- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT01750996
Strongest Families Finland Canada: Family-based Prevention and Treatment Program of Early Childhood Disruptive Behavior (Fin-Can)
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
This project will have two phases, described below. The first part will be development of the web based program, the second part will be the implementation of the program in Finland. All participants will be recruited in Finland and all research activities will take place in Finland, by the Finnish Consortium. The Canadian Consortium will assist in funding and provide expert support.
Part 1: Website development:
The Strongest families program provides evidence based psychological and behavioural interventions to families with children with mild to moderate mental health problems. Parents work through a handbook with exercises, watch instructional videos and participate in weekly phone calls from a trained 'coach' (paraprofessional) to provide support, respond to parents' questions and highlight the skills included in a handbook. The preliminary analysis of a Strongest Families effectiveness trial based at the Izaak Walton Killam Children's Hospital (IWK) Health Centre (Projects #2234, and #2654) and effect size reports from the IWK Strongest families Service Program suggest that Strongest Families is an effective treatment for Oppositional Defiant Disorder (ODD).
Strongest Families is an adaptation of the COPE program. COPE is a large-group parent training program (average 25 families per group) that has been evaluated and used in many centres across Canada, the United States and Europe. It was developed at McMaster University by a team led by Dr. Charles Cunningham (one of the investigators on this submission). The groups use a coping modelling problem solving approach to skill acquisition which encourages parents to discuss the solution to common problems, collaborate in the formulation of child management strategies, share successes, and provide supportive feedback. Large group discussions may also provide more information regarding normal child development and a greater perspective on common child management difficulties than clinic/individual parent training .
The benefits for parents participating in COPE group sessions are many, but the burden of traveling to receive services can impede attendance, especially for families in rural areas. One solution to this issue would be to adapt individualized Strongest Families to a more accessible mode.
We propose to develop a web-based version of Strongest Families in preparation for a Randomized Control Trial (RCT) in Finland. All components of web site will be developed using a collaborative approach with active participation by all members of the research team. We will review each of the component as it is developed. We estimate a minimum of three rounds of testing for each component. The program will be evaluated using the user-interface so that we review the website and all its various features in a manner that simulates the actual parent experience. No qualitative or quantitative data will be recorded for this phase of the project. No participants will be recruited for this phase of the trial.
The web version of Strongest Families will have two components. First, is a personalized website that tracks and uses all activities and interactions to modify the Strongest Families intervention as the user progresses through the sessions. Interactions include questions, surveys, and polls which will be asked periodically throughout the program (for examples see Appendix A). Second, the parenting skills curriculum will be based on our Strongest Families program, an approach derived from programs developed by members of this team18,19. Third, parents , using pseudonyms, will participate in a discussion board/blog to exchange ideas. Pseudonyms will be chosen by the participant, but will not include any identifying elements.
Part 2: Randomized trial (Conducted in Finland, no Canadian recruitment)
The centerpiece project will be a population-based RCT of high risk 4 year olds attending well-child clinics in Turku and environs. Families of children with behavioural challenges fort he last six months, scoring 5 points or more on the Conduct subscale of the Strengths and Difficulties Questionnaire (SDQ) and with some perceived problems by the parent in the impact section of the SDQ will be offered participation in a 2 arm trial. All data will be collected in Finland and stored at the University of Turku. All forms/scripts/ measures will be administered in Finnish or Swedish. This project has been approved by the Intermunicipal Hospital District of Southwest Finland. The Canadian team will provide expert and financial support.
Treatment Group: Families randomized to Web-Enhanced Strongest Families (described above) will receive the website program described above.
Control Group: Families randomized to Educational Control will receive access to a static website with parenting tips as well as a 45 coaching call to review the parenting tips.
Randomization: (1:1 treatment: control; stratified by sex). Randomization sequences were generated by a qualified expert at arms length to the trial using a random permuted block sequence generator then concealed the placements using a double envelop system labeled with sequential numbers. Study staff were blinded to placements until randomization was completed by a study staff delegate.
Studientyp
Einschreibung (Tatsächlich)
Phase
- Phase 2
- Phase 1
Kontakte und Standorte
Studienorte
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TUrku, Finnland
- University of Turku, Finland
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- Child is 4 years old at time of recruitment
- Parent/guardian has access to a computer and the internet
- Parent/guardian is comfortable reading at a Grade 5 level
Child meets screening criteria (SDQ score of 4 or more with some problems per impact score)
- Child has had behavioural challenges for the last 6 months
- Parent has access to phone in home
- Parent speaks/writes Finnish
Exclusion Criteria:
- - Has received or is receiving behavioral treatment (parent training) before
Diagnosis of:
- Autism or a Pervasive development disorder (PDD)
- Down's syndrome
- Fetal Alcohol Syndrome
- Mental retardation
- Genetic diagnosis that will lead to mental retardation
- Major mental health disorder (e.g., depression, psychosis)
- Child is not speaking using a sentence
- Child is deaf or blind
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Verhütung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Verdreifachen
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
---|---|
Kein Eingriff: Usual Care control (Parenting tips)
Participants randomized to usual care will have access to a brief information website containing brief parenting tips but will not receive Strongest Families Intervention
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Experimental: Strongest Families
Strongest Families intervention
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Behavioural intervention
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
CHild Behaviour Checklist (to measure change from baseline)
Zeitfenster: Measure change from baseline at 6 & 12 months
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Measure of child behavioural change from baseline to 6 & 12 months
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Measure change from baseline at 6 & 12 months
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Depression Anxiety and Stress Scale Short Form (DASS-21)- Finnish
Zeitfenster: Baseline, 6 & 12months
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Parental stress changes from baseline will be measured over time
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Baseline, 6 & 12months
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The Parenting Scale (To measure change from baseline to 6 & 21 months)
Zeitfenster: To measure change from baseline to 6 & 12 months post randomization
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Measure parental parenting practice changes from baseline
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To measure change from baseline to 6 & 12 months post randomization
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Barkley's Quick-Screen: The Barkley Adult ADHD Rating Scale IV (to measure change from baseline)
Zeitfenster: Measure change from baseline to 6&12 months
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To measure parental ADHD symptom changes form baseline
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Measure change from baseline to 6&12 months
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Child Behaviour Checklist- Teacher version (to measure change since baseline)
Zeitfenster: Measure change from Baseline to 6 & 12 months
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To measure child behaviour changes at daycare from baseline to 6 & 12 months post randomization
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Measure change from Baseline to 6 & 12 months
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Satisfaction measure: Researcher designed for the Intervention group
Zeitfenster: end of program intervention (average is about 5 months but timing of completion varies between participants.)
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To measure satisfaction with Intervention and website information
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end of program intervention (average is about 5 months but timing of completion varies between participants.)
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Strengths & Difficulties Questionnaire (Screening Tool)
Zeitfenster: Screening
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Screening tool used to identify high risk 4 year olds
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Screening
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The Parent Problem Checklist
Zeitfenster: Measure change from Baseline to 6 & 12 months
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To measure interparental conflict
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Measure change from Baseline to 6 & 12 months
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The Sense of Coherence Scale (SOC-13)
Zeitfenster: Measure change from Baseline to 6 & 12 months
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To measure parent's sense of coherence (i.e., global view of the world, and individual environment as comprehensible, manageable and meaningful)
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Measure change from Baseline to 6 & 12 months
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The Inventory of Callous-Unemotional Traits
Zeitfenster: Measure change from Baseline to 6 & 12 months
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To measure child empathy
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Measure change from Baseline to 6 & 12 months
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Mitarbeiter und Ermittler
Sponsor
Mitarbeiter
Ermittler
- Hauptermittler: Patrick J McGrath, PhD, IWK Health Centre
Publikationen und hilfreiche Links
Allgemeine Veröffentlichungen
- McGrath PJ, Sourander A, Lingley-Pottie P, Ristkari T, Cunningham C, Huttunen J, Filbert K, Aromaa M, Corkum P, Hinkka-Yli-Salomaki S, Kinnunen M, Lampi K, Penttinen A, Sinokki A, Unruh A, Vuorio J, Watters C. Remote population-based intervention for disruptive behavior at age four: study protocol for a randomized trial of Internet-assisted parent training (Strongest Families Finland-Canada). BMC Public Health. 2013 Oct 21;13:985. doi: 10.1186/1471-2458-13-985.
- Sourander A, McGrath PJ, Ristkari T, Cunningham C, Huttunen J, Lingley-Pottie P, Hinkka-Yli-Salomaki S, Kinnunen M, Vuorio J, Sinokki A, Fossum S, Unruh A. Internet-Assisted Parent Training Intervention for Disruptive Behavior in 4-Year-Old Children: A Randomized Clinical Trial. JAMA Psychiatry. 2016 Apr;73(4):378-87. doi: 10.1001/jamapsychiatry.2015.3411.
- Sourander A, Ristkari T, Kurki M, Gilbert S, Hinkka-Yli-Salomaki S, Kinnunen M, Pulkki-Raback L, McGrath PJ. Effectiveness of an Internet-Based and Telephone-Assisted Training for Parents of 4-Year-Old Children With Disruptive Behavior: Implementation Research. J Med Internet Res. 2022 Apr 4;24(4):e27900. doi: 10.2196/27900.
- Sourander A, McGrath PJ, Ristkari T, Cunningham C, Huttunen J, Hinkka-Yli-Salomaki S, Kurki M, Lingley-Pottie P. Two-Year Follow-Up of Internet and Telephone Assisted Parent Training for Disruptive Behavior at Age 4. J Am Acad Child Adolesc Psychiatry. 2018 Sep;57(9):658-668.e1. doi: 10.1016/j.jaac.2018.07.001. Epub 2018 Aug 3.
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
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- CIHR# 103146
Plan für individuelle Teilnehmerdaten (IPD)
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Beschreibung des IPD-Plans
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