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Parent PLAYSHOP: A Physical Literacy Training Workshop for Parents

27. April 2021 aktualisiert von: Valerie Carson, University of Alberta

The objective of this research is to 1) determine the impact of a physical literacy training workshop for parents of preschool children (3-5 years) on their knowledge and confidence levels in regards to engaging in meaningful physical activity with their child(ren) in order to promote physical literacy. 2) Evaluate workshop reach and implementation facilitators and barriers.

In this pilot study, interested participants will be randomized into the intervention group or the wait-list control group. Participants will complete two brief surveys regarding their knowledge and confidence in doing physically activities with their children. The intervention group will receive a 75 minute physical literacy workshop at baseline, and complete a 2 month follow-up interview. The wait-list control group will receive the workshop after questionnaires have been completed.

Statistical analysis will be conducted to compare change in knowledge and confidence levels in between intervention and control groups. Findings will contribute to promoting and improving parental confidence in providing opportunities for children to develop their physical literacy and advance future research regarding physical activity promotion for children.

Studienübersicht

Status

Abgeschlossen

Intervention / Behandlung

Detaillierte Beschreibung

Purpose/objective: 1)Determine if a physical literacy training workshop can increase parental knowledge, confidence levels, and improve parenting practices related to engaging in play with their preschool child(ren) that facilitates the development of physical literacy. 2) Evaluate workshop reach and implementation facilitators and barriers.

Hypothesis: 1)Parents in the intervention group will have a larger increase in parental knowledge and confidence levels in regards to engaging in meaningful play with their preschool child(ren) than parents in the control group. 2) Parents will report satisfaction with the implementation and that they changed parenting practices related to physical activity at the 2 month follow-up.

Justification: Preschoolers are typically at a development stage where they are beginning to possess a unique set of motor skills that allow them to engage in a wider range of physical activities. Parents have been identified as a key gatekeeper for physical activity in children.

Research method: This pilot study is a Type 1 Hybrid Effectiveness Trial, where an intervention is tested while also gathering information on the effectiveness and potential for real world use (Curran et al., 2012). Approximately, 100 participants will be randomized into an intervention group or a wait-list control group across two Canadian data collection sites: Edmonton, Alberta and Victoria, British Columbia. Participants in the intervention group will receive a 75 minute physical literacy workshop in their community (e.g. community recreation centre, local school, family resource centre) at baseline, where their preschool child is encouraged to attend and participate. The workshop will provide parents with physical literacy training including modifications for the home setting.The overall aim of the workshop is to support parents in engaging in play with their child that facilitates the development of physical literacy. The program was designed using Bandura's social cognitive theory (Bandura, 1986) with a specific emphasis on parent's self-efficacy and related intervention change techniques described using the Behavior Change Wheel (BCW; a synthesis of 19 behavior change frameworks). To address the 1st objective, the intervention group will complete a brief pre-workshop questionnaire, post-workshop questionnaire, and a follow-up interview approximately 2 months after the workshop. At the end of the workshop, parents will take home a goody bag with basic and inexpensive play equipment/resources. In between the workshop and the 2 month follow-up, they will receive at least two booster e-mails/texts with play ideas. The wait-list control group will complete the two questionnaires online (approximately 1 week apart) around the same time as the intervention group and receive the workshop at a later date. The control group will also receive the goody bag. To address the 2nd objective, parents will report their satisfaction and facilitators and barriers to implementing activities and research staff/partners that delivered the workshops will be invited to be interviewed at the end of the study in order to evaluate reach and implementation facilitators and barriers .

Plan for data analysis: Repeated measures ANOVA and/or linear mixed models will be used to compare change in knowledge and confidence levels between intervention and wait-list control groups (Objective 1). Thematic analysis will be used to analyze parent's satisfaction and changes in parenting practices reported in the 2 month follow-up interview (Objective 1). Thematic analysis will also be used to evaluate the reach and implementation facilitators and barriers reported by parents and research staff/partners (Objective 2).

Studientyp

Interventionell

Einschreibung (Tatsächlich)

89

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Alberta
      • Edmonton, Alberta, Kanada, T6G 2H9
        • University of Alberta, Van Vliet Complex
    • British Columbia
      • Victoria, British Columbia, Kanada, V8P 5C2
        • University of Victoria, McKinnon Building

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Kind
  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Ja

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  • Parents with a pre-school aged child (3-5 years old)

Exclusion Criteria:

  • Parents that are not comfortable speaking and reading English

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Sonstiges
  • Zuteilung: Nicht randomisiert
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Intervention
Participants will attended a 75 minute physical literacy workshop (Parent PLAYSHOP). A questionnaire will be completed at the beginning of the workshop and the end of the workshop to measure if there is a difference in parent's knowledge and confidence levels in regard to engaging in meaningful physical activity with their children.

The Parent PLAYSHOP includes:

  1. Educational Training- the 75 min workshop will be delivered by a trained facilitator. Parents will be introduced to physical literacy via education, group discussion, and active participation in fundamental movement skills (FMS) based activities. Parents will be provided with modifications to perform activities 'at home'.
  2. Distribution Education and Activity Resources- At the workshop conclusion parents are given education Resources (e.g. Canada's 24-hour movement guidelines for the early years, activity idea booklet, and a physical literacy handout) and inexpensive activity resources (ball, bean bag, scarves, balloons etc.).
  3. Provide Follow-up Support- Research staff will send parents a follow-up email with key workshop messages (e.g., rationale and importance of physical literacy); support and encouragement for parents to engage in purposeful play with their child; and an opportunity for parents to provide feedback and/or seek further support.
Kein Eingriff: Control
Participants will complete the 2 questionnaires online, one week or more apart. Once questionnaires are completed they will be invited to attended the 75 minute physical literacy workshop. The workshop content and delivery will be the same as the intervention group but will not include questionnaires.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Changes in parental knowledge, confidence, and intention in engaging in purposeful play with their preschool child(ren) that builds physical literacy.
Zeitfenster: Before and immediately after the 75 minute workshop
The pre and post workshop questionnaires will assess changes in parent's knowledge and confidence of specific physical literacy components (e.g. manipulative skills, locomotor skills, balance and stability skills) and intention to engage in purposeful play with their preschool child(ren).
Before and immediately after the 75 minute workshop
Changes in parenting practices regarding engagement in purposeful play.
Zeitfenster: Approximately 2 months after attending the workshop
In the semi- structured interview approximately 2 months after the PLAYSHOP, parents will be asked about changes in their parenting practice regarding engagement in meaningful activities with their preschool child(ren) that builds physical literacy.
Approximately 2 months after attending the workshop

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Parental satisfaction and implementation barriers and facilitators.
Zeitfenster: Approximately 2 months after attending the workshop
In the semi- structured interview approximately 2 months after the PLAYSHOP, parents will report their satisfaction with the workshop. Parents will also be asked what facilitators and barriers they have experienced while implementing physical literacy activities in their home since the workshop.
Approximately 2 months after attending the workshop
Intervention reach and workshop implementation barriers and facilitators.
Zeitfenster: After study completion, approximately 6 months from start of project
In the semi-structured interview with research staff/partners, participants will report facilitators and barriers of workshop delivery and proposed changes.
After study completion, approximately 6 months from start of project

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: Patti-Jean Naylor, PhD, University of Victoria
  • Hauptermittler: Valerie L Carson, PhD, University of Alberta

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

27. November 2019

Primärer Abschluss (Tatsächlich)

30. August 2020

Studienabschluss (Tatsächlich)

30. August 2020

Studienanmeldedaten

Zuerst eingereicht

11. Mai 2020

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

14. Mai 2020

Zuerst gepostet (Tatsächlich)

19. Mai 2020

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

29. April 2021

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

27. April 2021

Zuletzt verifiziert

1. April 2021

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • PLAYSHOP

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Beschreibung des IPD-Plans

To protect participant's personal data IPD will not be shared with other researchers.

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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