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CompletedNCT05854355Updated May 11, 2023

Children- Sit Less, Move More (C-SLAMM): Increasing Physical Activity and Decreasing Sedentary Behaviour in Children

An interventional study of C-SLAMM Study in Physical Inactivity, Sedentary Behavior and Health Behavior, sponsored by University of Ulster. Completed at 1 site in United Kingdom. Open to participants aged 7 Years to 9 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-05-11.

Sponsored by University of Ulster · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 1 year 6 months after the study started (first participant enrolled Sep 2021, registered Mar 2023).
Phase
Not applicable
Study type
Interventional
Enrollment
162
Allocation
Randomized
Ages
7 Years to 9 Years
Sex
All
01

Study summary

The Children Sit Less, Move More (C-SLAMM) study aims to test the feasibility and potential effect of a multi-component school and home-based pilot cluster randomized control trial on reducing sedentary behavior and increasing physical activity in children.

This pilot intervention will be an 8-week two-armed cluster RCT. Individuals (children aged 7-9 years) will be the unit of analysis and schools (cluster) randomly assigned to one of two arms: (1) Physical activity and sedentary behavior (intervention arm), or (2) current practice (control arm). The design conduct and reporting of the intervention with adhere to the Consolidation Standards of Reporting Trials (CONSORT) guidelines and is guided by the Standard Protocol Items for Randomized Trials (SPIRIT) Statement.

Read the detailed description

The C-SLAMM study is an 8-week school-and home-based feasibility, two-armed pilot cluster randomized controlled trial.

A convenience sample of primary schools in Northern Ireland will be invited to take part in the study. Baseline measurements will proceed randomization, and an identical set of measures will be taken from participants in week 8 of the intervention.

Individuals (Primary 4 and Primary 5 children, aged 7-9 years) will be the unit of analysis and schools (clusters) will be randomly assigned to one of two conditions: (1) intervention condition or (2) current practice (control condition). Given the nature of the intervention, blinding of schools and participants will not be possible following randomization. The researcher responsible for subsequent data collection and analysis will not be blinded to group allocation. Any differences between the intervention and control groups will be by chance and adjusted for in the analyses. Schools randomized to control will be offered information on the intervention and associated materials at the end of the intervention.

The intervention is, adapted from the previously tested Transform-Us! trial and informed by a qualitative study was on the perceived barriers and facilitators of physical activity within the classroom, school and/or home environment (REC/20/0033).

The C-SLAMM study will use innovative behavioral, pedological, and environmental strategies within the classroom, school, and home settings to get children moving more and sitting less. Resources include health lessons, active lessons, active breaks, active homework to do with parents, active environments, and newsletters for parents. Each week teachers will be advised to incorporate elements of the intervention within the classroom setting. Teachers will modify the delivery of at least one class lesson per week (\~30 minutes) so that children will complete the lesson standing up. Teachers will be provided with a suite of standing lesson delivery methods that can be modified to any class topic. In addition, every two-hour classroom teaching block will be interrupted every 30 minutes with a 2-minute guided light-intensity activity break. This will equate to a total of six minutes interrupted sitting time every two hours. Furthermore, each class will be provided with six standing desks so that children can rotate learning activities at 'standing stations'. A novelty timer will be given to each class so that teachers can monitor 2-minute standing breaks and every 30-minutes of sitting class time.

To compare the effects of the intervention against usual practice, schools assigned to the control arm will be requested to continue with their usual practice and lesson delivery, no environmental changes will be made to their classrooms. The participants in the control schools will be asked to complete the same study measurements as those in the intervention schools at the same time points.

02

Conditions studied

  • Physical Inactivity
  • Sedentary Behavior
  • Health Behavior
  • Child Behavior
  • Physical Activity
03

In context

Lead sponsor

University of Ulster is the lead sponsor of 94 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
7 Years to 9 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Primary school pupil
  • Year 4 (Key Stage 1) or Year 5 (Key Stage 2)
  • 7-9 years
  • Living in Northern Ireland

Exclusion criteria

Exclusion Criteria:

  • Cannot speak English
  • Severe psychological or neurological condition
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
162 participants (actual)

Study arms

  • Experimental
    Intervention

    This group received the multi-component school and home-based intervention (physical activity programme (aimed to increase children's physical activity and decrease sedentary behaviour)

    Other: C-SLAMM Study

  • No intervention
    Control

    The primary school children in the control group did not receive the intervention. The control arm continued with their usual practice and lesson delivery, no environmental changes were made to their classrooms.

Interventions

  • OtherC-SLAMM Study

    The intervention arm includes using innovative behavioural, pedagogical, and environmental strategies within the classroom, school, and home settings to get children moving more and sitting less. The strategies were based on strategies used in Transform-Us! involved incorporating movement into everyday class lessons - the delivery of the lesson changes, not the content. Resources included health lessons, active lessons, active breaks, active homework to do with parents, active environments, and newsletters for parents.

06

What researchers measure

Primary outcomes

  1. Sitting time (mins)

    Change in time spent sitting using activPAL inclinometer device

    Time frame: 7 days at baseline and at follow-up (8 weeks)

Secondary outcomes

  1. Standing time (mins)

    Change in time spent standing using activPAL inclinometer device

    Time frame: 7 days at baseline and at follow-up (8 weeks)

  2. Stepping time (mins)

    Change in time spent stepping using activPAL inclinometer device

    Time frame: 7 days at baseline and at follow-up (8 weeks)

  3. Steps

    Changes in Steps using activPAL inclinometer device

    Time frame: 7 days at baseline and at follow-up (8 weeks)

  4. Sit to stand transitions

    Changes in Sit to stand transitions using activPAL inclinometer device

    Time frame: 7 days at baseline and at follow-up (8 weeks)

  5. Height (m)

    Change in height measured with portable Stadiometer

    Time frame: 7 days at baseline and at follow-up (8 weeks)

  6. Weight (kg)

    Change in weight measured with electronic weighing scales

    Time frame: 7 days at baseline and at follow-up (8 weeks)

  7. Body Mass index (kg/m2)

    Change in BMI calculated from height and weight measures

    Time frame: 7 days at baseline and at follow-up (8 weeks)

07

Study locations

1 site
  • Ulster University
    Newtownabbey, Co. Antrim BT370QB, United Kingdom
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 11, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05854355
Lead sponsor
University of Ulster
Collaborators
Northern Ireland Chest Heart and Stroke
Responsible party
Sponsor
First posted
May 11, 2023
Start date
Sep 1, 2021
Primary completion
Apr 13, 2022
Completion
Jun 12, 2022
Last update
May 11, 2023

Study contacts

Marie Murphy, PhD
principal investigator · University of Ulster

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2023. You cannot join it, but the record below documents what was studied.

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