Move@NUS: a Digital Intervention Cohort Promoting Healthy Movement Behaviours

NCT06597890 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2024-09-19

No results posted yet for this study

Summary

The aim of the Move@NUS pilot study is to determine the feasibility of establishing a digital intervention cohort to monitor and improve the health and wellbeing of students by encouraging them to engage in healthy movement behaviours (i.e., physical activity, sleep, and limiting smartphone-based recreational screentime).

The digital intervention cohort consists of:

* 6-months of continuous monitoring of movement behaviours, wellbeing and related factors via an Apple Watch and repeated bursts of ecological momentary assessments (EMAs).
* 3x embedded randomised controlled trials (RCTs) evaluating the efficacy of small-scale smartphone-based interventions designed to nudge participants toward participating in healthier movement behaviours.

Conditions

  • Physical Inactivity
  • Sedentary Behavior
  • Sleep Insufficiency
  • Well-Being, Psychological

Interventions

BEHAVIORAL

educational content (sleep hygiene)

app-based sleep hygiene-related educational content

BEHAVIORAL

sleep hygiene strategies

app-based self-selection of sleep hygiene strategies

BEHAVIORAL

reminders

daily reminders sent via push notifications

BEHAVIORAL

review of behavioural goal

app-based review of behavioural goal

BEHAVIORAL

educational content (sleep guidelines)

app-based educational content on recommended sleep guidelines

BEHAVIORAL

comparison of current behaviour to ideal behaviour

use of smartwatch/smartphone data to assess current behaviour and compare it to ideal behaviour

BEHAVIORAL

goal setting

prompt participant to set a goal in relation to targeted behaviour

BEHAVIORAL

educational content (Vigorous Intermittent Lifestyle Physical Activity (VILPA))

app-based educational content on VILPA

BEHAVIORAL

screentime breaks

repeated daily reminders to break up screentime

Sponsors & Collaborators

Principal Investigators

  • Falk Müller-Riemenschneider, PhD · National University of Singapore

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
25 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-09-09
Primary Completion
2025-02-28
Completion
2025-02-28

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06597890 on ClinicalTrials.gov