- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01550874
STEP: Enhanced Physical Activity in Children and Youth With Epilepsy (STEP)
19. juni 2018 opdateret af: McMaster University
STEP: Enhanced Physical Activity in Children and Youth With Epilepsy: Developing Evidence of Impacts on Health, Functioning, Psychological Wellbeing, and Quality of Life
Epilepsy is common in childhood.
Children with epilepsy are at increased risk of impaired health, functioning, psychological well-being, and quality of life.
There is compelling evidence that physical activity improves the medical and psychosocial aspects of health in adults with epilepsy - but there are no such studies in children.
This study is to see if increased levels of physical activity can influence children's functioning, psychological well-being, and quality of life.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
There are many unfounded assumptions about the dangers of exercise in children with epilepsy - assumptions that may be seriously detrimental to children's health, and that we have good reason to challenge.
This project explores the innovative idea that enhancing physical activity in children with epilepsy will have a positive effect on medical and psychosocial outcomes.
The primary purpose of this study is to examine whether increasing physical activity levels through a six-month walking program, that includes behavioral counselling and self-monitoring of physical activity, as compared to varied un-standardized current practices, positively influences health and quality of life over one year.
The secondary purposes are to (i) determine which environmental and personal facilitators and barriers to physical activity are experienced when increasing physical activity levels through a six-month walking program; (ii) determine if physical activity levels established during the six-month program will be sustained over a subsequent six-month period that includes self-monitoring of physical activity only; (iii) identify aspects of health that are amendable to change with enhanced physical activity, and explore the relationships among physical activity and impairments, functioning, psychological well-being and quality of life; and (iv) assess if there is a dose-response relationship between physical activity and a variety of health and social factors and quality of life.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
122
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Ontario
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Hamilton, Ontario, Canada, L8S 4K1
- McMaster Children's Hospital
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Ottawa, Ontario, Canada, K1H 8L1
- Children's Hospital of Eastern Ontario
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
8 år til 14 år (Barn)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Has epilepsy, as confirmed by a pediatric neurologist, with at least 1 seizure in the previous 12 months
- Ambulatory
- Fluency English or French
- Intellectual functioning at or greater than grade 3 level, as judged by parents
- Access to a computer
Exclusion Criteria:
- Additional diagnoses of psychogenic seizures or autism
- Enrolled in a potentially confounding trial
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Andet
- Tildeling: Randomiseret
- Interventionel model: Enkelt gruppeopgave
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Ingen indgriben: Control Group
Wear the pedometer provided by study everyday with weekly charging and syncing of data.
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Eksperimentel: Experimental Group
Wear the pedometer provided by the study everyday and also participate in phone-based physical activity behavior-change counselling for 6 months and then check sustainability without further motivational support for another 6 months.
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Participants in the experimental group will be motivated by augmented behavior modification strategies aiming to increase performance by: (i) having access to the pedometer web page that allows them to view their automatically calculated goals, and (ii) get feedback about performance toward goals.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
CHEQOL-25
Tidsramme: Baseline, 16 week follow-up, 28 week follow-up
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Measure of quality of life
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Baseline, 16 week follow-up, 28 week follow-up
|
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KIDSCREEN-27
Tidsramme: Baseline, 16 week follow-up, 28 week follow-up
|
Will look at Psychological Well-Being (7items) subscale
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Baseline, 16 week follow-up, 28 week follow-up
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Step Count
Tidsramme: Baseline, 16 week follow-up, 28 week follow-up
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Will use step counts obtained from pedometer
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Baseline, 16 week follow-up, 28 week follow-up
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
KIDSCREEN-27
Tidsramme: Baseline, 16 week follow-up, 28 week follow-up
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Will look at Physical Well-Being (5 items), Parents and Autonomy (7 items), Social Support and Peers (4 items) and School Environment (4 items) subscales
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Baseline, 16 week follow-up, 28 week follow-up
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Gabriel M Ronen, MD, McMaster University
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
2. april 2012
Primær færdiggørelse (Faktiske)
31. marts 2018
Studieafslutning (Faktiske)
31. marts 2018
Datoer for studieregistrering
Først indsendt
8. marts 2012
Først indsendt, der opfyldte QC-kriterier
9. marts 2012
Først opslået (Skøn)
12. marts 2012
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
20. juni 2018
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
19. juni 2018
Sidst verificeret
1. juni 2018
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- REB 12-035
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
INGEN
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Epilepsi
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Boston Children's HospitalRekrutteringEpilepsi | Bevægelsesforstyrrelser | Dyskinesier | Ataksi | Neurologisk lidelse | Chorea | Myoklonus | Dyskinesi | Dystoni lidelse | Epilepsi hos børn | EDS | Bevægelsesforstyrrelser hos børn | Epilepsy-dyskinesi | Epilepsi-dyskinesi synkdomForenede Stater
Kliniske forsøg med Physical activity behavior-change counselling
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Wake Forest University Health SciencesNational Heart, Lung, and Blood Institute (NHLBI)AfsluttetFysisk aktivitetForenede Stater
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Massachusetts General HospitalNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)RekrutteringFysisk aktivitet | Insulin resistens | Pubertet | PCOS (polycystisk ovariesyndrom)Forenede Stater
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University of Vic - Central University of CataloniaIRIS-CC; AGAURAktiv, ikke rekrutterendePsykisk sundhedsproblemSpanien
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The Miriam HospitalUkendtSlag | Stillesiddende livsstil | Iskæmisk angreb, forbigående | Dyrke motionForenede Stater
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Centre Hospitalier Universitaire de Saint EtienneNational Cancer Institute, FranceAfsluttetKræft prostataFrankrig
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The University of Hong KongRekrutteringDemens | Plejerbyrde | Kognitiv svækkelse, mild | Demens, mildHong Kong
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Northeastern UniversitySociety for Pediatric Psychology; APA: American Psychological AssociationRekrutteringAutismespektrumforstyrrelse (ASD)Forenede Stater
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Cairo UniversityTilmelding efter invitation
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IVI BilbaoInstituto Valenciano de Infertilidad, IVI VALENCIAAfsluttet