Adapting the ToyBox obesity prevention intervention for use in Scottish preschools : Protocol for a feasibility cluster randomised controlled trial
Malden, Stephen, Hughes, Adrienne R., Gibson, Ann-Marie, Bardid, Farid, Androutsos, Odysseas, De Craemer, Marieke, Manios, Yannis, Summerbell, Carolyn, Cardon, Greet and Reilly, John J.. (2018). Adapting the ToyBox obesity prevention intervention for use in Scottish preschools : Protocol for a feasibility cluster randomised controlled trial. BMJ Open. 8(10), p. Article e023707. https://doi.org/10.1136/bmjopen-2018-023707
|Authors||Malden, Stephen, Hughes, Adrienne R., Gibson, Ann-Marie, Bardid, Farid, Androutsos, Odysseas, De Craemer, Marieke, Manios, Yannis, Summerbell, Carolyn, Cardon, Greet and Reilly, John J.|
Introduction There is an increasing need for the adoption of effective preschool obesity prevention interventions to combat the high levels of early-childhood obesity in the UK. This study will examine the feasibility and acceptability of the adapted version of the ToyBox intervention—a preschool obesity prevention programme—for use in Scotland (ToyBox-Scotland). This will inform the design of a full-scale cluster randomised controlled trial (RCT).
Methods and analysis The ToyBox-Scotland intervention will be evaluated using a feasibility cluster RCT, which involves children aged 3–5 years at six preschools in Glasgow, three randomly assigned to the intervention group and three to the usual-care control group. The original ToyBox intervention was adapted for the Scottish context using a coproduction approach. Within the 18-week intervention, physical activity and sedentary behaviour will be targeted in the preschool through environmental changes to the classroom, physical activity sessions and movement breaks. Parents will receive home activity packs every 3 weeks containing sticker incentives and interactive parent–child games that target sedentary behaviour, physical activity, eating/snacking and water consumption. As this is a feasibility study, parameters such as recruitment rates, attrition rates and SDs of outcome measures will be obtained which will inform a power calculation for a future RCT. Additional variables to be assessed include accelerometer-measured physical activity, sedentary behaviour and sleep, body mass index, home screen time, eating/snacking and water consumption. Outcomes will be assessed at baseline and 14–17 weeks later. Intervention fidelity will be assessed using questionnaires and interviews with parents and practitioners, observation and session delivery records.
Ethics and dissemination This study was granted ethical approval by the University of Strathclyde’s School of Psychological Sciences and Health Ethics Committee. Results will be disseminated through publication in peer-reviewed journals, presentation at conferences and in lay summaries provided to participants.
Trial registration number ISRCTN12831555.
|Journal citation||8 (10), p. Article e023707|
|Publisher||B M J Group|
|Digital Object Identifier (DOI)||https://doi.org/10.1136/bmjopen-2018-023707|
|PubMed Central ID||PMC6224766|
|Open access||Published as ‘gold’ (paid) open access|
|Funder||The Cunningham Trust|
File Access Level
|Online||27 Oct 2018|
|Publication process dates|
|Accepted||20 Sep 2018|
|Deposited||18 Oct 2022|
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