- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT01785498
Healthy Lifestyles for Children With Complex Heart Problems (ReACH)
Healthy Lifestyles for Children with Complex Heart Problems is a planning and resource development project. The goal of the project is to develop an implementation plan that would enable children with complex heart problems to lead healthy, active lives within their own community. The primary goal of the project is to promote physical activity, because the physical and mental health benefits of activity are very important for these children. Children with complex heart problems have a higher risk for obesity, diabetes, acquired heart disease and mental health problems than their healthy peers. The physical health benefits of physical activity are well known, but physical activity is also key for children's mental health. Physical activity enables children to socialize with peers and create bonds and friendships. Physical activity participation also directly elevates mood through the release of brain chemicals. Children with complex heart problems are also known to experience fear and anxiety related to physical activity. This project will also develop strategies to promote healthy eating and the prevention of physical activity-related injuries to these children and their families. Children with complex heart problems are at higher risk of overweight and obesity and face unique injury risks related to pacemakers or their medications.
Extensive consultations with families and caregivers have identified needed supports for physical activity lifestyles, mental health, healthy eating and injury prevention for these children. The goal of the interviews was to understand the positive and negative influences on physical activity and healthy lifestyles for these children. Analyses of the interview content was used to develop a detailed, step-by-step implementation plan to provide the supports necessary for children with complex heart problems to lead active, healthy lives in their own community, with their family and friends. The implementation plan specifies changes to family education and counselling resources, clinical care routines, and communication among professionals and families.
The clinical trial will evaluate the impact of implementing the family supports and changes to practice previously developed. Surveys will be completed by families attending the cardiac clinic before and after the changes to practice and additional resources are made available. Interviews will be utilized to gather additional feedback from professionals and families that receive counselling utilizing the supplementary materials.
Studienübersicht
Status
Intervention / Behandlung
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
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-
Ontario
-
Ottawa, Ontario, Kanada, K1H 8L1
- Children's Hospital of Eastern Ontario
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- child with a heart condition requiring on-going follow up between 4 and 17 years of age or parent or healthcare provider of such a child
- able to verbally answer questions and express opinions in English or French
- able to provide informed consent or assent to participate
Exclusion Criteria:
- disability other than heart condition which significantly impacts physical activity participation or healthy lifestyle habits
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Verhütung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Kein Eingriff: Control Group
Receive standard clinical care and supports.
|
|
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Experimental: Supplementary resources
Receive standard care and supports plus supplementary resources developed for the intervention.
|
Clinical and educational resources for patients, their families and the professionals who care for them.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Family perception of clinical service
Zeitfenster: Within 2 weeks of clinic visit
|
Likert scales to measure family satisfaction with healthy lifestyle information and resources provided during clinic visit.
|
Within 2 weeks of clinic visit
|
|
Pediatric Quality of Life Inventory (PedsQL)
Zeitfenster: Within 2 weeks of clinic visit
|
Within 2 weeks of clinic visit
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
|
Change from Baseline of Children's Self-Perceived Adequacy and Predilection for Physical Activity
Zeitfenster: 1 month after intervention completion
|
1 month after intervention completion
|
Andere Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
|
Change from Baseline in Multi-dimension anxiety scale for children
Zeitfenster: 1 month after intervention completion
|
1 month after intervention completion
|
|
Change from Baseline in Pediatric Symptom Checklist
Zeitfenster: 1 month after intervention completion
|
1 month after intervention completion
|
|
Change from Baseline in PedsQL Family Impact Module
Zeitfenster: 1 month after intervention completion
|
1 month after intervention completion
|
Mitarbeiter und Ermittler
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- REB12/04X
- 2012-06-1-4460033 (Andere Zuschuss-/Finanzierungsnummer: Ministry of Health Promotion and Sport Healthy Communities Fund)
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