Reset your password and enable multi-factor authentication (MFA)


For ANZCTR account holders: to help ensure the cyber safety of your account, you’ll need to reset your password and set-up multi-factor authentication (MFA) as per the instructions below.


  1. Go to the Login page, click ‘reset password’ and follow the instructions.
  2. Check your email for the link to set a new password.
  3. Create a new password that meets requirements. New passwords must include at least one lowercase letter, one uppercase letter, one number and one special character (e.g. !#$%&@).
  4. Return to the Login page and enter your new password. A verification code will be sent to your email.
  5. Check your email for the code and enter it on the Login page. If the code is entered incorrectly, you can re-enter the correct one or request a new one.

Learn more about MFA and its importance on the Australian Signals Directorate website.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial registered on ANZCTR


Registration number
ACTRN12625000505404p
Ethics application status
Not yet submitted
Date submitted
23/04/2025
Date registered
22/05/2025
Date last updated
22/05/2025
Date data sharing statement initially provided
22/05/2025
Type of registration
Prospectively registered

Titles & IDs
Public title
Effects of A Sit Less and Move More (SLAMM) App on Sedentary and Physical Activity Behaviours
Scientific title
Effects of A Mobile App-based Sit Less and Move More (SLAMM) Intervention on Sedentary and Physical Activity Behaviours Among Australian Adults
Secondary ID [1] 314263 0
None
Universal Trial Number (UTN)
Trial acronym
SLAMM
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Sedentary Behaviour 337202 0
Physical Inactivity 337203 0
Condition category
Condition code
Public Health 333610 333610 0 0
Other public health

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
A single-arm 12-week digital intervention study will be conducted using a mobile application-based behaviour change platform called SLAMM (Sit Less And Move More). The intervention combines real-time activity tracking with context-aware, semi-personalised behavioural support.

Objectives:
To evaluate the feasibility, usability, and preliminary effects of a progressive digital health intervention aimed at reducing sedentary behaviour (SB) and promoting light-to-moderate physical activity (PA).

Aims:
1- To assess changes in sedentary behaviour and physical activity over 12 weeks.
2- To evaluate user perceptions of feasibility, usability, and acceptability of the SLAMM intervention.
3- To explore how personalised and contextually adapted behavioural strategies influence daily movement behaviour (sitting time, active time, exercise time).

Participants:
Participants will be community-dwelling adults who are at high-, medium-high-, medium- or low-medium risk for cardiovascular health. The risk level is determined via a SIT-ACT risk matrix, which considers sedentary hours and physical activity minutes combined.

Intervention Components:
Participants will be classified into movement behaviour levels (Sit Less, Move More, and Exercise) based on their sedentary and activity levels using a risk assessment tool (i.e. the Sit-Act Matrix). Sit Less Group: receives only Sit Less messages. Move More Group: receives both Sit Less and Move More components. Exercise Group: receives all components, including an exercise program. Participants can progress to a higher group (risk level) on a weekly basis based on their behavioural data captured by the mobile app. Messages include:

- Sit Less: Motivational messages to interrupt sitting, adapted to time of day, weather, and work status.
- Move More: Prompts encouraging walking or light movement integrated with daily routines.
- Exercise: Semi-automated coaching with light-to-moderate intensity exercise prescriptions.

Participants will receive up to six messages per day. These messages are designed to prompt behavioural changes and are data-driven, meaning they are triggered by prolonged sitting periods or relevant activity patterns (moving or exercising). Potential time points will include morning, lunchtime, afternoon and evening,
Examples of messages:
Sit Less: “Stuck inside because of bad weather? Stay active indoors by climbing stairs or pacing between rooms.”
Move More: “Been sitting too much? Break up your day with a lunchtime walk with a coworker.”
Exercise: “Swimming for 40 minutes from 7:00 to 7:40 am; the intensity level: moderate [select via app].”
Exercises prescribed to the Exercise Group include activities such as swimming, or cycling, tailored to light-to-moderate intensity. This will be measured using the Borg Rating of Perceived Exertion (RPE) scale.

Adherence:
Adherence to the intervention will be assessed by interaction with the app (logging activities and app screen time). App analytics will thus provide ongoing monitoring of participant engagement and intervention fidelity.

Technology:
Participants will use the SLAMM mobile app, which integrates with Fitbit or a personal activity tracker to collect real-time movement and sedentary data. The app also accesses contextual data (e.g., weather) to deliver adaptive prompts.

Decision Logic:
Messages are dynamically generated based on participant availability, movement levels, contextual factors, and behavioural trends.

Data Collection:
Objective data will include sedentary hours. activity minutes, exercise minutes, self-reported questionnaires and post-intervention interviews will assess usability, satisfaction, and behavioural awareness.

Sample Size:
A total of 38 community-dwelling adults will be recruited to evaluate preliminary effects and feasibility metrics. Results will guide future iterations and a larger-scale randomised trial.

Recruitment Timeframe:
Start Date: Recruitment is expected to commence in mid-July 2025.
End Date: Recruitment will conclude in early July 2026, or once the target sample size of 38 participants is reached, allowing time for replacements if any participant withdraws.
Intervention code [1] 330876 0
Lifestyle
Comparator / control treatment
No Control Group
Control group
Uncontrolled

Outcomes
Primary outcome [1] 341187 0
Average daily sedentary time (hours)
Timepoint [1] 341187 0
Continuous/ everyday for 12 weeks post-intervention commencement
Primary outcome [2] 341188 0
Average daily physical activity time (minutes)
Timepoint [2] 341188 0
Continuous/ everyday for 12 weeks post-intervention commencement
Primary outcome [3] 341189 0
Average daily exercise time (minutes)
Timepoint [3] 341189 0
Various times during the week for 12 weeks post-intervention commencement (assigned by the participant)
Secondary outcome [1] 446704 0
Participant recruitment rate
Timepoint [1] 446704 0
Post-intervention (week 12)
Secondary outcome [2] 446705 0
Usability
Timepoint [2] 446705 0
Post-intervention (week 12)
Secondary outcome [3] 446706 0
Acceptability
Timepoint [3] 446706 0
Post-intervention (week 12)
Secondary outcome [4] 446707 0
Awareness and perception of behaviour change (composite measure)
Timepoint [4] 446707 0
Post-intervention (week 12)
Secondary outcome [5] 447121 0
retention
Timepoint [5] 447121 0
Post-intervention (Week 12)
Secondary outcome [6] 447695 0
Technical issues
Timepoint [6] 447695 0
Everyday two weeks post-intervention commencement via phone call

Eligibility
Key inclusion criteria
Eligible participants will be Australian adults, aged 20 years or older, own a smartphone (compatible with our app) and currently interact or engage with apps, have no limitation (including physical problems and medical complications) to engage in low-intensity and intensity PA, those who will not be identified to be at low-risk level, having a compatible wearable activity device, can communicate in English, and can provide informed consent.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Individuals who self-report being highly active (low-risk), as well as those unable or fail to provide informed consent, and refuse to grant permission to access built-in mobile weather app will be excluded from the study.

Study design
Purpose of the study
Treatment
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis
Descriptive Statistics:
Participant’s baseline data (e.g., age, BMI, baseline sedentary time) will be summarised using descriptive statistics (mean, median, standard deviation, interquartile range).

Longitudinal Analysis:
Mixed-effects models: changes in sedentary time, overall activity time, and exercise time over 12 weeks will be analysed, accounting for repeated measures within individuals. This model can handle missing data and variability in individual trajectories.

Correlation and Mediation Analysis:
Spearman or Pearson Correlation will be used to investigate relationships between sedentary time, overall activity time, exercise time, risk levels, and awareness and perception of change in sedentary behaviour and physical activity (e.g., have you thought more often about sitting less or moving more?).

Recruitment
Recruitment status
Not yet recruiting
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
ACT,NSW,NT,QLD,SA,TAS,WA,VIC

Funding & Sponsors
Funding source category [1] 318785 0
University
Name [1] 318785 0
Deakin University
Country [1] 318785 0
Australia
Primary sponsor type
University
Name
Deakin University (Institute for Physical Activity and Nutrition)
Address
Country
Australia
Secondary sponsor category [1] 321228 0
None
Name [1] 321228 0
Address [1] 321228 0
Country [1] 321228 0

Ethics approval
Ethics application status
Not yet submitted
Ethics committee name [1] 317393 0
Deakin University Human Research Ethics Committee (DUHREC)
Ethics committee address [1] 317393 0
Ethics committee country [1] 317393 0
Australia
Date submitted for ethics approval [1] 317393 0
28/05/2025
Approval date [1] 317393 0
Ethics approval number [1] 317393 0

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 140914 0
Prof Ralph Maddison
Address 140914 0
221 Burwood Highway Burwood Victoria 3125 Institute for Physical Activity and Nutrition Deakin University
Country 140914 0
Australia
Phone 140914 0
+61392446218
Fax 140914 0
Email 140914 0
Contact person for public queries
Name 140915 0
Reza Daryabeygikhotbehsara
Address 140915 0
221 Burwood Highway Burwood Victoria 3125 Institute for Physical Activity and Nutrition Deakin University
Country 140915 0
Australia
Phone 140915 0
+61392446108
Fax 140915 0
Email 140915 0
Contact person for scientific queries
Name 140916 0
Reza Daryabeygikhotbehsara
Address 140916 0
221 Burwood Highway Burwood Victoria 3125 Institute for Physical Activity and Nutrition Deakin University
Country 140916 0
Australia
Phone 140916 0
+61392446108
Fax 140916 0
Email 140916 0

Data sharing statement
Will the study consider sharing individual participant data?
Yes
Will there be any conditions when requesting access to individual participant data?
Persons/groups eligible to request access:
Researchers
Conditions for requesting access:
Yes, conditions apply:
Requires approval by an ethics committee
What individual participant data might be shared?
De-identified individual participant data:
All outcomes data
Published results
Primary outcome(s)
What types of analyses could be done with individual participant data?
Systematic reviews and meta-analyses
Studies exploring new research questions
Health economic analyses
Studies testing whether findings can be repeated or confirmed
When can requests for individual participant data be made (start and end dates)?
From:
At the end of the study
To:
A finite period of: 15 years
Where can requests to access individual participant data be made, or data be obtained directly?
Email of trial custodian, sponsor or committee: Prof Ralph Maddison ([email protected])

Are there extra considerations when requesting access to individual participant data?
No


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.