- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04707755
Motor Imagery Technique on Lower Limb Function Among Stroke Patients.
Effects of Motor Imagery Technique on Lower Limb Function Among Stroke Patients.
To determine the effects of motor imagery technique on lower limb function among stroke patient.
To determine the effects of motor imagery technique on lower limb spasticity among stroke patients.
To determine the effects of motor imagery technique on gait among stroke patients.
To determine the effects of motor imagery technique on quality of life among stroke patients
Studieoversigt
Status
Intervention / Behandling
Detaljeret beskrivelse
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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-
KPK
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Peshawar, KPK, Pakistan, 251900
- Bibi Zahida Memorial Teaching Hospital
-
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Adult without ADHD by Adult ADHD Self-Report Scale score.
- History of no more than one stroke.
- Lower limb muscles spasticity with the grade 1+ or 2 on modified Ashworth in scale.
- Mini-mental status score more than 25.
- Patients who are less than 6 months post-stroke.
- Modified Rankin scale score is 4.
Exclusion Criteria:
- Lesion of frontal, parietal and basal ganglia
- Excessive spasticity that is score of>3 on modified Ashworth spasticity scale.
- Any musculoskeletal disorder impeding lower limb function.
- Participating in any experimental rehabilitation or drug studies.
- Bed ridden patient.
- Subjects psychiatric disorder or dementia.
- Any neglect of space on the affected side, or any other neurological disease or auditory or visual.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Motor imagery technique
Motor Imagery technique Plus Conventional Physical therapy
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The patient will sit on chair in a quiet room. The patients will be observing motor performance in video, motor performance video will consist of (1) knee flexion and extension movement, (2) sitting to standing movement, (3) stepping movement, (4) walking, (5) climbing and descending stairs. Addition to motor imagery, the patients will be provided the passive stretching, ROM exercises, sitting to standing, anteroposterior step, climbing and descending stairs. |
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Aktiv komparator: Conventional Physical therapy
passive stretching, ROM exercises, sitting to standing, anteroposterior step, climbing and descending stairs.
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It includes passive stretching, ROM exercises, sitting to standing, anteroposterior step, climbing and descending stairs.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Lower Extremity Function scale
Tidsramme: 8 weeks
|
It is 20 items questionnaire, measure the lower extremity function scoring from 1 to 4 for each items, in which minimum score is 0 and maximum score of 80 shows the maximum functional status.
It has a valid and reliable tool to measure the lower extremity functional status.
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8 weeks
|
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Dynamic Gait Index
Tidsramme: 8 weeks
|
It assess gait, balance and fall risk, with 24 is the maximum score, in which 19 or less have been related to increase incidence of falls.
It has high reliability and validity in the stroke population.
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8 weeks
|
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Time Up and Go test
Tidsramme: 8 weeks
|
It assess a person's mobility and requires both static and dynamic balance.
Score of less than 10 seconds indicate freely mobile,<20 seconds mostly independent, 20-29 seconds variable mobility, >30 seconds Impaired mobility.
It is reliable, valid, and easy to administer clinical tool in stroke patients.
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8 weeks
|
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Stroke Specific Quality of Life Scale
Tidsramme: 8 Weeks
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It is a self-report questionnaire, measure the quality of life in stroke patients consisting of 49 items in the 12 domains.
Scoring from 1 to 5 , in which 1 shows strongly agreement and 5 shows strongly disagreement.
It is a reliable and valid tool for measuring the quality of life for stroke patients.
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8 Weeks
|
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Modified Ashworth scale
Tidsramme: 8 Weeks
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It measures the spasticity, ranging from 0 means normal tone to 4 shows increased tone to such extent where passive movement is not possible.
It has good intra-rater reliability and validity in stroke patients .
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8 Weeks
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Mirza Obaid Baig, MSPT(NMR), Riphah International University
Publikationer og nyttige links
Generelle publikationer
- Pedersen SG, Heiberg GA, Nielsen JF, Friborg O, Stabel HH, Anke A, Arntzen C. Validity, reliability and Norwegian adaptation of the Stroke-Specific Quality of Life (SS-QOL) scale. SAGE Open Med. 2018 Jan 8;6:2050312117752031. doi: 10.1177/2050312117752031. eCollection 2018.
- Gul I, Malik MS, Halim A, Rauf S. POST STROKE DEPRESSION: EXPERIENCE AT A TERTIARY CARE HOSPITAL OF PAKISTAN. Pakistan Armed Forces Medical Journal. 2019 Aug 27;69(4):779-83.
- Paravlic AH, Pisot R, Marusic U. Specific and general adaptations following motor imagery practice focused on muscle strength in total knee arthroplasty rehabilitation: A randomized controlled trial. PLoS One. 2019 Aug 14;14(8):e0221089. doi: 10.1371/journal.pone.0221089. eCollection 2019.
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- REC00664 Izharuddin
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
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