Up to 2 months
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Stroke Specific Quality of Life Scale is a self-report assessment that includes 12 stroke specific subscales with 49 items.
The Stroke Specific Quality of Life Scale attempts to capture the domains of stroke specific QOL that are insufficiently assessed with generic QOL measures.
The 12 subscales, which are unidimensional, are Energy, Family Role, Language, Mobility, Mood, Personality, Self-Care, Social Roles, Thinking, Upper Extremity Function, Vision, and Work-Productivity.
Participants responded to each item on a 5-point scale.
Domain scores are the averages of the item scores, and the total score is the average of the domain scores.
All summary scores therefore range from 1 to 5. Higher scores indicate better function.
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Up to 2 months
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Limits of Stability
Tijdsspanne: Up to 2 months
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The Limits of Stability subtest quantifies the maximum distance a person can intentionally displace their center of pressure (COP) from start position of midline COP centered over the base of support to eight targets.
Location and movement of the COP was indicated by a cursor display projected on a screen in front of the subject.
As targets were highlighted, the subject was to move the COP cursor quickly and accurately as possible towards a target located on the Limits of Stability perimeter and hold position as close to the target as possible.
The parameters include COP movement velocity and directional control (% to target).
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Up to 2 months
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Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Onderzoekers
- Hoofdonderzoeker: Tatiana P Oliveira, PhD student, University of Sao Paulo
- Hoofdonderzoeker: Camila S Miranda, Ms Student, University of Sao Paulo
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
1 februari 2014
Primaire voltooiing (Werkelijk)
1 juni 2017
Studie voltooiing (Werkelijk)
1 februari 2018
Studieregistratiedata
Eerst ingediend
20 juni 2013
Eerst ingediend dat voldeed aan de QC-criteria
20 juni 2013
Eerst geplaatst (Schatting)
25 juni 2013
Updates van studierecords
Laatste update geplaatst (Werkelijk)
2 november 2018
Laatste update ingediend die voldeed aan QC-criteria
1 november 2018
Laatst geverifieerd
1 juli 2018
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- USPNEC005
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .
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