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Happy Homework 2.0: Effects on 24-hour Movement Behaviours in Children

1 de junho de 2026 atualizado por: April Forrest, University of the West of Scotland

Happy Homework 2.0: Effects on 24-hour Movement Behaviours in Children - Findings From a Pilot Cluster Randomised Controlled Trial

The aim of this research is to trial a new version of Happy Homework (HH) on children and parent health outcomes. HH was previously a paper-based 8-week program designed to encourage positive eating habits, physical activity, and healthy sleep routines among children at home. By working together, investigators are aiming make sure HH is easy to use, that it reduces teachers' workload, and enable the students to easily track and engage with HH. We also hope that this will all help contribute to the students meeting 24-hour movement behaviour targets.

Children are invited to participate in the research study. In the study investigators are going to examine children's activity behaviour profiles, and the following measures will be taken:

  • Physical activity levels
  • Sedentary behaviours
  • Sleep duration
  • Body mass index (which can be self-reported by the child).

These measures will be conducted at two time-points; (1) 1 week before the intervention begins and (2) 1 week after the intervention. Should children agree to participate in the study; children will wear an accelerometer on their non-dominant wrist and a small device on their right thigh for 8 consecutive days at both time points, along with having their height and weight recorded (the child can self-report this information).

Visão geral do estudo

Status

Concluído

Condições

Intervenção / Tratamento

Descrição detalhada

The purpose of this study is to implement a new version of Happy Homework (HH). Within this study the HH app will be trialled, using a cluster-randomised control trial (cluster-RCT) design, to determine its effectiveness, feasibility, and acceptability upon child health outcomes, underpinned by the 24-hour movement guidelines. HH was previously an 8-week school-based home-focussed intervention centred on the promotion of primary school children's positive dietary habits, engagement in physical activity (PA) and sleep behaviours.

The cluster- RCT will recruit 4 primary schools in South Lanarkshire (2 control and 2 intervention), with one class of children from each school recruited (n = 30 approx.). During prior co-design workshops, and from findings of an ongoing study, stakeholders (teachers, parents, and children) will help determine the duration of the homework tasks, their frequency, their contents, and the design of the app. Additionally, they will provide opinion on the duration of intervention however, it will be for a minimum of 8 weeks and no longer than 12 weeks. As such, the HH app will include up to 12 weeks of homework tasks to be completed by the children. Reminders to remain active for the remaining weekdays and weekend days will be included to encourage habitual health behaviours. Children will be measured at two points during this period: pre-intervention (1-week prior to intervention delivery) and post intervention (1 week after the intervention).

Measures within the cluster-RCT include demographic information, body mass, physical activity, sedentary behaviour and sleep.

Tipo de estudo

Intervencional

Inscrição (Real)

82

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • South Lanarkshire
      • Blantyre, South Lanarkshire, Reino Unido, G720LH
        • The University of the West of Scotland

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Filho

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion Criteria:

  • children aged 8-12 years old. Hold the ability to carry out homework tasks via digital platform, mostly independently.

Exclusion Criteria:

  • children outwith the age range.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Prevenção
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Triplo

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Happy Homework Arm
The participants randomised to receive the Happy Homework intervention.
Group to receive the Happy Homework 2.0 intervention which assessed physical activity, sedentary behaviour and sleep.
Outros nomes:
  • HH
Sem intervenção: Control arm
Group continue on as normal receiving no intervention.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Feasibility of the Happy Homework 2.0 App
Prazo: Baseline and 8 weeks.
The feasibility of the program was evaluated through recruitment, retention and attrition rates. Recruitment rate was equated by calculating the percentage of children present at baseline testing out of those who were eligible at participating schools. Attrition rate was estimated by analysing the overall drop-out rate, and differences between the control and intervention groups at post-intervention.
Baseline and 8 weeks.
Usability of the Happy Homework 2.0 App
Prazo: Tracked from baseline to 8 weeks.
Usability was measured via uptake and engagement of the HH 2.0 activities tracked via Google analytics.
Tracked from baseline to 8 weeks.
Acceptability of the Happy Homework 2.0 App
Prazo: Tracked from baseline to 8 weeks.
Intervention acceptability was computed by considering HH activity completion. Completion rate of activities was recorded within the HH app.
Tracked from baseline to 8 weeks.
Acceptability of the Happy Homework 2.0 App
Prazo: At 8 weeks.
Acceptability was further evaluated through post-intervention feedback questionnaires provided to participating children, their parents/carers and classroom teachers. Items capturing perception of engagement, usability and areas for improvement were gathered using a 5-point Likert scale, with two open-text statements also included. The Likert scale was based on 1 (strongly disagree) to 5 (strongly agree), with three different variations used for teachers, parents and children to ensure appropriateness and contextual relevance.
At 8 weeks.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
To assess the efficacy of the Happy Homework 2.0 app for improving 24-hour movement behaviours - physical activity.
Prazo: At baseline and again at 8 weeks.
Using an actiPAL 4 monitor, physical activity (MVPA, stepping time, step count) was measured.
At baseline and again at 8 weeks.
To assess the efficacy of the Happy Homework 2.0 app for improving 24-hour movement behaviours - sedentary behaviour.
Prazo: At baseline and again at 8 weeks.
Using an actiPAL 4 monitor sedentary behaviour (sit-to-stand transitions, sitting time, sedentary time, standing time) was measured.
At baseline and again at 8 weeks.
To assess the efficacy of the Happy Homework 2.0 app for improving 24-hour movement behaviours - sleep.
Prazo: At baseline and again at 8 weeks.
Using an actiPAL 4 monitor sleep (sleep duration) was measured. Children were also asked to record sleep and wake times as a method of self-reported sleep duration.
At baseline and again at 8 weeks.
To examine the efficacy of the Happy Homework 2.0 app in changing levels of motivation via basic psychological need satisfaction.
Prazo: At baseline and again at 8 weeks.
Changes in motivation were measured through changes in basic psychological need satisfaction via questionnaires. Questions were taken and adapted from established scales as there was no single validated questionnaire available. A fourteen-item questionnaire was used containing a 5-point Likert scale, based on 1 (really untrue) to 5 (really true) for children to complete.
At baseline and again at 8 weeks.

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

19 de março de 2025

Conclusão Primária (Real)

10 de dezembro de 2025

Conclusão do estudo (Real)

10 de dezembro de 2025

Datas de inscrição no estudo

Enviado pela primeira vez

20 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

1 de junho de 2026

Primeira postagem (Real)

8 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

8 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

1 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Descrição do plano IPD

For ethical and data protection reasons.

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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