Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07452107

Effects of a Digital Micro-Movement Nudge Intervention on Well-Being and Academic Outcomes in College Students

The goal of this randomized controlled study is to learn whether a 21-day physical resilience (movement-based) program can improve mental well-being, emotional regulation, and academic functioning in university students.

The main questions it aims to answer are:

Does participation in a 21-day physical resilience program improve students' well-being (e.g., depression, anxiety, stress, affect, life satisfaction, and perceived health)?

Does the program improve students' academic and self-regulatory outcomes (e.g., engagement, burnout, procrastination, productivity, emotion regulation, coping, and self-control capacity)?

Researchers will compare students who complete the physical resilience program immediately to students in a waitlist control group to see whether participation in the program leads to greater improvements in well-being and academic-related outcomes.

Participants will:

Sign up online and provide informed consent

Be randomly assigned to either the intervention group or a waitlist control group

Receive daily micro-movement tasks and reminders via Telegram for 21 days (intervention group)

Complete online questionnaire surveys at baseline, post-intervention, and a 2-week follow-up

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Student of Singapore Management University
  • Uses Telegram

Exclusion criteria

  • Below 18 Years Old

Treatment and study plan

Physical resilience

Behavioral

The intervention is a 21-day, digitally delivered physical resilience program consisting of daily, brief, movement-based activities designed to support mental well-being and academic functioning in university students. The program includes low-intensity physical movement, breathing exercises, and body-based regulation practices that can be completed independently without specialized equipment or prior physical training.

Participants assigned to the intervention group receive one structured movement task per day for 21 consecutive days. Tasks are delivered via a Telegram channel, accompanied by brief digital reminders to prompt engagement. Each task is designed to be short in duration, flexible in timing, and feasible within daily routines, emphasizing consistency rather than physical exertion or performance.

The intervention is self-guided and asynchronous, with no in-person contact, live sessions, or direct supervision.

Other names: Digital Micro-Movement Nudge Intervention

Primary outcomes

  1. State anxiety

    Time frame: Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks

    State anxiety will be assessed using the 6-item Spielberger State-Trait Anxiety Inventory STAI-6 (Marteau & Bekker, 1992). Six items (e.g., "I was worried these past 2 weeks.") rated from 1 (Not at all) to 4 (Very much so) will be averaged for a composite score. Higher scores indicate greater levels of anxiety.

  2. Procrastination

    Time frame: Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks

    Procrastination will be assessed using six items from the Irrational Procrastination Scale (Steel, 2002), such as "At the end of these past 2 weeks, I know I could have spent the time this week better." Participants will respond on a 1-5 scale (1 = Very seldom or not true of me, 5 = Very often true, or true with me), and higher average scores indicate higher levels of procrastination.

Secondary outcomes

  1. Productivity

    Time frame: Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks

    Productivity will be assessed using the Task Performance subscale of the Individual Work Performance Questionnaire (IWPQ; Koopmans et al., 2013, 2014), adapted to the academic context. Participants will respond to five items (e.g., "I was able to plan my work so that I finished it on time") with reference to their schoolwork. Items will be rated on a 6-point scale from 0 (seldom) to 5 (always) and then the scores will be averaged, with higher scores indicating greater productivity.

  2. Study Burnout

    Time frame: Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks

    Study burnout will be measured using the 9-item Study Burnout Inventory (Salmela-Aro & Read, 2017). Participants will indicate how well each item described their experiences (e.g., "I felt a lack of motivation in studying and often think of giving up") on a 6-point scale from 1 (Completely disagree) to 6 (Completely agree). Scores will be averaged, with higher scores indicating greater academic burnout.

  3. Study Engagement

    Time frame: Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks

    Study engagement will be measured using the 9-item Study Engagement Inventory (Salmela-Aro & Read, 2017). Participants will rate items such as "I found studying full of meaning and purpose" based on their experiences. Responses will be given on a 6-point Likert scale ranging from 1 (Completely disagree) to 6 (Completely agree) and higher scores will indicate greater levels of academic engagement.

  4. Implementation intention

    Time frame: Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks

    Implementation intention will be measured using the single item "In the past 14 days, I have taken steps to achieve my goals for the month." scored from 1 (Strongly disagree) to 5 (Strongly agree), where a higher score indicates higher implementation intention.

  5. Goal Progress

    Time frame: Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks

    Goal progress will be measured using the single item "In the past 14 days, I have seen progress towards my goals for the month." scored from 1 (Strongly disagree) to 5 (Strongly agree), where a higher score indicates higher goal progress.

  6. Depression

    Time frame: Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks

    Depression will be measured using an adapted version of the 10-item Short Depression Scale Revised (CES-D-R 10) (Andresen et al., 1994). The scale includes the sample item "I felt that everything I did was an effort." and is scored from 1 (Rarely or none of the time) to 4 (All of the time). Scores will be averaged and higher scores indicate higher risk of depression.

  7. Life Satisfaction

    Time frame: Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks

    Life satisfaction will be measured using an adapted version of Diener's Satisfaction With Life Scale (SWLS). The scale includes 5 items e.g. "In most ways, these past 2 weeks have been close to ideal" and is scored from 1 (Strongly disagree) to 7 (Strongly agree) (Diener et al., 1985). Scores will be summed and higher scores indicate higher life satisfaction.

  8. Perceived Stress

    Time frame: Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks

    Perceived stress will be measured by an adapted version of the 4-item Perceived Stress Scale (PSS) developed by Cohen and colleagues (Cohen et al., 1983). One sample item includes "In the last 2 weeks, how often have you felt difficulties piling up so high that you could not overcome them?" and items are scored from 0 (Never) to 4 (Very often). The composite score is calculated by summing the scores of all items; higher scores indicate higher levels of perceived stress.

  9. Positive and Negative Affect

    Time frame: Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks

    Positive Affect (PA) and Negative Affect (NA) will be evaluated using the Circumplex Model of Affect (Russell, 1980). Participants will rate feelings such as 'Energetic' and 'Dejected' experienced over the past two weeks, from a scale of 1 to 5 (1 = Not at all, 5 = Extremely).

  10. Coping

    Time frame: Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks

    Coping strategies will be assessed using the Brief COPE (Carver, 1997) which is a 28-item self-report measure assessing a range of adaptive and maladaptive coping responses to stress. Participants will indicate how frequently they have engaged in various coping behaviours in response to stress over the past two weeks (e.g., "I've been taking action to try to make the situation better"). Items will be rated on a 4-point scale from 1 (I haven't been doing this at all) to 4 (I've been doing this a lot). Scores will then be averaged for each coping strategy, with higher scores indicating greater use of that coping strategy.

  11. Emotion Regulation

    Time frame: Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks

    Emotion regulation will be assessed using the Emotion Regulation Questionnaire (ERQ; Gross & John, 2003), which is a 10-item self-report measure assessing two emotion regulation strategies: cognitive reappraisal and expressive suppression. Participants will indicate the extent to which they agree with statements describing how they typically regulate their emotions (e.g., "I control my emotions by changing the way I think about the situation I'm in"). Items are rated on a 7-point scale from 1 (strongly disagree) to 7 (strongly agree). Subscale scores will be computed by averaging items corresponding to cognitive reappraisal and expressive suppression, with higher scores indicating greater use of the respective emotion regulation strategy.

  12. Self-Control Capacity

    Time frame: Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks

    Self-control capacity will be assessed using the Brief State Self-Control Capacity Scale (BSSCS; Lindner et al., 2019), which is a 5-item self-report measure assessing individuals' perceived momentary self-control resources. Participants will indicate the extent to which each statement reflects their experiences over the past two weeks (e.g., "I felt like my willpower was gone"). Items are rated on a 7-point scale from 1 (not true) to 7 (very true). Items will be averaged to compute a composite score, with higher scores indicating greater state self-control capacity.

  13. Perceived Health

    Time frame: Enrollment to the end of intervention at 3 weeks and the end of follow-up at 5 weeks

    Perceived health will be assessed using a single-item self-report measure of general health status. Participants will respond to the question, "How would you rate your physical health over the past two weeks?" Responses will be rated on a 5-point scale from 1 (Poor) to 5 (Excellent). Higher scores indicate better perceived physical health.

Study contacts

Contact information is provided by the study sponsor or research team.

Tracy X Chen

CONTACT

[email protected]

+6591691725

Sponsors and collaborators

Lead sponsor

Singapore Management University

Other

Registry information

Official study title

Effects of a Digital Micro-Movement Nudge Intervention on Well-Being and Academic Outcomes in College Students: A Randomized Controlled Trial

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Mar 5, 2026
Registry last updated
Mar 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.