- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04835740
Effects of High-intensity Interval Aerobic Training on Balance, Walking Capacity, and Quality of Life in Patients With Sub-acute Stroke
Hemiplegia is one of the most common sequelae of stroke. Stroke is the leading cause of disability in adults all around the world. Stroke survivors can suffer several neurological impairments and deficits which have an important impact on patient's quality of life and which increase the costs for health and social services. After stroke, impairments in ADLs and functional status, deterioration in health related quality of life can be seen.
The purpose of this study is to Determine the effect of Aerobic exercise training on Balance, Walking capacity and quality of life in sub-acute stroke.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Lahore, Pakistan
- Akhtar Saeed 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:
- 18 to 75 years of age.
- Ischemic Stroke that occurred in the recent 3 months.
- Who can walk independently or by using assistive device.
- Have a minimum Chedoke McMaster Stroke Assessment (CMSA) leg impairment score of 3 but less than 7.
Exclusion Criteria:
- Patients were excluded from the study if they have a stroke that occurs more than 3 months.
- Hemorrhagic Stroke.
- If resting blood pressure more than 160/100 even after taking medications
- Have by-pass surgery in recent 3 months.
- Other musculoskeletal problems which restrict the patient's ability to do aerobic activity.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Aktiv komparator: Conventional Rehabilitation
Based on the functional capacity of each participant, customized Aerobic exercise plan was designed by the on-site physiotherapist.
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All the participants underwent 5 weeks of High intensity interval training.
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Eksperimentel: Combined Training (conventional rehabilitation plus high-intensity interval training):
The patients received 40 minutes of High intensity interval treadmill training in addition to their normal conventional rehabilitation.
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All the participants underwent 5 weeks of High intensity interval training.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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6 Minute walk Test
Tidsramme: 5 weeks
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To determine the cardiorespiratory fitness of individual after sub-acute stroke.
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5 weeks
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Berg Balance test and rating scale
Tidsramme: 5 weeks
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The scale is used to determine the Balance and stability of patient.
Total score of the scale is 56.
A score of < 45 indicates individuals may be at greater risk of falling.
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5 weeks
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Stroke Impact scale
Tidsramme: 5 weeks
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The scale is used to measure the impairment and quality of life after stroke.
The scale consists of 8 domains.
In this study, only 4 domains related to hand function ,strength, mobility and Activity of daily living were used.The maximum score is 140.
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5 weeks
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Samarbejdspartnere og efterforskere
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
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- IRB/ASCRH/0006/2020
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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